Showing posts with label tumor cells. Show all posts
Showing posts with label tumor cells. Show all posts

Shock findings in new GMO study: Rats fed lifetime of GM corn grow horrifying tumors, 70% of females die early

(NaturalNews) Eating genetically modified corn (GM corn) and consuming trace levels of Monsanto's Roundup chemical fertilizer caused rats to develop horrifying tumors, widespread organ damage, and premature death. That's the conclusion of a shocking new study that looked at the long-term effects of consuming Monsanto's genetically modified corn.

The study has been deemed "the most thorough research ever published into the health effects of GM food crops and the herbicide Roundup on rats." News of the horrifying findings is spreading like wildfire across the internet, with even the mainstream media seemingly in shock over the photos of rats with multiple grotesque tumors... tumors so large the rats even had difficulty breathing in some cases. GMOs may be the new thalidomide.
"Monsanto Roundup weedkiller and GM maize implicated in 'shocking' new cancer study" wrote The Grocery, a popular UK publication. (http://www.thegrocer.co.uk/topics/technology-and-supply-chain/monsant...)

It reported, "Scientists found that rats exposed to even the smallest amounts, developed mammary tumors and severe liver and kidney damage as early as four months in males, and seven months for females."

The Daily Mail reported, "Fresh row over GM foods as French study claims rats fed the controversial crops suffered tumors." (http://www.dailymail.co.uk/sciencetech/article-2205509/Fresh-fears-GM...)

It goes on to say: "The animals on the GM diet suffered mammary tumors, as well as severe liver and kidney damage. The researchers said 50 percent of males and 70 percent of females died prematurely, compared with only 30 percent and 20 percent in the control group."

The study, led by Gilles-Eric Seralini of the University of Caen, was the first ever study to examine the long-term (lifetime) effects of eating GMOs. You may find yourself thinking it is absolutely astonishing that no such studies were ever conducted before GM corn was approved for widespread use by the USDA and FDA, but such is the power of corporate lobbying and corporate greed.

The study was published in The Food & Chemical Toxicology Journal and was just presented at a news conference in London.

Findings from the study

Here are some of the shocking findings from the study:

• Up to 50% of males and 70% of females suffered premature death.

• Rats that drank trace amounts of Roundup (at levels legally allowed in the water supply) had a 200% to 300% increase in large tumors.

• Rats fed GM corn and traces of Roundup suffered severe organ damage including liver damage and kidney damage.

• The study fed these rats NK603, the Monsanto variety of GM corn that's grown across North America and widely fed to animals and humans. This is the same corn that's in your corn-based breakfast cereal, corn tortillas and corn snack chips.

The Daily Mail is reporting on some of the reaction to the findings:

France's Jose Bove, vice-chairman of the European Parliament's commission for agriculture and known as a fierce opponent of GM, called for an immediate suspension of all EU cultivation and import authorisations of GM crops. 'This study finally shows we are right and that it is urgent to quickly review all GMO evaluation processes,' he said in a statement. 'National and European food security agencies must carry out new studies financed by public funding to guarantee healthy food for European consumers.' (http://www.dailymail.co.uk/sciencetech/article-2205509/Fresh-fears-GM...)

Read the study abstract

The study is entitled, "A Comparison of the Effects of Three GM Corn Varieties on Mammalian Health." Read the abstract here:
http://www.biolsci.org/v05p0706.htm

That abstract include this text. Note: "hepatorenal toxicity" means toxic to the liver.

Our analysis clearly reveals for the 3 GMOs new side effects linked with GM maize consumption, which were sex- and often dose-dependent. Effects were mostly associated with the kidney and liver, the dietary detoxifying organs, although different between the 3 GMOs. Other effects were also noticed in the heart, adrenal glands, spleen and haematopoietic system. We conclude that these data highlight signs of hepatorenal toxicity, possibly due to the new pesticides specific to each GM corn. In addition, unintended direct or indirect metabolic consequences of the genetic modification cannot be excluded.

Here are some quotes from the researchers:

"This research shows an extraordinary number of tumors developing earlier and more aggressively - particularly in female animals. I am shocked by the extreme negative health impacts." - Dr Michael Antoniou, molecular biologist, King's College London.

"We can expect that the consumption of GM maize and the herbicide Roundup, impacts seriously on human health." - Dr Antoniou.

"This is the first time that a long-term animal feeding trial has examined the impact of feeding GM corn or the herbicide Roundup, or a combination of both and the results are extremely serious. In the male rats, there was liver and kidney disorders, including tumors and even more worryingly, in the female rats, there were mammary tumors at a level which is extremely concerning; up to 80 percent of the female rats had mammary tumors by the end of the trial." - Patrick Holden, Director, Sustainable Food Trust.

Spread the word: GMOs are toxic!

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Delta-24-RGD - A Virus Found to Target and Eliminate Cancer Cells of the Brain

Cancer is quite a hot topic in the scientific research community today, due to the obvious lack of knowledge underlying certain biological processes. Without the mastery of these biological pathways, it is not feasible to devise surefire treatment and/or prevention methods against specific types of cancer. One does not have to look very far to find criticism or an attempt at exploitation of these biological voids by the media. Despite the frequent scrutiny, the field of oncology (the study of tumors/cancer) has improved exponentially in understanding the manifestation, diagnosis, prevention, and treatment of cancer. A simple look at the declining morbidity rates of cancer patients over the last few decades should provide some comfort even to the most skeptical individuals.
Despite the frequent advances in cancer research, the findings manage to fly under the radar of mainstream media. It lies within these small findings, which are the basis of future treatments and cures. Recently, a group of researchers came one step closer to solving their life saving puzzle.
The study, conducted by researchers at the UT-Houston M.D. Anderson Cancer Center and funded by the National Cancer Institute, analyzed the destructive effects on brain tumor stem cells of mice by introducing a tailored adenovirus (Delta-24-RDG). By tailored adenovirus, I mean a specific virus produced by scientists. This was tested on the most aggressive brain tumor, glioblastoma multiforme, which is known to be resistant to chemotherapy and radiation. The particular intrigue in this project stems from their attempt to build on well-known and studied research performed in 2003.
The 2003 study found that Delta-24 eliminated brain tumors in 60% of mice. The recent study however, was conducted on the actual stem cells that drive the continued tumor growth postoperatively, hence the testing on glioma stem cells. This led to a direct comparison in survival time between the control group (received no intervention) and the treatment group (received Delta-24 injection). The survival time of the mice who received treatment nearly doubled that of the control group. The result is obvious: the mice that received the injection of the adenovirus demonstrated prolonged life-spans. The success of the study did not simply end there.
The researchers attempted to analyze more than mere cause and effect. They sought to gain information on the actual physiological process contributing to the death of the stem cells in the brain. For the first time, adenovirus-mediated cell death (by autophagy) was noted as the direct method of cellular death in tumor stem cells of the brain. It was also noted that the therapeutic virus did not alter normal brain tissue. This finding carries with it tremendous hope because the tumors formed in the brains of these mice closely resemble brain tumors in humans. This resemblance lies in their irregular form and invasive metastatic, or spreading, properties. The study did mention the limitations of these findings and the need for further research, but it does postulate an exciting and possible method of cancer treatment, which may not be limited to the brain. This study only hints at the remarkable and constant efforts put forth by cancer researchers. One must remember that our race for a cure is not a sprint, but an ongoing marathon that must be carefully and methodically ran.
1) Fueyo J, Alemany R, Gomez-Manzano C, Fuller GN, Khan A, Conrad CA, Liu TJ, Jiang H, Lemoine MG, Suzuki K, Sawaya R, Curiel DT, Yung WK, Lang FF. Preclinical characterization of the antiglioma activity of a tropism-enhanced adenovirus targeted to the retinoblastoma pathway. J Natl Cancer Inst. 2003 May 7;95(9):652-60. PMID: 12734316.
2) Jiang H., Gomez-Manzano C., Aoki H., Alonso M.M., Kondo S., McCormick F., Xu J., Kondo Y., Bekele B.N., Colman H., Lang F.F., Fueyo J. Examination of the therapeutic potential of Delta-24-RGD in brain tumor stem cells: role of autophagic cell death. J Natl Cancer Inst. 2007 Sep 19;99(18):1410-4. PMID: 17848677.
Eliminate Cancer Cells of the Brain