PART 1: Slaying Two Dragons with One Stone – How to Prevent Cancer and Aging with the Same Strategy

Two-Headed Dragon iOS

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By James Watson and Vince Giuliano

This is the first part of a three-part series of blog entries on the epigenetic’s of cancer and aging and how those two deadly dragons can be seriously slow down or stopped with the assistance of plant polyphenols. This Part 1 blog entry will 1. Identify similarities in the biological processes and epigenetic’s of cancer and aging, 2.  Identify therefore how common strategies might be found that address both cancer and aging.  3.  Describe the process of Xenohormesis whereby stress response chemicals developed over millions of years in plants keep plants healthy can do the same in humans. 4. Provide molecular explanations for the “causality” of cancer and aging, 5.  Describe the processes in cancer and aging of epigenetic silencing of “good” genes and epigenetic activation of “bad” genes, 6. Identify a 3 tiered “Pyramid” approach for chemoprevention of aging and cancer, 7. Identify the exact interventions involved in each layer of the Pyramid, and 8. Identify how the interventions in the three layers of the Pyramid can be integrated together.

The Part 1 blog entry contains the main messages and the materials in the Part 2 and Part 3 blog entries in this Two-Dragon series provide additional detail, essentially defining a series of appendices to the Part 1entry, They’re published separately because of blog length considerations and because they are of interest in their own right.  The Part 2 blog entry is concerned in more detail with the silencing of good genes in aging and cancer and how many plant polyphenols can prevent that. The Part 3 blog entry is concerned with a. the “unsilencing of bad genes” with sirtuin decline and the harmful results in aging and cancer, and B. providing a master list of drugs and natural compounds for cancer chemoprevention.

The High Lifetime Risk of Cancer occurrence: 43% in males, 38% in females   death risk: 1:4 for males, 1:5 for females

According to the most recent data from US National Cancer Institute’s SEER database, the lifetime risk of developing cancer is 44.81% in males and 38.17% in females.  This is higher than for any other disease except for the age-related diseases (described below). The risk of dying from cancer is 1 in 4 for males and 1 in 5 for females.  This results in a large number of “lost years” due to premature death.  For this reason, developing a cancer risk reduction program should be seriously pursued in a similar fashion to the successful cardiovascular risk reduction programs that have resulted in a dramatic increase in survival over the past 30 years (diet, exercise, statins, anti-platelet therapy, ACE inhibitors, β-blockers, fish oil, and ATreceptor blockers).  Unfortunately, very little chemoprevention has entered clinical practice.

The “Missing Causality” of Cancer cancer etiology:  Genetic causes + Environmental causes + Lifestyle causes 100%

Many causes for cancer have been discovered, based on the study of genetics, epidemiology, toxicology, mutagenesis, and radiation biology.  This has led to the discovery of many risk factors for cancer including inherited mutations, single nucleotide polymorphisms, environmental pollutants, ionizing radiation, UV light, etc.  Despite an extensive study of the genetic and environmental causes of cancer, the evidence suggests that lifestyle factors play a greater role in the etiology of cancer than all genetic and environmental causes combined.  These lifestyle factors include smoking, obesity, sedentary lifestyle, high fat diet, low consumption of fruits and vegetables, alcohol consumption, red meat consumption, and hormone replacement therapy.   When these genetic, environmental, and lifestyle risk factors are mathematically quantified, however, they do not add up to 100%. For most cancers, these 3 categories account for less than 50% of the total cases.  For instance, with breast cancer, inherited gene mutations account for less than 5% of the total cases;  environmental risk factors account for less than 10% of cases; and lifestyle factors account for an estimated 30% of the total cases, which only add up to 40-45%.  Adding the contribution of single nucleotide polymorphisms (SNPs) that increase “gene-determined cancer susceptibility”, we can only account for 50% of the “cause” of breast cancer. What is missing ?  Most believe it is epigenetics.

The High Lifetime Risk of Aging & Age-related diseasesaging etiology: Genetic causes + Environmental causes + Lifestyle causes 100%

The only category of diseases with a higher lifetime risk than cancer is aging and age-related diseases.  Age-related diseases include both those recognized as “formal diseases” by the FDA (cataracts, AMD, osteoporosis, Alzheimer’s disease, osteoarthritis, hearing loss, etc.) and those that are still unrecognized as “formal diseases” by the FDA (skin aging, sarcopenia, osteopenia, fat atrophy, and aging in general).  Obviously, the incidence of aging is 100% and the incidence of these age-related diseases approaches 100% as one ages, but the time of onset varies greatly due to various factors.  Part of the etiology of aging and age-related diseases is known and includes genetic mutations that predispose a person to premature aging (Hutchinson-Gilford progeria, Progeroid syndromes, Werner’s syndrome, Ataxia-Telangiectasia, etc.), environmental factors (UV light exposure, XRT, toxins), and lifestyle factors (obesity, smoking, lack of exercise, alcohol consumption, hormone use, high fat diet, etc.).  Much like cancer, however, these known causes of aging do not add up to 100%.  This again begs the question – “What is missing”. Most believe that it is epigenetics.

The “Missing Causality” of Aging

Many explanations for aging have been proposed, based on the study of model organisms, accelerated aging diseases, knock-out models, exceptionally long-lived organisms, and transgenic model organisms.  Genetic and epigenetic studies have also revealed many more clues. Despite all this data, well over a dozen major theories of aging persist, all of which do not completely explain the findings. You can, for example, see the descriptions of 17 such theories in Vince’s treatise ANTI-AGING FIREWALLS – THE SCIENCE AND TECHNOLOGY OF LONGEVITY.

In an attempt to sort out the causes of aging, the terms “intrinsic aging” and “extrinsic aging” have been coined.  Extrinsic aging includes factors that are due to external, environmental causes such as UV light, radiation exposure, obesity, smoking, dietary factors, and toxins.  Intrinsic aging describes events that occur within a cell that are not due to external factors. Intrinsic aging is the area where most researchers believe the answers to the “missing causality” of both cancer and aging will be found. One of the most effective tools to study intrinsic aging has been the study of Caloric restriction (CR)(ref)(ref).  CR has shown a longevity effect and a health benefit in all organisms except for primates, where CR improves healthspan but may not increase lifespan. CR appears to be a series of adaptive responses to nutritional deprivation where 5 major stress-coping pathways are involved [ (-)mTOR, (-)Insulin/IGF-1, (+) AMPK, (+)SIRT, (+)Autophagy, (+)Mitochondrial biogenesis, (+) ribosome biosynthesis, (-) inflammation].  Other cellular stress adaptation pathways not involved with CR have been identified that confer a longevity advantage as well (electrophile response, xenobiotic response, hypoxia response, unfolded protein response, heat shock response, cold shock response, and the DNA damage response).  A robust adaptive response to all of these stressors is associated with longevity and health.  Several other blog entries have discussed this adaptive response phenomenon known as hormesis(ref)(ref). Unfortunately, the response to all these stressors declines with aging.  Evidence is slowly accumulating, suggesting that epigenetic silencing of important gerosuppresor genes and stress coping genes is the cause.

Cellular Senescence a cellular explanation for aging,& its paradoxic effects on cancer: Good: cancer tumor suppressor mechanism Bad: a cancer promoting mechanism via SASP

The discovery that chromosomes have non-coding DNA “caps” called telomeres at their ends and that telomeres shorten with cell division led to the theory that telomeres were like an “aging clock” with a finite number of ticks on the clock.  The study of telomere shortening led to the discovery of another phenomena called cellular senescence (CS). Senescent cells displayed all the classic signs of aging and telomere shortening was once hailed as the central cause.  Unfortunately, the telomere shortening theory fell apart when other causes of CS were discovered that were independent of telomere length. (See the discussion in the aforementioned  treatise under the subheading An evolving perspective on the Telomere shortening theory of aging and also the discussion in this blog entry.)  CS (not telomere shortening) is now considered to be a central cause of aging and a tumor suppressor mechanism used to turn the cell cycle off in cancer cells(ref).  CS also explains how chemotherapy and radiation therapy can successfully treat cancer by inducing CS, without killing all of the cancer cells.  The beneficial effects of CS in halting the development of cancer and its role in wound healing are the two prime reasons why we do not want to abolish CS pathways.  On the other hand, getting rid of senescent cells would be a good thing for preventing aging and preventing the recurrence of inflammation-driven cancers, since senescent cells are the source of these inflammatory cytokines (the SASP) that drive the epithelial-to-mesenchymal transition, which is a key step in carcinogenesis(ref). This is the paradoxical effect of CS.

The “Two Dragons” are More alike than they are Different – cancer and aging share more similarities than differences

Although there are major differences between aging and cancer, they both end up on the same “dead end” street!  From a proliferative point of view, they are clearly opposites.

Cancer phenotypes all manifested an uncontrolled cell cycle and uncontrolled growth. Aging phenotypes are manifested as cellular senescence, which is “cell cycle arrest”.  In most other aspects, however, cancer cells and senescent cells are actually very similar. Here is a list of some of these similarities:

Cellular   Phenomena Cancer   Cells Senescent   Cells
Inflammation upregulated upregulated
Apoptosis apoptosis resistant apoptosis resistant
Telomeres short short
Inflammation high high
Mitochondria damaged damaged
Reactive oxygen species high levels high levels
Antioxidant enzymes upregulated yes yes
Inflammatory cytokine secretion yes – IL-6 driven yes – IL-6 driven (SASP)
Immune evasion yes –TGF-β driven yes – TGF-β driven
Defective DNA repair yes yes
DNA mutations present present
Harmful epigenetic silencing yes yes
Harmful epigenetic desilencing yes yes
mTOR upregulated yes yes
Ras/Raf pathway upregulated yes yes
c-myc pathway upregulated yes yes
Angiogenesis upregulated yes yes
Extracellular   matrix degradation upregulated Upregulated

You can also check out the discussion in the 2011 publication Cellular senescence: A link between cancer and age-related degenerative disease?

Finding Common Solutions to the Problem of Aging and Canceravoiding strategies with antagonistic pleiotropy effects

How To Kill Two Dragons with One Stone

Interventions that both prevent cancer and aging would be the most effective therapy for increasing average lifespan. Proposed therapies that would fit into this portion of the overlapping circles would include mTOR inhibition, inhibition of the     Insulin/IGF-1 pathway, and inhibition of inflammatory pathways (NF-kB, COX, LOX, etc.). Activating the following pathways would also reduce cancer and increase longevity: AMPK , FOXO, Nrf2, PGC-1a, autophagy, ribosomal biosynthesis, nuclear laminin maintenance, DNA repair pathways, and     epigenetic mechanisms that maintain normal gene expression (DNMT inhibition, HDAC inhibition, HAT inhibition, miRNA maintenance, chromatin  maintenance in the euchromatin state, and preventing epigenetic drift).  Clearing senescent cells and maintaining healthy/normal numbers of stem cells would also solve both.

If cancer and aging have more similarities than differences, there is reason to believe that many strategies that prevent aging could also prevent cancer. Since 20-25% of humans will die of cancer, overall average life span would also be dramatically increased with the reduction of cancer occurrence, even if the maximum life span did not increase with these strategies.  There are many other therapies that may decrease cancer, but that also increase aging.  Examples of this would be the typical treatment for cancer – chemotherapy and radiation. Both of these therapies have been shown to accelerate aging.  Likewise, there are therapies that may be considered “anti-aging”, but increase cancer risk.  This includes the use of exogenous hormone supplementation.  Although certain hormones like HGH appear to reverse some of the undesirable effects of aging, such as muscle atrophy, such hormone supplementation in old age can actually accelerate aging and increase the risk of cancer.  Telomerase activators may have the same effects.  They may decrease cellular senescence but increase cancer in rodents.  For this reason, we propose that anti-cancer therapies and anti-aging therapies can be best understood by the following Venn diagram:


The Concept of Xenohormesis

Xenohormesis is the concept that different species such as plants and animals have common stress signaling molecules, and that such molecules can be harvested from plants and used to increase stress adaptation pathways in animals(ref)(ref)(ref).  Plants cannot run away from predators, parasites, infectious agents, hot weather, or cold weather.  For this reason, plants have evolved a large number of molecular stress coping pathways that are activated by compounds that are actively synthesized in response to the stressor.  Some of these compounds ward off predators with bitter tasting compounds. Others ward off potential organisms that would eat the plant by synthesizing poisons that would kill the predator (i.e. natural pesticides).  Although there are many toxic compounds in this arsenal of phytochemicals, there is a large family of molecules called polyphenols that are non-toxic and appear to have great benefits in humans. Approximately 14,000 of these plant-based stress-signaler polyphenol compounds have been discovered so far in plants.  They are found in the leaves, stems, flowers, seeds, fruits, nuts, and shells surrounding the nuts.  These plant polyphenols appear to be xenohormetic compounds in that they also upregulate stress coping pathways in mammalian cells.  These xenohormetic compounds appear to prevent aging and cancer through a large number of pathways.  For this reason, their mechanism of action is multifactorial or pleiotropic.  Xenohormetic compounds include resveratrol, curcumin, EGCG, isothiocyanates, secoiridoids, genistein, gallic acid, lycopene, allyl mercaptan, plumbagin, etc. Multiple plant polyphenols and their mechanisms of action have been reviewed in past entries in this blog.  See for example ref, ref, ref, ref, ref, ref, ref and ref.xenohormesis1

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Direct Modulation of Key Mammalian Enzymes by Plant Metabolites 

A surprising number of plant molecules in our diet interact with key regulators of mammalian physiology to provide health benefits. Shown are three examples: resveratrol found in numerous plants and concentrated in red wine; curcumin from turmeric; and epigallocatechin-3-gallate (EGCG) in green tea. These compounds modulate key pathways that control inflammation, the energy status of cells, and cellular stress responses in a way that is predicted to increase health and survival of the organism. Such observations raise the question, are these biochemical interactions merely a remnant of what existed in the common ancestor of plants and animals, or is selection maintaining interactions between the molecules of plants and animals? Some interactions activate signaling pathways (arrows) whereas others inhibit them (bars). Solid arrows or bars indicate instances where there is some evidence of a direct interaction of the plant metabolite with a mammalian protein(ref)”A mechanism of xenohormesis appears to be animal gene regulation mediated by plant micro RNAs acquired through food intake.

The 2011 publication Exogenous plant MIR168a specifically targets mammalian LDLRAP1: evidence of cross-kingdom regulation by microRNA reports: “Here, we report the surprising finding that exogenous plant miRNAs are present in the sera and tissues of various animals and that these exogenous plant miRNAs are primarily acquired orally, through food intake. MIR168a is abundant in rice and is one of the most highly enriched exogenous plant miRNAs in the sera of Chinese subjects. Functional studies in vitro and in vivo demonstrated that MIR168a could bind to the human/mouse low-density lipoprotein receptor adapter protein 1 (LDLRAP1) mRNA, inhibit LDLRAP1 expression in liver, and consequently decrease LDL removal from mouse plasma. These findings demonstrate that exogenous plant miRNAs in food can regulate the expression of target genes in mammals.”  The miRNAs are present in microvesicles in the plasma where they are circulated to various cell types and serve as intercellular signaling molecules.  “Our further studies demonstrated that miRNAs could be selectively packaged into MVs and actively delivered into recipient cells where the exogenous miRNAs can regulate target gene expression and recipient cell function15. Thus, secreted miRNAs can serve as a novel class of signaling molecules in mediating intercellular communication15. The novel and important functions of the secreted miRNAs were also reported by many other groups18,19,20,21. The identification of circulating miRNAs, mainly delivered by cell-secreted MVs, as stable and active signaling molecules opens a new field of research in intercellular and interorganelle signal transduction.”

From a 2011 article in The Scientist about this research Plant RNAs Found in Mammals: “To test his hypothesis, Zhang and his team of researchers sequenced the blood microRNAs of 31 healthy Chinese subjects and searched for the presence of plant microRNAs. Because plant microRNAs are structurally different from those of mammals, they react differently to oxidizing agents, and the researchers were able to differentiate the two by treating them with sodium periodate, which oxidizes mammal but not plant microRNAs. — To their surprise, they found about 40 types of plant microRNAs circulating in the subjects’ blood—some of which were found in concentrations that were comparable to major endogenous human microRNAs. — The plant microRNAs with the highest concentrations were MIR156a and MIR168a, both of which are known to be enriched in rice and cruciferous vegetables such as cauliflower, cabbage, and broccoli. Furthermore, the researchers detected the two microRNAs in the blood, lungs, small intestine, and livers of mice, in variable concentrations that significantly increased after the mice were fed raw rice (although cooked rice was also shown to contain intact MIR168a). — Next, the researchers scoured sequence databases for putative target genes of MIR156a and MIR168a and found that MIR168a shared sequence complementarity with approximately 50 mammalian genes. The most highly conserved of these sequences across the animal kingdom was the exon 4 of the low-density lipoprotein receptor adapter protein 1 gene (LDLRAP1).”So, stress-responsive phytochemicals consumed by humans activate similar evolutionary-conserved stress pathways in mammals, including us. “The exogenous mature plant miRNAs in food can pass through mouse GI tract and enter the sera and organs” and “Plant miRNAs execute their function in mammalian cells in a fashion of mammalian miRNA(ref).” The plant’s hormetic-acting chemical stress protection mechanisms developed over millions of years become part of ours.

Molecular Explanations for the “Causality” of Cancer and Aging

Since genetic studies of inherited cancer, genome-wide association studies, epidemiology studies, toxicology studies, and other approaches to studying “causality” have failed to mathematically account for the entire incidence of cancer, a “ground up” investigation of carcinogensis has yielded a plethora of explanations for cancer “causality”.  Most of this has been done with in vitro studies of cancer cells, where they are exposed to various synthetic and natural compounds that activate/inhibit a specific molecular pathway. This has resulted in the discovery of the following molecular explanations for cancer.  These pathways overlap, intersect, or merge at various points.  For this reason, this list should not be viewed as separate mechanisms of tumorigenesis, but rather, different ways of explaining the same phenomena – cancer.  Cancer embodies all of these cellular defects which result in uncontrolled cell division, apoptosis resistance, dependence1.

Epigenetic Silencing of “Good Genes” 

We now know that in many cases, a DNA mutation does not have to occur for cancer to develop.  Instead, the non-mutated gene can be silenced by an epigenetic mechanism that involves histone protein deacetylation of active genes (euchromatin), as well as DNA methylation of cytosine residues at “start sites” on the gene (the “start site” is called the promoter site).  The combination of histone deacetylation and promoter site DNA methylation results in the inability of a transcription factor to access the gene and to bind to the promoter site.  With cancer, over 600 genes have been found to be silenced  by this epigenetic mechanism.  Here is an illustration showing the 6 groups of genes that if silenced, the cell can form cancer without any DNA mutations.  The mechanisms of silencing are the same as that seen in aging.


The Six Hallmarks of Cancer (And why DNA sequencing is not enough to Diagnose the Defects in Cancer) 

Cancer is often thought of as just being a cell that will not stop dividing, a cell that has lost control over the cell cycle.  This is true, but there are actually 6 key features of cancer, and cell cycle control is only one of these. The diagram lists these 6 characteristics of cancer cells and the abbreviations of specific genes that if silenced, allow the cell to turn into cancer.  All of these genes have been identified in various cancers to be silenced or mutated, however they do not all have to be silenced or mutated for the cell to turn into cancer.  Only 1 or 2 of these genes in each category must be silenced or mutated.  Silencing usually occurs due to promoter site (CpG island) methylation, but only 50% of genes have CpG islands. All genes can be epigenetically silenced by histone deacetylation, however. Another form of gene silencing is called polycomb protein silencing.  Another form of silencing involves non-coding RNA called miRNA which prevent the translation of messenger RNA or increase the degradation of mRNA.  DNA mutations also effectively turn off these genes, but mutations do not account for the number of cellular changes seen with cancer.  This is why gene sequencing of cancer cells does not always reveal what genes are not working.  The only way to truly figure this out is to do gene sequencing, epigenetic sequencing, and RNA profiling of cancer.

Examples of Epigenetic Silencing

 1a.     DNA repair gene inactivation by epigenetic silencing – Four examples of this are the genes hMLH1, MGMT, WRN, and BRCA1h.

MLH1 – this an important gene for DNA mismatch repair, which is the way that microsatellite-unstable regions are repaired to avoid them becoming bigger.  Gene inactivation by CpG island hypermethylation has been observed at the promoter site for this gene

MGMT – this is an important gene for fixing mutant guanine bases that become chemically modified by a methyl or alkyl group.  This modification results in the “G” being read as a “A” (i.e. creating a G-to-A single nucleotide polymorphism).  MGMT removes the promutagenic guanine residue.  Unfortunately, this gene is inactivated by CpG island hypermetylation with aging.

WRN – this is the gene responsible for Werner’s syndrome.  This gene codes for the WRN protein which has helicase and exonuclease activity.  With aging, the CpG island at the promoter site for this gene is hypermethylated, effectively silencing this gene.  As a consequence, the manifestations are a progeroid phenotype and increased risk of cancer due to extreme sensitivity to DNA damaging drugs or toxins.

BRCA1 – this gene is the most common gene that is mutated with hereditary breast cancer.  However in sporadic cases of breast and ovarian cancer, the BRCA1gene can be silenced by CpG island hypermethylation in the promoter site of this gene.

b.     Progeroid syndromes and atypical Werner’s syndrome inactivation by epigenetic silencing. Two examples of accelerated aging genes – Lamin A/C and WRN.

Laminin A/C – Mutations in the Laminin A/C gene produce a syndrome called Hutchinson’s- Gilford progeria.  Although most progeroid syndromes are due to DNA      mutations, we now know that a progeroid-like phenomena can be acquired due to epigenetic silencing of the same gene that is mutated in the hereditary              form of HG progeria.  The Laminin A/C gene codes for two different laminin proteins that make up the scaffolding just inside the nuclear double membrane.  When this gene is hypermethylated at the promoter site, a syndrome called “atypical Werner’s syndrome” occurs.

WRN – again, this is called the “Werner gene” and is mutated in classic Werner’s syndrome (WS).  Patients with WS develop accelerated aging and manifest cataracts, type II diabetes, osteoporosis, arteriosclerosis, and cancer at an earlier age and at increased incidence.  There are cases of WS where the only problem is CpG island hypermethylation at the promoter site site.  Again, this is indicative of a need for a “DNA methylome” for proper diagnosis.

1c.     Alzheimer’s disease – Gene inactivation by epigenetic silencing

2. Global hypomethylation of the genome – This is also a feature of cancer and aging that is responsible for activating endoparasitic DNA (i.e. retrotransposons).   This results in global genomic instability, which leads to DNA mutations, cancer, and age-related diseases.

3. Decline in NAD+ Redox Sensors (Sirtuin Deacetylases

a.  Nuclear Effects of Sirtuin Decline: Epigenetic  expression of genes that should be silenced (rDNA locus) – 20 to of SIRT2 & SIRT6 histone deacetylation

Normal Gene silencing

SIRT2 – global deacetylation of lysine 16 on H4  gene silencing –  tenovin-6 inhibits this silencing  genes expressed that should be silenced

SIRT6 – global deacetylation of lysine 9 and 14 on H3  genes silencing – tenovin 6 inhibits this silencing  genes expressed that should be silenced

Consequence of age-induced loss of gene silencing:

rDNA repeat recombination  accumulation of extrachromosomal rDNA circles, aging or cell death

telomeres are not silenced

b.  Cytoplasmic Effects of Sirtuin Decline:  gene expression for stress resistance and cancer prevention – 20 to  SIRT1 transcription factor deacetylation

Normal cancer prevention and aging prevention

SIRT1 – cancer prevention via 5 ways:  (+) cancer-specific apoptosis by deacetylating survivin, (-) cancer growth by deacetylating β-catenin, (-) cancer angiogenesis by deacetylating Notch, (+) genomic stability via deacetylating histones and NBS1,

SIRT1 –  (-) ROS damage to DNA via deacetylation leading to  Nrf2 and FOXO3, ARE expression

SIRT1 –  stress resistance by deacetylating p53, FOXO, Ku70 transcription factors, less apoptosis of healthy cells, stress resistance (this is lost with aging)

Consequence of age-induced loss of SIRT1 activity: acetylated p53 induces apoptosis (nonacetylated p53 inhibits apoptosis)

c. Mitochondrial Effects of Sirtuin Decline:  mitochondrial biogenesis,  fatty acid oxidation, mito respiration, acetate usage, and amino acid usage

Normal mitochondrial effects increasing metabolism & energy production:

SIRT1: PGC-1α deacetylation, mitochondrial biogenesis, fatty acid oxidation and respiration

SIRT3  Complex I synthesis; respiration;  Ace-CS2  acetate usage;  GDH amino acid usage

SIRT4   GDH amino acid usage

SIRT5  CPS1 amino acid usage

4. Decline in AMP Energy Sensor Activity (AMP Kinase)

a. Cytoplasmic Effects of AMPK Decline:  less active AMPK

5. Increase in mTOR kinase Activity

6. Decline in Mitochondrial Biogenesis

7. Decline in Autophagy (-) autophagy or failure of autophagy to work adequately

– mTOR overactivation,

– AMPK inhibition

– inability of SIRT1 to induce autophagy with starvation

8. Antagonistic Pleiotropy Pathways – Over- activation pathways that promote growth when you are young and aging when you are old:

a. Insulin/IGF-1/PI3K/Akt/FOXO

b. mTOR/S6k

c. Protein kinase A

d. Protein kinase B

e. Protein kinase C

f.  c-Myc

g. Ras/Raf/MEK/ERK

h. Ras/PI3K/PTEN/Akt/mTOR

9. Inflammatory pathway up regulation

           a. Inflammation due to PPAR inhibitionChronic inhibition of PPARα,γ elements (PPREs) => stimulation of inflammation via NF-kB, AP-1, STAT, an NFAT pathways

b. Inflammation due to IL-6Chronic IL-6 induced activation of inflammation, creating a precancerous microenvironment – NF-kB, Jun/Ap-1, NFAT, STAT3, & COX2 pathways

c. Inflammation due to other cytokinesChronic production of pro-inflammatory mediators due to #2          – pro-inflammatory cytokines (TNF-α, IL-1β, IL-6, IL-8, etc.)

d. Inflammation due to ROS/RNS

e. Inflammation due to senescent cells and the SASP

10. Growth factor overstimulation – growth factors and intracellular pathways involved with proliferation and growth

– EGF, VEGF, HGF, β-catenin, ERK, MAPK, JNK, etc.

11. SASP induced EMT – Precancerous cell transformation to cancer cells by the inducing the epithelial-to-mesenchymal transition (EMT) due to secretions by senescent cells (SASP)

12. Telomere uncapping – Telomere shortening and the resulting genome instability produced by uncapped telomeres

13. Telomerase activation or ALT activation – Activation of telomerase or the ALT pathway in the cancer cells to prevent p53 and p16 induced cell cycle arrest

14. Loss of Contact inhibition – Loss of cell-to-cell contact inhibition, which allows cells to continue to proliferate, despite crowding

15. ECM degradation – increased production of extracellular matrix metalloproteinases (MMPs) that make it possible for tumor cells to invade surrounding tissue

16. Loss of cell cycle control – Loss of cell cycle regulation/control by mutations or epigenetic silencing of cell cycle checkpoints

17. Cytokine-mediated tumor invasion/metastisis – up regulation of specific cytokines or cytokine receptors involved with tumor invasion and metastisis – IL-13, IL-13Rα2

18. Angiogenesis – Activation of angiogenesis by angiogenic growth factors and receptors – VEGF, HGF, TGF-α, TGF-β , PDGF, TNF-α, interleukins, chemokines, and FGF family

19. Hormonal receptor activation – Stimulation of androgen/estrogen receptors by endogenous hormones/metabolites – Androgen receptor (AR), estrogen receptor (ER), etc.

20. DNA repair defects – DNA repair mechanism defects due to mutations or non-mutational epigenetic silencing – BRCA

21. Mitochondrial mutations – Mitochondrial mutations and high ROS production, leading to increased DNA mutation rates

22. Loss of mitochondrial ATP production – loss ability to generate energy from fatty acid oxidation, leading to the cancer cell’s dependence on glucose for ATP production

23. Warburg effect – The induction of aerobic glycolysis (the Warburg effect) where cells are dependent on glucose, have high LDH levels, and this effect promotes metastisis

24. ROS resistance in cancer cells – Expression and up regulation of pathways that protect cancer cells against ROS-induced apoptosis

– Nrf2 pathway/ARE genes,  FOXO pathway, etc.

25. Apoptosis resistance – Inhibition of apoptotic factors or overexpression of anti-apoptotic factors –

26. Immune evasion – Defects in anti-tumor immune surveillance – cTGF-β, Toll-like receptors (TLRs), immune cell inhibition (NK, TIL, T, B cells), tumor-derived microvesicles, etc.

27. Cancer stem cells – The existence and selective survival of cancer stem cells in response to chemotherapy and radiation therapy, due to their resistance to apoptosis

 28. ARE/FOXO down regulation – Down regulation of anti-oxidant response elements (Nrf1/Keap1 pathway) and FOXO genes for synthesis of endogenous anti-oxidant enzymes

29 Protein aggregate accumulation – Accumulation of protein aggregates due to defects in autophagy, the UPS, improper cleavage of proteins (APP), excessive protein damage by ROS, RNS, “gain of function” mutations, or “loss of function” mutations, and epigenetic dysregulation of genes involved with protein homeostasis

30. Mitochondrial mutations – increasing presence of defective mitochondria damaged by increased levels of ROS => accelerated decline in mitochondria

31. Inadequate Mitophagy – clearance of damaged mitochondria by the mitochondrial-specific form of macroautophagy => further accumulation of defective mitochondria

32. Stem cell decline/dysfunction – Defects in stem cell function, decline in stem cell number, and the suppression of stem cell growth by microenvironment factors (SASP)

33. Cellular senescence – the accumulation of senescent cells, which is a cell that has undergone “cell cycle arrest” but will not die (i.e. “apoptosis resistance”). These cells        produce a plethora of harmful cytokines that produce chronic inflammation and stimulate the epithelial-to-mesenchymal transition (EMT), which is required for the transformation of precancerous cells to malignant cells.

34. DNA repair decline – Defective DNA repair mechanisms or declines in the efficiency and accuracy of DNA repair.


Developing a 3 Tiered Approach for Chemoprevention of Aging and Cancer – The concept of a  “Cancer Chemoprevention Pyramid” (CCP)


The pyramid illustrates the timing idea, where the foundation must be always built first.  The pyramid also illustrates the magnitude and importance of the base 1st tier, being larger and more important than the middle 2nd tier.  The upper 3rd tier likewise is smaller and less important than the second tier.  No place is this more important than in cancer prevention, where lifestyle factors have clearly been shown to affect cancer incidence and aging.

The 1st tier strategies are also simple and easy for most people to comply with.  The 2nd tier are more difficult to comply with and require much more discipline (for CR and GR), and also require the oral injestion of concentrated extracts obtained from plants and fish.  Still, very few negative side effects will occur with both 1st and 2nd tier interventions except for the negative psychological aspects of CR.  The 3rd tier of the cancer chemoprevention pyramid is the most controversial, since at this time there are no drugs FDA approved for the prevention of cancer (except for aromatase inhibitors and 5α-reductase inhibitors).  Since the FDA does not recognize aging as a disease, no drugs are approved for this indication either.  Still, there are over a dozen FDA-approved drugs that have been shown to have an anti-cancer and/or an anti-aging effect.  Most of these are well tolerated with few side effects.  Many are generic and are inexpensive as well.

The 1st Layer of a Cancer Chemoprevention PyramidThe “Big 5 Foundation” – eliminating smoking, obesity, and a high fat diet, exercising, and eating a diet rich in fruits, vegetables

.The most scientifically proven way to reduce this risk in both males and females is to stop smoking, which lowers a person’s risk by 8-12%.  The next most effective methods to reduce cancer risk is to eliminate obesity, high fat intake, exercise, and eat a diet that is rich in fruits and vegetables.  Lifestyle modifications are the “foundation of cancer prevention” and must be implemented or the additional chemoprevention strategies mentioned below will be inadequate to counter the carcinogenic effects of these “big 5” lifestyle factors.  With a  “Big 5 Foundation” chemoprevention program in place, we believe that a pyramid of additional chemopreventative measures could be implemented that would statistically reduce a person’s lifetime risk of cancer by an additional 30%.  There are possible ways of increasing the efficacy of lifestyle modification with the following additional recommendations:

1.   Specific “exercise prescription” with specific types of exercise and “doses” – This would include weight lifting with specific goals, aerobic exercise with goals of training within a specified heart rate (i.e. training heart rate), and also adding stretching exercises including yoga.  These goals would be gradually increased with time to increase the hormetic dose.  This would include heavier weights for weight lifting and more vigorous exercise, based on heart rate during exercise and heart rate recovery after exercise.

2.   Specific weight goals based on body fat and lean body mass.  For example, this would include a goal of reaching a certain body fat percentage (10-12% for males, 15-20% for females) and certain lean body mass (i.e. building up an adequate muscle mass and maintaining this).  The same idea of gradually  increasing goals would be instituted here.

3.   Specific “superfoods” to be included, such as extra virgin olive oil, red wine, green tea, green coffee beans, curry, soy products, cold water fish, flaxseeds, and lots of fresh berries, fresh vegetables, garlic, onions, and spices (turmeric, cinnamon, allspice).  Specific “dose ranges” of these foods with recipes would be encouraged, where a recipe book gave the adequate dosage.

4.   Elimination of the Western diet of high fat, red meat, fried food, high calorie foods, sugar-enriched foods, etc.

The 2nd Layer of the PyramidAlternate day fasting, calorie or carbohydrate restriction (20g/day), and chemoprevention with phytochemical xenohormetic extracts

The scientific evidence for the beneficial effects of caloric restriction (CR) is now so strong that in 2013, three randomized clinical trials have been approved using this strategy for actually treating cancer (CR for breast cancer treatment, Thomas Jefferson University; CR for prostate cancer treatment, Duke University; CR for pancreatic and lung cancer treatment, U of Iowa). Although it is unpopular, CR has scientifically been shown to reduce cancer risk and increase longevity in all model animal studies.  It is time to seriously consider adding a cocktail of natural ingredients extracted from plants to our daily intake, either as an additive to food or drinks, or in a “polypill” form, where 30-50 of the most beneficial herbal products could be combined. One “polypill” could improve the low compliance problem that has been well documented when patients have to swallow dozens of pills per day.  The list below includes herbs with a strong anticancer effect.  I believe that instituting the 1st layer of the Pyramid and the 2nd layer of the Pyramid could confer a 50% reduction in cancer risk.

Supplement Source – Name   Particular supplement Xenohormetic Ingredient Positives and Problems with the   particular Supplement
Extra virgin olive secoiridoids decarboxymethyl oleuropein aglycon Most of the secoiridoids are lost in the waste   water from the olive oil presses. It doesn’t get on the shelf
Turmeric               curcumin Best anticancer compound, but there is very low   absorption of curcumin and even lower bioavailability
Red wine and red grapes resveratrol Resveratrol is well absorbed and very   bioavailable, but is rapidly excreted by the kidneys in a few hrs
White wine and green grapes n-tyrosol, hydroxytyrosol White wine is great, but to get enough n-tyrosol   and hydroxyl tyrosol, you would have to drink all day
Cruciferous vegetables        isothiocyanates (Ex: sulforaphane)        You need to eat a bushel of broccoli, brussel   sprounts, cabbage and cauliflower every day 
Garlic allyl mercaptan, allicin Garlic smells.    Garlic extracts that do not smell do not have high levels of the   active ingredient
Onions    quercetin, rutin Onions smell and make you cry.  Extracts that do not make you tear do not   have the good ingredients
Soybeans, Kudzu genistein, soyasaponins       Soybeans are very good for many reasons.  Unfortunately, genistein also serves as a   phytoestrogen
Green tea, white tea EGCG, EGC Estimates are that you need to drink 15 glasses of   green tea per day, to get the proper dose.    May be   one of the reasons for low cancer risk in Japanese
Green coffee beans caffeic   acid and chlorogenic acid Green   coffee beans are good.  These   polyphenols are damaged by the heat with coffee bean roasting
Fish oil, Krill oil EPA, DHA There are multiple cardiovascular disease   reducable by fish or krill oil
Allspice   ericifolin                 This spice is one of the best HDAC inhibitors
Mushrooms angiogenesis   inhibitors Mushrooms   are great angiogenesis inhibitors
Cashew   nut shell oil anacardic   acid Cashew   nut shell oil is cheap and is one of the best natural HAT inhibitors and HDAC   inhibitors
Chocolate              theobromines Chocolate   actually has 3 mTOR inhibitors.    Unfortunately, chocolate candy has too much sugar
Vitamin   D3            1,125   dihyroxyvitamin D      Vitamin   D3 has been misrepresented as a vitamin.    It is actually a hormone and is good for you
Vitamin E α-tocopherol          Only the   alpha-tocopherol type of Vitamin E is really good for you.
Folic   acid folic   acid This is   the best “methyl donor” that you can take.    It is important for keeping epigenetics normal
Calcium calcium Calcium   has great anticancer effects.  Recent   studies suggest that it should be labeled as such
Selenium selenium Selenium   is an element with many isoforms that are beneficial and some that are not
Frankincense        boswellic   acid  Boswellic   acid is only found in minute quantities in plants. Our use of this as a   supplement can increase the dose
Ginger                   zerumbone Ginger is   another very good spice.  It is a good   HDAC inhibitor.  May be one of the   reasons for low cancer risk in Japanese
Bitter   melon extract charantin,   mormordin Bitter   melon extract has some unique compounds that induce apoptosis in cancer cells 
Cinnamon cinnamic   acid, hydroxycinnamic acid Cinnamon   extracts have all sorts of great features:    They are secreted by exosome release.
Cinnamon hydroxycinnamic   acid (-) HDACs
Cinnamon procyanidin   oligomers (-)   angiogenesis via VEGR-2
Mangosteen   fruit rind           prenylated   xanthones and garcinol Mangostein   rinds are one of the best HDAC inhibitors 
Grapefruit,   other sources naringenin This is   the ingredient that makes grapefruit bitter. 
Citrus   fruits, other sources   Gentisic   acid         This is   another very good ingredient in citrus fruits with multiple mechanisms of   action 
Red   apples, onion quercetin Skins of   red apples an excellent source.  Very   good mitochondrial biogenesis polyphenol 
Piper Longum extract          piperlongumine     This is a   polyphenol that increases ROS selectively in cancer cells. It should be   exploited for this
Tomatoes lycopene,   luteolin, lutein       These   polyphenols are mainly in the tomato skins, which is discarded making   tomato  juice, soup, and ketchup
Venus   flytrap extract plumbagin  
Red   sandalwood oil pterostilbene, α-santalol  
Flaxseed, chia seed linolinic, linoleic acids  
Hot chili peppers   capsaicin  
Rosemary, oregano, sage, thyme      rosemarinic acid  
Volatile oil of Radix sinensis n-butylidenephthalide    
Triphala   churna     chebulinnic   acid   
Skins   from apples, etc.                      ursolic   acid This is   one of the best polyphenol   for   addressing skin cancers; it induces apoptosis in such cells
Yerba   mate caffeine,   theobromine, theophylline Yerba   mate is a good source of all three of these polyphenols

The 3rd Layer of the Pyramid –Drug Chemoprevention (NSAIDs, COX2 inhibitors, 5-α reductase (-), aromatase (-), SARMs, SERMs, Metformin, Rapamycin, statins, H2-blockers)

 There is now a large body of evidence that several over-the-counter medications as well as several classes of prescription drugs can further reduce cancer risk. This includes aspirin, which is the acetylated form of the natural compound, salicylate.  Aspirin was once thought to only have an antipyrogen/anti-inflammatory effect via the inhibition of arachidonic acid pathways.  We now we know that there are many molecular targets for aspirin, including COX, LOX, AMPK, and mTOR.  The use of a FDA- approved drug for a new indication (anti-aging and cancer prevention) is called “drug repurposing”.  Here is a list of drugs that could be “repurposed” for cancer chemoprevention and anti-aging.  When combined with a lifestyle modification program and a botanical extract “polypill”, I suspect that adding a “polypill” of FDA approved drugs to the plan will result in a 80% reduction in cancer risk.

Drug (or Drug Category)                       FDA approved indication             Anti-aging & Anti-cancer “Drug Repurposing: mechansims of Action


NSAIDs                                       anti-inflammatory                        (-)Arachidonic cascade, (-)COX, (-) LOX, (+)AMPK, (-)mTOR

Celecoxib                                    arthritis                                         (-) COX3

Metformin                                    diabetes                                       (+)AMPK, (-) mTOR, (+) autophagy,

Rapamycin                                  organ transplant rejection drug    (-) mTOR

H2 blockers                                 acid reflux, ulcers                        (-)angiogenesis, (+) immune stimulation against cancer cells

Statins                                          hypercholesterolemia                  (-) HMG CoA

5α-reductase inhibitors                alopecia, BPH                             androgen-sensitive prostate cancer prevention

aromatase inhibitors                    breast cancer                              breast cancer prevention

orinostat (SAHA)                                                                              (-) HDACs

valproic acid                                                                                     (-) HATs

JQ1                                                male contraceptive                      (-) BET bromodomain protein 4 (BRD4)

Benzodiazepines                         anxiety, sleep                              (-) BET bromodomain protein 4 (BRD4)

Lanperisone                                 muscle relaxant                           selective ROS inducer in cancer cells

Chlorpheniramine maleate        allergy drug                                  (-) HDACs

There are some other non-FDA approved compounds that also have a great potential for reducing cancer.  Some are considered drugs. Others are considered supplements. Some are non classified of yet. They include the following:

Compound                                   Category of compound               Anti-aging and Anti-cancer mechanism of action

Melatonin                                     pineal gland hormone                  mitochondrial-specific anti-oxidant

Oxaloacetate                               Citric acid cycle intermediate      activates translocation of FOXO to the nucleus






PPAR agonists


DFMO (diflouromethylornithine)

C60 fullerenes



Integrating all 3 Tiers of the Prevention Pyramid

Molecular Solution Strategy for   an anti-anti-cancer and anti-aging effect:               Lifestyle 1st Tier of Prevention   Pyramid 2nd Tier of Prevention   Pyramid 3rd Tier of Prevention   Pyramid
Lifestyle, Food, & Beverage   Strategies Most Effective Natural Product   Strategy Drug Chemoprevention Strategies
1. HDAC inhibition caloric   restriction (CR), fasting, glucose restriction (GR), green tea, soy products,   broccoli, green coffee beans, olive oil, wine, water cress, curry, cinnamon,   ginger EGCG,   Genistein, Phenethyl isothiocyanate,     curcumin, sulforaphane, reseveratrol, I3C, hydroxycinnamic acid,   plumbagin, selenium. Trapoxin A, zerumbone SAHA,   Chlorpheniramine maleate
2. DNMT   inhibition CR,   fasting, GR, green tea, white tea, apples, grapefruits, brazil nuts, garlic,   raw or rewed tomatoes w/skins, green coffee beans EGCG,   genistein, garcinol, garlic & onion organosulfur compounds, lycopene,   lutein, luteolin, chlorogenic acid, caffeic acid
3. HAT   inhibition CR, GR,   fasting, green tea, white tea, curry, soy products Anacardic   acid, EGCG, genistein, curcumin
4. HMT   inhibition No known   1st tier interventions for this S-adenosylmethionine   (SAM) BRD4770
5.   Insulin/IGF-1 pathway inhibition CR, GR,   fasting, NO hGH tx, No Insulin tx Botanical   Klotho activators, EVOO secoiridoids 2-dexoyglucose,   metformin
6. mTOR pathway inhibition caloric   restriction, fasting caffeic   acid, EGCG, EVOO secoiridoids, quercetin rapamycin,   metformin, aspirin, sulindac, PI3K inhibitors, Akt inhibitors, MEK   inhibitors
7. AMPK   activation exercise,   CR, GR, fasting, EVOO resveratrol,   phenethyl isothiocyanate, secoiridoids, oxaloacetate metformin,   aspirin, rosiglitazone
8.   Sirtuin activation exercise,   CR, fasting, red wine, EVOO wine, EVOO resveratrol,   myricetin
9. FOXO   activation CR,   fasting, white wine, EVOO oxaloacetate,   leucine supplementation, n-Tyrosol, Hydroxytyrosol
10. Nrf2   activation exercise,   CR, fasting isothiocyanates metformin
11.   Ras/Raf pathway inhibition CR,   fasting No known   natural inhibitors of this pathway B-raf   inhibitors – aminoisoquinolone, MEK inhbitors
12. PPARα   and PPARγ activation exercise,   CR, fasting oleoylethanolamide,   phytannic acid, PQQ fibrate,   fenofibrate, ciglitazone, rosiglitazone
13. NF-kB   inhibition exercise,   CR, GR, fasting, curry, green tea, green coffee beans, Venus fly trap extract polyphenols   (curcumin, EGCG, isothiocyanates, caffeic acid, chlorogenic acid, etc.),   plumbagin
14. AP-1   inhibition or activation exercise,   CR, GR, fasting, curry, green tea, white tea, broccoli, brussel sprouts,   cabbage, watercress polyphenols   (curcumin, EGCG, isothiocyanates, etc.), plumbagin
15. JAK   and STAT3 pathway inhibition exercise,   CR, GR, fasting, wine curcumin,   resveratrol, cucurbitacin derivatives, flavopiridol, deoxytetrangomycin,   piceatannol,indirubin,plumbagin
16.   Arachidonic acid/COX2 pathway (-) No   lifestyle interventions for this Fish oil,   Krill oil, myriad algae, curcumin NSAIDs,   COX2 inhibitors
17. Heat   shock protein activation repeated   mild heat stress (RMHS), repeated mild hypoxic stress secoiridoids
18.   Retinoic acid receptor activation No   lifestyle interventions for this naturally   occuring retinoids all-trans   retinoic acid, 13-cis retinoic acid, bexarotene, fenritinide,
19.   β-catenin signaling inhibition No   lifestyle interventions for this fisetin JQ1, iBET   151, triazolo-benzodiazepine
20. c-Myc   inhibition No   lifestyle interventions for this no   naturally occuring c-Myc inhibitors
21.   VEGF/VEGFR inhibition No   lifestyle interventions for this Vit E,   fish oil, H2-blockers, mushrooms, curcumin, garlic, emodin, coleon A lactone,   gentisic acid, rapamycin many   drugs for angiogenesis inhibition
22.   EGF/EGFR inhibition No   lifestyle interventions for this
23. SKP2   inhibition (part of UPS that degrades tumor suppressor proteins) caloric   restriction, fasting gallic   acid, EGCG, quercetin, curcumin, lycopene, secoiridoids no drugs   for Skp2 inhibition
24.   Statins Lovastatin,   others
25.   Warburg effect inhibition (LDHA gene) No   lifestyle interventions for this secoiridoid   polyphenols metabolic   disruptors – 2-Deoxyglucose, MitoQ,
26.   Inhibition of cellular senescence No   lifestyle interventions for this secoiridoid   polyphenols
27.   Inducing ROS or increasing ROS       induced   apoptosis hypoxia   can augment chemotherapy-induced apoptosis;    heat can augment chemotherapy-induced apoptosis

Wrapping it up There are a great many similarities in the epigenetics and biological processes of cancer and aging.

  • Therefore, it appears that if effective means could be found to prevent cancer, those means would most likely also be preventative of aging itself.
  • The impact of widespread adoption of such means could have significant impacts on extending average human lifespans, both because of less deaths by cancer and because of the reduced rates of aging.
  • So, we have been concerned here with how common strategies might be found that address both cancer and aging.
  • A key concept to bring to bear on this issue is the process of Xenohormesis,whereby stress-response phytochemicals developed over millions of years of evolution in plants keep plants cancer-free and healthy appear to be capable of doing the same in humans.
  • We have herein provided first-level molecular explanations for the “causality” of cancer and aging.  We have described the processes in cancer and aging of epigenetic silencing of “good” genes and epigenetic activation of “bad” genes.
  • Further, we describe how these unwanted epigenetic effects can be reversed by judicious ingestion of plant-based phytochemicals.
  • We identify a 3 tiered “Pyramid” approach for chemoprevention of aging and cancer, the exact interventions involved in each layer of the Pyramid, and how the interventions in the three layers of the Pyramid can be integrated together. 


The tables and compilations of data in this and the other blog entries in the Two Dragons series are intended to be illustrative of the main points to be made.  They are compiled from various sources, in most cases are incomplete, and may contain occasional errors.



About Vince Giuliano

Being a follower, connoisseur, and interpreter of longevity research is my latest career, since 2007. I believe I am unique among the researchers and writers in the aging sciences community in one critical respect. That is, I personally practice the anti-aging interventions that I preach and that has kept me healthy, young, active and highly involved at my age, now approaching 91. I am as productive as I was at age 45. I don’t know of anybody else active in that community in my age bracket. In particular, I have focused on the importance of controlling chronic inflammation for healthy aging, and have written a number of articles on that subject in this blog. In 2014, I created a dietary supplement to further this objective. In 2019, two family colleagues and I started up Synergy Bilherbals a dietary supplement company that is now selling this product. In earlier reincarnations of my career. I was founding dean of a graduate school and a university professor at the State University of New York, a senior consultant working in a variety of fields at Arthur D. Little, Inc., Chief Scientist and C00 of Mirror Systems, a software company, and an international Internet consultant. I got off the ground with one of the earliest PhD's from Harvard in a field later to become known as computer science. Because there was no academic field of computer science at the time, to get through I had to qualify myself in hard sciences, so my studies focused heavily on quantum physics. In various ways I contributed to the Computer Revolution starting in the 1950s and the Internet Revolution starting in the late 1980s. I am now engaged in doing the same for The Longevity Revolution. I have published something like 200 books and papers as well as over 430 substantive.entries in this blog, and have enjoyed various periods of notoriety. If you do a Google search on Vincent E. Giuliano, most if not all of the entries on the first few pages that come up will be ones relating to me. I have a general writings site at and an extensive site of my art at Please note that I have recently changed my mailbox to
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