James Watson Says Antioxidants May Actually Be Causing Cancer
Celebrated geneticist James Watson, one of several researchers who won the Nobel Prize for discovering the structure of DNA, has just published what can only be called a cancer manifesto in Open Biology. It’s full of fairly harsh criticisms for current cancer researchers, but also suggests several ways forward in the “war on cancer.” Among other claims, Watson asserts that antioxidants like vitamin C — often recommended as cancer-prevention supplements — could be causing some forms of cancer. He also has harsh words for personalized medicine, and the laziness of cancer researchers.
Watson, now in his 80s, has spent a great deal of his life raising money to fund cancer research at Cold Spring Harbor Laboratory, where he’s served as director since the late 1960s. Clearly anticipating his own mortality, he mourns the lack of good leadership in cancer research:
That we now have no General of influence, much less power, say an Eisenhower or even better a Patton, leading our country’s War on Cancer says everything. Needed soon is a leader that has our cancer drug development world working every day and all through the night.
He suggests that the problem is researchers are slacking, only putting in “never frantic, largely five-day working week[s].”
He goes on to say that the current craze for “personalized medicine” that will treat cancer is just not going to work. But the main problem comes from government money being misspent:
The now much-touted genome-based personal cancer therapies may turn out to be much less important tools for future medicine than the newspapers of today lead us to hope. Sending more government cancer monies towards innovative, anti-metastatic drug development to appropriate high-quality academic institutions would better use National Cancer Institute’s (NCI) monies than the large sums spent now testing drugs for which we have little hope of true breakthroughs. The biggest obstacle today to moving forward effectively towards a true war against cancer may, in fact, come from the inherently conservative nature of today’s cancer research establishments.
He goes on to say that conventional thinking about cancer is all wrong. Antioxidants may be undermining cancer therapies and even causing cancer:
In light of the recent data strongly hinting that much of late-stage cancer’s untreatability may arise from its possession of too many antioxidants, the time has come to seriously ask whether antioxidant use much more likely causes than prevents cancer.
All in all, the by now vast number of nutritional intervention trials using the antioxidants β-carotene, vitamin A, vitamin C, vitamin E and selenium have shown no obvious effectiveness in preventing gastrointestinal cancer nor in lengthening mortality. In fact, they seem to slightly shorten the lives of those who take them. Future data may, in fact, show that antioxidant use, particularly that of vitamin E, leads to a small number of cancers that would not have come into existence but for antioxidant supplementation. Blueberries best be eaten because they taste good, not because their consumption will lead to less cancer.
It is thought that antioxidants can prevent damage to DNA from oxygen radicals. But, argues Watson, we want oxygen radicals in cancer cells because this can cause the cells to die. Taking antioxidants might be preventing cancer drugs from destroying cancer cells. Instead, he recommends patients combine anti-antioxidants with cancer drugs.
Watson also recommends an area of research, into a class of proteins called RNAi, which can be used to shut down the activity of genes. He claims that we need less than a billion dollars to win the war on cancer if we focus on RNAi research:
The total sum of money required for RNAi methodologies to reveal the remaining major molecular targets for future anti-cancer drug development need not be more than 500–1000 million dollars. Unfortunately, the NCI now is unlikely to take on still one more big science project when it is so hard-pressed to fund currently funded cancer programmes … Further financial backing, allowing many more cancer-focused academic institutions to also go big using RNAi-based target discovery as well as to let them go on to the early stages of subsequent drug discovery, is not beyond the might of the world’s major government research funding bodies nor that of our world’s many, many super billionaires. The main factor holding us back from overcoming most of metastatic cancer over the next decade may soon no longer be lack of knowledge but our world’s increasing failure to intelligently direct its ‘monetary might’ towards more human-society-benefiting directions.
Watson also wants researchers to focus on a protein called Myc, which is believed to regulate the activity of 15% of our genes. Its activity is also linked to many kinds of cancer. Using RNAi methods, it’s possible we could figure out a way to control Myc, and thus shut down pathways to cancer.
Further Reading:
Watson’s manifesto, “Oxidants, antioxidants, and the current incurability of metastatic cancers,” in Open Biology
Reuters’ Sharon Begley has a good report on what other cancer researchers think about Watson’s comments.
As seen on http://io9.com



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Jan 12, 2013 @ 16:46:00
http://www.burzynskiclinic.com/ What about him?
Mar 23, 2013 @ 01:40:42
I WAS GOING TO POST THIS
WATCH HIS DOCUMENTARY
Apr 23, 2013 @ 14:13:36
Good video. It makes a lot of sense.
Jan 12, 2013 @ 17:23:56
Cannabis cures cancer… everything else is a waste of time.. bottom line. Jesus H
Jan 13, 2013 @ 05:03:19
A good eating method your life, Fruits, Vegetables, Nuts, Seeds and Roots, is likely able to get rid of all the poisons we allow to perpetuate in our environment through the air, water supply, but that would be the nature-made foods, not chemically sprayed pesticides and chemical fertilizers to replenish nutrient depleted soil. So, unless you eat real food from nature, it looks like Cannabis oil ingestion is the GO-TO solution for every damn thing. Along with cancer, hemp has dozens of other uses. People used to grow hemp everywhere in the USA in 1700-1800s. Big money shut our sustainability down by making it illegal.
Jan 13, 2013 @ 05:24:32
Dead Rite Kris ……..Spot On Dave …but Not everything else is a waste of time mate ….except Poor Namik …but He's On His Journey haha …
Dupont And The Head of The FBI at the Time … Knocked Pot On the Head made it Illegal ….buggers … but any way all went along with it all here we are today People wont Stand Back much Longer We Need to Legalize Hemp Production as An Awesome natural Resource for All of it's Uses …..
Oh not only the Oil but Eating Fresh Bud In Food Preparations is also Very very Beneficial for Human Ailments …
emancipate 2 emanate Love M8
Jan 13, 2013 @ 07:10:14
blah blah blah – I can see you are an "expert" on nutritional science. I DID NOT dispute any N'health claims for the canabis, DON'T read WHAT'S NOT WRITTEN dude !
Apr 23, 2013 @ 20:35:45
^^Don't you hate it when people put words into your mouth?
Jan 13, 2013 @ 02:22:05
Ha, ha, haa – in regards to VITAMIN C, Dr Watson is deadly wrong; there are HUNDREDS OF medical references which contradict his opinion. He shoud read the greatest scientist of the 20th century: LYNUS PAULING!
Jan 13, 2013 @ 02:25:17
doubt it ^ why would we need to take supplements at all you crazy person.. they are man made concoctions that manitulate your tissues at a cellular level, ofcourse over time cancrs are going to show up.. it is common sense is the cll is being manipulated by and outside source, eventually itll take on the inherent issues that come with the ingredients of such pills
Jan 13, 2013 @ 03:04:45
That is nonsense; you don't understand this: all those supplements are normaly present in healthy young people, but are diminished when the body gets older. So, taking supplements is a part of healthy nutrition. Read something good…!!!
Jan 13, 2013 @ 03:21:31
man your points are so vague it is ridiculous, tell me what exactly these supplements do smartas. Cannabis is all we need ON top of a natural diet
Jan 13, 2013 @ 03:35:19
David Canavan – ha, haa, you want a free course from me ! Of course it seems to you VAGUE because of all that canabis…IF YOU ARE NOT A HEMOROID, GET OF MY ARSE
Jan 13, 2013 @ 14:21:00
Im a University student and a hockey coach as well as a Cannabis user. You want a lesson from Mr. Closed Minded. Keep taking flu shots and vaccines and supplements and Ill just use common sense and eat a diet rich in the natural vitamins and minerals i need daily.. Goodluck Namik, you still havent gotten to your point here at all.. Do you want people to keep buying bottles of pharmaceutical "vitamin" supplements orr do you have any valid point suggesting why these pills containing fillers are really needed at all.
Its funny though Dr. Napkin because for being 20 years old, I think I'm more open-minded to the thought of these "medicines" and "vitamins" and "treatments" are all really just being a vicious cycle of profits perpetrated by the very government we so welcoming have control our lives, than you will ever be. You want to make a valid point then do so , else stop supporting people BUYING this garbage – like do you really think if someone is calcium deficient they should jump right to supplements, god you're stupid and lazy man. Do like 1 google search on supplements and read up FOR YOURSELF buttlover
Jan 13, 2013 @ 14:22:37
Namik Omerspahic … supplements arent found in the healthy young person, these specific nutrients are found in the body, we continue to maintain these level through diet. You are just an ignorant fuck .
Jan 13, 2013 @ 14:27:50
Chemo therapy stops the division of cells in hopes that all the "Cancer" cells stop dividing right? Well if you stop the division of cells then introduce a drug that shuts off the genes of cells (Which wouldn't be quarantined in anyone place in the body) sounds like a horrible thing. I mean aren't the "Cancerous" cells just corrupted cells who don't do their normal functions so wouldn't that create more stupid cells. Cannabis invades the cell and tells it to hurry up and die because its Rouge hence you have Apoptosis so one would think that this is the place to start research. Right or Wrong ???? And the delivery system for Cannabis is THC and CBDs which are Fats so that's why their able to enter the cells so easily. Seems like a easy start.
Mar 23, 2013 @ 02:53:24
THIS GUY IS A FREUD! He took credit for research that someone else did!
Jan 13, 2013 @ 03:09:33
Secondly, Dr Watson's main reference for not taking vit. C seriously is one study by Dr G. Bjelakovic! It was meta-analisys which took many studies which HAD VERY SMALL AMOUNT OF VIT. C, contrary to the reccommended higher dose (2,000-3000 mg per day – Pauling and others).
Jan 13, 2013 @ 03:40:23
Analee Newitz: your writing here is irresponsible since those studies you mention are biased; (VERY SMALL AMOUNT OF VIT. C USED, contrary to recommendations of Dr Pauling and others…)
Jan 13, 2013 @ 04:19:31
keep buying supplements you ignorant shitstick… support your Rothschild vionist society . god you make me sick man. You picture is of house, clearly your a sheep whom half his life is spent glued to a television . your "conditioning". Wake up.
Jan 13, 2013 @ 05:11:26
Hey Dave,
mate That's What Television Does to People ….Turns Ya Brains To Mush …..hahaha
Jan 13, 2013 @ 04:21:56
Why does the answer always have to come from some drug created in a lab that we must pay for to use?
Jan 13, 2013 @ 05:14:11
gee James, I'd be more inclined to ask your buddy Francis Crick what " he" thinks about the subject, since "he" seemed to be the one with more "insight" on the subject of DNA. http://www.cracked.com/article_16532_the-5-greatest-things-ever-accomplished-while-high.html
Jan 13, 2013 @ 05:18:00
oh and what happened to that doctor(on 20/20 new show).
growing patients cancer and testing them against the 350 known cancer drugs which many would work against different cancers than they were supposedly targeted for.
Jan 13, 2013 @ 09:27:45
food grade hydrogen peroxide which oxygenates the cells is the cure, oxidation is akin to rust and not a benificial situation either…look it up…
Feb 18, 2013 @ 02:52:56
Urgggh, he gets so much wrong in this. He is basically stating the old elitist 'Scientism' philosophy that the 'elites' of science always can be identified and merely supporting this core of researchers is all that is needed to promote scientific progress and treatments. He even describes there as being a problem resulting from a LACK of a 'war general' like leader controlling scientific investigation! Yet, that is itself deeply damaging to science and in itself unscientific. Science is not what certain appointed individuals happen to promote 'is science'. Science exists completely outside of the opinions of any individual scientist. At most, science as a process can be described as a reasonable but persistent and patient dialogue in which that dialogue is recorded and uses methods to promote reasonable interpretations and challenges unreasonable ones, and where such outcomes are dutifully incorporated as relevant in the world view by all involved in the scientific community, to inform further discourse and development in a progressive way towards a 'more scientific' future. It is CERTAINLY the case that a centralised, hierarchial system of grant control and scientific opinion DAMAGES this development, which is precisely why it has failed so much in the last 30 years, especially in the Western biological and medical sciences, notably in the area of chemotherapy, where this conventional model had clearly stopped making progress and had very limited success in developing genuine treatments. Since then, much more integrated models of cancer, and innovative treatment approaches have appeared, precisely because it has decentralised. Today most new science is coming about much more openly, indeed I can state a lot is appearing completely outside the established communities, much also by people who aren't research scientists in Watson's book. His view is outdated 'Scientism' – Science as an elitist, snobby and fundamentalist set of assumptions and facts and with vastly excessive over confidence in itself, and used lazily by certain individuals to elevate their own importance and attack and shut down debate against more earnest, and mature scientists/thinkers that they deem unworthy, often due to their style of thought or approach being unrefined, or insufficiently deferrant and unquestioning to their facts/beliefs. Simply put, this approach denigrates anyone who disagrees even with very good reason, as 'unscientific' and can affect a shut down on their careers, publication and research, which in turn locks the 'scientists' into an un-evolving mindset, which means new discoveries and novel groundbreaking research simply cannot happen. That would be fine, if the 'book of science/truth' was already 100% complete, but as it isn't, and as we have exhausted the same old strategies in using that science to solve problems, it is apparent that progress *requires a different way of thinking and funding*. I cannot stand the assumption that 'elite' Western (or other) academies or institutions produce science worth looking at and everyone else doesn't, that quite a lot of scientists believe. If anything the 'elite' few institutions are doing derivative, copy cat research and passing it off as their own. Scientists I know have said that they don't trust papers from any 'third world' institution or in any but a handful of established Journals. By implication, they make the seriously unscientific error of assuming that they should not properly question such cultures and their conclusions, or their leading spokespeople. Watson is clearly suffering a classic Scientism superiority complex. Given that he himself WAS NOT that original in his DNA work and partly passed off as his own an 'outsiders' discoveries, that of Rosalind Franklin without drawing any attention to her work and the role it had in 'his' own discoveries, he demonstrates a total and sickeningly arrogant disregard for REAL scientists, and further for the universalism of Science and scientists (who can be with or without tenure or qualifications at any institution or without), and a total lack of respect and humility, which are very bad traits in a scientist which further impair the scientific ability, which requires objectivity and commitment to real scientific principles, not elitist opinions of a self appointed, dictatorial and fascist 'scientific' priesthood purely because it believes its automatically superior, as would be by reflection, its members.
Feb 18, 2013 @ 08:10:27
Certainly, so called 'authorities' in scientific institutions misuse their reputation, giving opinion that is outside their expertise; here we have an example with Dr Watson…
Feb 18, 2013 @ 03:30:33
His attack on antioxidants like vitamin C in cancer is also based on well known scientific opinion, we certainly do not need to change back scientific culture 30+ years to realise this! Its also very misleading. Some, but definitely not all, antioxidants may increase the growth of cancer. There is little to no evidence that this increase the risk, in fact, in general many/most cancer researchers now believe that antioxidants will reduce the carcinogenic processes that cause cancer in the first place. Other antioxidants and related to which, anti-inflammatory treatments are being investigated due to clear evidence that inflammation and damage signalling can 'convert' cells into more cancerous and aggressively growing tumours. This is beyond question but it is not a simple and clear picture ie 'antioxidants are always good/ always bad'. Further, there are many research findings and publications which show many antioxidants with strong anto-tumour abilities, even against advanced and treatment resistant cancers, such that with conventional chemotherapy/radiotherapy, they amplify the effectiveness of that treatment, and do so because many natural antioxidants are protective and behave as antioxidants in healthy, metabolically normal tissue, but have THE OPPOSITE EFFECT IN TUMOR CELLS, and that protective effects in normal tissues reduce harm done / side-effects by chemo/radiotherapy, but also reduce the 'bystander effect' whereby injury and inflammation around cancer cells cause it to spread and to convert those damaged tissues to be cancerous or support cancer growth and invasion. More findings IRONICALLY SUPPORT THIS FACT WITH THE USE OF INTRAVENOUS VITAMIN C against cancer, which is prooxidant in cancer cells, BUT NOT NORMAL CELLS. The need to protect against healthy tissue damage is increasingly recognised to protect against cancer growth and spread, therefore antioxidants and other nutrients are not automatically bad. He is hugely over generalising and talking RUBBISH.
Feb 23, 2013 @ 21:39:25
Never thought I would have the experience to disagree with Watson, but his logic is ass backwards. To paraphrase, don't eat blueberries because our poisonous cancer drugs don't kill the cancer cells. OH BOY! what an ass! How about EAT blueberries and good food so you don't get cancer cells. Fumb Duck!
Feb 24, 2013 @ 00:05:50
lmao!
Feb 25, 2013 @ 15:51:17
I would state simply, that he doesn't realise that all the main points he has made in the article and in his paper, are known already to good researchers in the field, which you can easily determine by reading a broad array of papers, especially recent ones, but yet they have already taken these ideas much further and realise a more advanced concept of anti-oxidant and pro-oxidant properties and other interactions, more propperly identified as 'Redox factors'. On his point that research should where possible go after the fundamental aspect of cancers that they generally have in common, again this is widely known and occurring already due to research on ways to exploit compounds hyper-accumulated cancers including antioxidants and nutrients critical to growth (although its important to realise that immune cells needed to fight the cancer and infection also can be adversely affected as they too have similar properties and requirements so this needs intelligent work), and in fact because cancers have similarities to immune cells and share similar growth, migration and metastatic like pathways such as via cytokines and inflammation induced largely by ROS, the action of agents to control ROS and inflammation can paradoxically help combat cancer growth and transformation. So researchers already are looking at general pathways 'unique' to cancer cells, and there are many more than he highlights. Particularly, ROS interference by antioxidants is different in cancer cells and seems to act via a change in the signalling of ROS and an increase in ROS where it is harmful to the cancer cell, and generally not at all in normal cells. The action goes beyond simple antioxidant action, it may involve also vital metabolic functions, which is why antioxidants like Lipoic Acid and Acetyl L Carnitine and Ubiquinol/Ubiquinone are promising. These can act as prooxidants but also assist normal functioning, and are showing interesting potential as anticancer agents already in studies, able to shrink tumours or increase the power of other chemotherapy. D-limonene acts as an antioxidant in normal cells but hyperaccumulates in cancer cells and has anti-tumour activity, and appears to destabilise the cell. Selenium is another agent that promotes antioxidant defenses in normal cells but hyperaccumulates in cancer cells and at a relatively low multiple of a safe dose, can promote toxic effects and a pro-oxidant net action/disruption of antioxidant defenses, with well researched and strong anti-cancer effects, particularly synergism with other treatments. Lipoic acid, as an aside, may be able to greatly increase the action of vitamin C presumable emulating its proxidant action at higher doses, so that lower doses that are normal antioxidant can become prooxidant. Vitamin C is also hyper-accumulated by cancer cells. He attacks blueberries and 'superfoods' but is obviously ignorant of polyphenols, like those in olives, with very strong and promising antitumour affects. Again, these are consistent with the general finding that these agents are anti-tumor as well as assist the activity of chemotherapy or radiotherapy, and particularly in difficult to treat tumours. Its not just indicating a purely preventative effect! The phenolic group contains other candidates for anti-tumor as well as anti-mutagenic effects, and which can work well with existing treatments, and have not been well enough studied. A number of antioxidants, such as lutein, alpha-carotene also function as agents that can reverse mutated cells into healthy cells such as in the bowel, as does other antioxidants, so showing they are selective, improve the tissue environment and so combat the complex interactions known to facilitate hard to treat cancer and allow it to hide in the body, including potential use in reversing the bystander effect, which plays a key role in the generation, return of and treatability of cancer. He says don't eat blueberries (classic polyphenol rich superfood) or any antioxidant rich superfoods to fight disease, take them just *only* because they "taste good" which is complete nonsense. Then there is agents like Gamma Tocopherol, another one with antioxidant properties, that appears to *strongly* reduce the risk of cancer, and it appears to help shrink cancers. It does this by more than one means, including attacking the cytoplasm structure, IIRC, but clearly not in normal cells. High alpha-tocopherol (vitamin E) may have promoted cancer and all cause mortality simply because it blocks tissue levels of gamma-tocopherol.
Feb 25, 2013 @ 15:54:59
Moreover, his solution to the 'problem' he proposes to be more centralisation of research efforts and control over funding; all this would do is destroy diversity of research, and in all probability, it would have created an even bigger tendency which he centrally complains about, of doing fancy genetically targetted research instead of finding general factors, which many people are doing, and not at the big institutions like he describes. His prescription would impair cancer research and just make it more commercially influenced and less likely to make fundamental breakthroughs in understanding. He has a track record of snobbery and talking rot, and clearly he ignores research from 'lesser' establishments. Worst advocate around, he is.
Feb 25, 2013 @ 16:03:10
He also goes on about the need for braver researchers doing glory-type research and thinking outside the box. Yet his institutionalised model would definitely destroy that. Some of the people doing that kind of research aren't even scientists, they are medical doctors, who have found effective treatments by trial and error. In the majority of cases, these are completely ignored by centralised scientific organisations, and that is a legacy of his kind of institution.
Feb 25, 2013 @ 17:27:24
In who I would get prefer to get wisdom and guidance from, the musings of Mr. T would be preferable to James Watson. That's the state of it. And Worlds Craziest Fools is on tonight as well.
Feb 25, 2013 @ 23:26:16
Publication: 2010 Apr;31(4):687-94. doi: 10.1093/carcin/bgp332. Epub 2010 Jan 22.
Free Text: A gamma-tocopherol-rich mixture of tocopherols inhibits chemically induced lung tumorigenesis in A/J mice and xenograft tumor growth.
abstract
The present study investigated the effects of a preparation of a gamma-tocopherol-rich mixture of tocopherols (gamma-TmT) on chemically induced lung tumorigenesis in female A/J mice and the growth of H1299 human lung cancer cell xenograft tumors. In the A/J mouse model, the lung tumors were induced by either 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK; intraperitoneal injections with 100 and 75 mg/kg on Week 1 and 2, respectively) or NNK plus benzo[a]pyrene (B[a]P) (8 weekly gavages of 2 mumole each from Week 1 to 8). The NNK plus B[a]P treatment induced 21 tumors per lung on Week 19; dietary 0.3% gamma-TmT treatment during the entire experimental period significantly lowered tumor multiplicity, tumor volume and tumor burden (by 30, 50 and 55%, respectively; P < 0.05). For three groups of mice treated with NNK alone, the gamma-TmT diet was given during the initiation stage (Week 0 to 3), post-initiation stage (Week 3 to 19) or the entire experimental period, and the tumor multiplicity was reduced by 17.8, 19.7 or 29.3%, respectively (P < 0.05). gamma-TmT treatment during the tumor initiation stage or throughout the entire period of the experiment also significantly reduced tumor burden (by 36 or 43%, respectively). In the xenograft tumor model of human lung cancer H1299 cells in NCr-nu/nu mice, 0.3% dietary gamma-TmT treatment significantly reduced tumor volume and tumor weight by 56 and 47%, respectively (P < 0.05). In both the carcinogenesis and tumor growth models, the inhibitory action of gamma-TmT was associated with enhanced apoptosis and lowered levels of 8-hydroxydeoxyguanine, gamma-H2AX and nitrotyrosine in the tumors of the gamma-TmT-treated mice. In cell culture, the growth of H1299 cells was inhibited by tocopherols with their effectiveness following the order of delta-T > gamma-TmT > gamma-T, whereas alpha-T was not effective. These results demonstrate the inhibitory effect of gamma-TmT against lung tumorigenesis and the growth of xenograft tumors of human lung cancer cells. The inhibitory activity may be due mainly to the actions of delta-T and gamma-T.
A gamma-tocopherol-rich mixture of tocopherols inhibits colon inflammation and carcinogenesis in azoxymethane and dextran sulfate sodium-treated mice.
Publication: 2009 Feb;2(2):143-52. doi: 10.1158/1940-6207.CAPR-08-0099. Epub 2009 Jan 20.
Free Text: A gamma-tocopherol-rich mixture of tocopherols inhibits colon inflammation and carcinogenesis in azoxymethane and dextran sulfate sodium-treated mice.
abstract
We investigated the effects of a gamma-tocopherol-rich mixture of tocopherols (gamma-TmT, containing 57% gamma-T, 24% delta-T, and 13% alpha-T) on colon carcinogenesis in azoxymethane (AOM)/dextran sulfate sodium (DSS)-treated mice. In experiment 1, 6-week-old male CF-1 mice were given a dose of AOM (10 mg/kg body weight, i.p.), and 1 week later, 1.5% DSS in drinking water for 1 week. The mice were maintained on either a gamma-TmT (0.3%)-enriched or a standard AIN93M diet, starting 1 week before the AOM injection, until the termination of experiment. In the AOM/DSS-treated mice, dietary gamma-TmT treatment resulted in a significantly lower colon inflammation index (52% of the control) on day 7 and number of colon adenomas (9% of the control) on week 7. gamma-TmT treatment also resulted in higher apoptotic index in adenomas, lower prostaglandin E2, leukotriene B4, and nitrotyrosine levels in the colon, and lower prostaglandin E2, leukotriene B4, and 8-isoprostane levels in the plasma on week 7. Some of the decreases were observed even on day 7. In experiment 2 with AOM/DSS- treated mice sacrificed on week 21, dietary 0.17% or 0.3% gamma-TmT treatment, starting 1 week before the AOM injection, significantly inhibited adenocarcinoma and adenoma formation in the colon (to 17-33% of the control). Dietary 0.3% gamma-TmT that was initiated after DSS treatment also exhibited a similar inhibitory activity. The present study showed that gamma-TmT effectively inhibited colon carcinogenesis in AOM/DSS-treated mice, and the inhibition may be due to the apoptosis-inducing, anti-inflammatory, antioxidative, and reactive nitrogen species-trapping activities of tocopherols.
Inhibition of inflammation and carcinogenesis in the lung and colon by tocopherols.
Publication: 2010 Aug;1203:29-34. doi: 10.1111/j.1749-6632.2010.05561.x.
Free Text: Inhibition of inflammation and carcinogenesis in the lung and colon by tocopherols.
abstract
tocopherols, which exist in alpha, beta, gamma, and delta forms, are antioxidative nutrients also known as vitamin E. Although alpha-tocopherol (alpha-T) is the major form of vitamin E found in the blood and tissues, gamma- and delta-T have been suggested to have stronger anti-inflammatory activities. In the present study, using a tocopherol mixture that is rich in gamma-T (gamma-TmT, which contains 57%gamma-T), we demonstrated the Inhibition of inflammation as well as of cancer formation and growth in the lung and colon in animal models. When given in the diet at 0.3%, gamma-TmT inhibited chemically induced lung tumorigenesis in the A/J mice as well as the growth of human lung cancer cell H1299 xenograft tumors. gamma-TmT also decreased the levels of 8-hydroxydeoxyguanosine, gamma-H2AX, and nitrotyrosine in tumors. More evident anti-inflammatory and cancer preventive activities of dietary gamma-TmT were demonstrated in mice treated with azoxymethane and dextran sulfate sodium. These results demonstrate the antioxidative, anti-inflammatory, and anticarcinogenic activities of tocopherols.
Feb 25, 2013 @ 23:53:31
Chemopreventive activity of vitamin E in breast cancer: a focus on γ- and δ-tocopherol.
Publication: 2011 Nov;3(11):962-86. doi: 10.3390/nu3110962. Epub 2011 Nov 14.
abstract
vitamin E consists of eight different variants: α-, β-, γ-, and δ-tocopherols (saturated phytyl tail) and α-, β-, γ-, and δ-tocotrienols (unsaturated phytyl tail). cancer prevention studies with vitamin E have primarily utilized the variant α-tocopherol. To no avail, a majority of these studies focused on variant α-tocopherol with inconsistent results. However, γ-tocopherol, and more recently δ-tocopherol, have shown greater ability to reduce inflammation, cell proliferation, and tumor burden. Recent results have shown that γ-enriched mixed tocopherols inhibit the development of mammary hyperplasia and tumorigenesis in animal models. In this review, we discuss the possible differences between the variant forms, molecular targets, and cancer-preventive effects of tocopherols. We recommend that a γ-enriched mixture, γ- and δ-tocopherol, but not α-tocopherol, are promising agents for breast cancer prevention and warrant further investigation.
δ-tocopherol is more active than α – or γ -tocopherol in inhibiting lung tumorigenesis in vivo.
Publication: 2011 Mar;4(3):404-13. doi: 10.1158/1940-6207.CAPR-10-0130.
A gamma-tocopherol-rich mixture of tocopherols inhibits colon inflammation and carcinogenesis in azoxymethane and dextran sulfate sodium-treated mice.
Publication: 2009 Feb;2(2):143-52. doi: 10.1158/1940-6207.CAPR-08-0099. Epub 2009 Jan 20.
abstract
We investigated the effects of a gamma-tocopherol-rich mixture of tocopherols (gamma-TmT, containing 57% gamma-T, 24% delta-T, and 13% alpha-T) on colon carcinogenesis in azoxymethane (AOM)/dextran sulfate sodium (DSS)-treated mice. In experiment 1, 6-week-old male CF-1 mice were given a dose of AOM (10 mg/kg body weight, i.p.), and 1 week later, 1.5% DSS in drinking water for 1 week. The mice were maintained on either a gamma-TmT (0.3%)-enriched or a standard AIN93M diet, starting 1 week before the AOM injection, until the termination of experiment. In the AOM/DSS-treated mice, dietary gamma-TmT treatment resulted in a significantly lower colon inflammation index (52% of the control) on day 7 and number of colon adenomas (9% of the control) on week 7. gamma-TmT treatment also resulted in higher apoptotic index in adenomas, lower prostaglandin E2, leukotriene B4, and nitrotyrosine levels in the colon, and lower prostaglandin E2, leukotriene B4, and 8-isoprostane levels in the plasma on week 7. Some of the decreases were observed even on day 7. In experiment 2 with AOM/DSS- treated mice sacrificed on week 21, dietary 0.17% or 0.3% gamma-TmT treatment, starting 1 week before the AOM injection, significantly inhibited adenocarcinoma and adenoma formation in the colon (to 17-33% of the control). Dietary 0.3% gamma-TmT that was initiated after DSS treatment also exhibited a similar inhibitory activity. The present study showed that gamma-TmT effectively inhibited colon carcinogenesis in AOM/DSS-treated mice, and the inhibition may be due to the apoptosis-inducing, anti-inflammatory, antioxidative, and reactive nitrogen species-trapping activities of tocopherols.
Cancer. 2013 Jan 15;119(2):363-70. doi: 10.1002/cncr.27719. Epub 2012 Jul 3.
Phase 2 trial of daily, oral Polyphenon E in patients with asymptomatic, Rai stage 0 to II chronic lymphocytic leukemia.
Shanafelt TD, Call TG, Zent CS, Leis JF, LaPlant B, Bowen DA, Roos M, Laumann K, Ghosh AK, Lesnick C, Lee MJ, Yang CS, Jelinek DF, Erlichman C, Kay NE.
Source
Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota 55905, USA. shanafelt.tait@mayo.edu
Abstract
BACKGROUND:
The objective of the current study was to follow up the results of phase 1 testing by evaluating the clinical efficacy of the green tea extract Polyphenon E for patients with early stage chronic lymphocytic leukemia (CLL).
METHODS:
Previously untreated patients with asymptomatic, Rai stage 0 to II CLL and an absolute lymphocyte count (ALC) ≥ 10 × 10(9) /L were eligible for this phase 2 trial. Polyphenon E with a standardized dose of epigallocatechin gallate (EGCG) (2000 mg per dose) was administered twice daily.
RESULTS:
A total of 42 patients received Polyphenon E at a dose of 2000 mg twice daily for up to 6 months. Of these patients, 29 (69%) had Rai stage I to II disease. Patients received a median of 6 cycles of treatment (range, 1 cycle-6 cycles). The most common grade 3 side effects (according to National Cancer Institute Common Terminology Criteria for Adverse Events) were transaminitis (1 patient), abdominal pain (1 patient), and fatigue (1 patient). Clinical activity was observed, with 13 patients (31%) experiencing a sustained reduction of ≥ 20% in the ALC and 20 of 29 patients (69%) with palpable adenopathy experiencing at least a 50% reduction in the sum of the products of all lymph node areas. EGCG plasma levels after 1 month of therapy were found to be correlated with reductions in lymphadenopathy (correlation co-efficient, 0.44; P =.02). Overall, 29 patients (69%) fulfilled the criteria for a biologic response with either a sustained decline ≥ 20% in the ALC and/or a reduction ≥ 30% in the sum of the products of all lymph node areas at some point during the 6 months of active treatment.
CONCLUSIONS:
Daily oral EGCG in the Polyphenon E preparation was well tolerated by patients with CLL in this phase 2 trial. Durable declines in the ALC and/or lymphadenopathy were observed in the majority of patients.
Copyright © 2012 American Cancer Society.
PMID:
22760587.
[PubMed - indexed for MEDLINE].
Chemopreventive effect of aerosolized polyphenon E on lung tumorigenesis in A/J mice.
Publication: 2007 May;9(5):401-5.
abstract
effective chemoprevention of lung cancer in high-risk patients through the administration of pharmacologic or nutritional agents is urgently needed. Aerosol inhalation can deliver Chemopreventive agents directly to the respiratory tract to inhibit the tumorigenic process. In this study, polyphenon E (PolyE) and (-)-epigallocatechin-3-gallate (EGCG) were administered by aerosol delivery to A/J mice beginning 2 weeks after carcinogen treatment and continuing daily by inhalation throughout the remainder of the study (20 weeks). PolyE decreased tumor load by approximately 59%. However, EGCG, both at the same dose and at a higher dose, failed to inhibit lung carcinogenesis. These results indicate that aerosol delivery of PolyE, but not EGCG, may be a useful chemopreventive protocol in subjects at high risk for lung cancer. What was he saying about superfoods and 'antioxidants' again?
Feb 26, 2013 @ 00:02:48
Just a handful of relevant recent studies, the following show both preventative and actual anti-tumor activities.
Chemopreventive activity of vitamin E in breast cancer: a focus on γ- and δ-tocopherol.
Publication: 2011 Nov;3(11):962-86. doi: 10.3390/nu3110962. Epub 2011 Nov 14.
abstract
vitamin E consists of eight different variants: α-, β-, γ-, and δ-tocopherols (saturated phytyl tail) and α-, β-, γ-, and δ-tocotrienols (unsaturated phytyl tail). cancer prevention studies with vitamin E have primarily utilized the variant α-tocopherol. To no avail, a majority of these studies focused on variant α-tocopherol with inconsistent results. However, γ-tocopherol, and more recently δ-tocopherol, have shown greater ability to reduce inflammation, cell proliferation, and tumor burden. Recent results have shown that γ-enriched mixed tocopherols inhibit the development of mammary hyperplasia and tumorigenesis in animal models. In this review, we discuss the possible differences between the variant forms, molecular targets, and cancer-preventive effects of tocopherols. We recommend that a γ-enriched mixture, γ- and δ-tocopherol, but not α-tocopherol, are promising agents for breast cancer prevention and warrant further investigation.
δ-tocopherol is more active than α – or γ -tocopherol in inhibiting lung tumorigenesis in vivo.
Phase 2 trial of daily, oral Polyphenon E in patients with asymptomatic, Rai stage 0 to II chronic lymphocytic leukemia.
Abstract
The objective of the current study was to follow up the results of phase 1 testing by evaluating the clinical efficacy of the green tea extract Polyphenon E for patients with early stage chronic lymphocytic leukemia (CLL).
METHODS:
Previously untreated patients with asymptomatic, Rai stage 0 to II CLL and an absolute lymphocyte count (ALC) ≥ 10 × 10(9) /L were eligible for this phase 2 trial. Polyphenon E with a standardized dose of epigallocatechin gallate (EGCG) (2000 mg per dose) was administered twice daily.
RESULTS:
A total of 42 patients received Polyphenon E at a dose of 2000 mg twice daily for up to 6 months. Of these patients, 29 (69%) had Rai stage I to II disease. Patients received a median of 6 cycles of treatment (range, 1 cycle-6 cycles). The most common grade 3 side effects (according to National Cancer Institute Common Terminology Criteria for Adverse Events) were transaminitis (1 patient), abdominal pain (1 patient), and fatigue (1 patient). Clinical activity was observed, with 13 patients (31%) experiencing a sustained reduction of ≥ 20% in the ALC and 20 of 29 patients (69%) with palpable adenopathy experiencing at least a 50% reduction in the sum of the products of all lymph node areas. EGCG plasma levels after 1 month of therapy were found to be correlated with reductions in lymphadenopathy (correlation co-efficient, 0.44; P =.02). Overall, 29 patients (69%) fulfilled the criteria for a biologic response with either a sustained decline ≥ 20% in the ALC and/or a reduction ≥ 30% in the sum of the products of all lymph node areas at some point during the 6 months of active treatment.
CONCLUSIONS:
Daily oral EGCG in the Polyphenon E preparation was well tolerated by patients with CLL in this phase 2 trial. Durable declines in the ALC and/or lymphadenopathy were observed in the majority of patients.
PMID: 22760587.
Chemopreventive effect of aerosolized polyphenon E on lung tumorigenesis in A/J mice.
Publication: 2007 May;9(5):401-5.
abstract
effective chemoprevention of lung cancer in high-risk patients through the administration of pharmacologic or nutritional agents is urgently needed. Aerosol inhalation can deliver Chemopreventive agents directly to the respiratory tract to inhibit the tumorigenic process. In this study, polyphenon E (PolyE) and (-)-epigallocatechin-3-gallate (EGCG) were administered by aerosol delivery to A/J mice beginning 2 weeks after carcinogen treatment and continuing daily by inhalation throughout the remainder of the study (20 weeks). PolyE decreased tumor load by approximately 59%. However, EGCG, both at the same dose and at a higher dose, failed to inhibit lung carcinogenesis. These results indicate that aerosol delivery of PolyE, but not EGCG, may be a useful chemopreventive protocol in subjects at high risk for lung cancer.
What was he saying about superfoods and 'antioxidants' again?
Mar 21, 2013 @ 22:28:06
"Taking antioxidants might be preventing cancer drugs from destroying cancer cells."…lol. yeah, that makes sense, don't want to interfere with those awesome drugs…
Mar 22, 2013 @ 02:54:06
The ancients knew what they were doing. Fasting every season to flush the body of old cells and regeneration of new cells and herbal fomulas have been the way of mankind. Legalize our "drugs" and properly show how to use them will lead to an end to this…"how to become your own doctor" is a great read.
Mar 23, 2013 @ 05:06:03
Tell this all to Ray Kurzweil, He seems to be doing okay. And he takes 150 pills a day.
Apr 23, 2013 @ 09:52:49
What will they say next? McDonald's is the cure for cancer?
Apr 30, 2013 @ 10:06:33
& what the heck is an anti-antioxidant sounds like he is saying eat foods that creates free radicals which does not make sense because oxidation ages things it does not keep you healthy.