Guest guest Posted March 31, 2002 Report Share Posted March 31, 2002 MEDLINEplus: Serotonin Blocker May Blunt Cancer Cell " Suicide " - http://www.nlm.nih.gov/medlineplus/news/fullstory_6798.html - Serotonin Blocker May Blunt Cancer Cell " Suicide " Reuters Wednesday, March 27, 2002 LONDON, Mar 26 (Reuters Health) - Serotonin, a brain chemical that regulates mood, has the capacity to cause certain cancer cells to self-destruct, a British researcher showed on Tuesday. The findings could pave the way for new treatments for a specific type of cancer called lymphoma. The research also shows that antidepressant drugs like Prozac block the ability of serotonin to trigger tumour cell death, raising the theoretical possibility that the drugs could increase cancer risk. But Professor John Gordon of the University of Birmingham, UK, who conducted the study, said patients should keep taking their drugs since there is no evidence of any link in practice. In test-tube experiments on a type of cancer called Burkitt's lymphoma, Gordon and others found that serotonin caused cancerous cells to die off. Burkitt's lymphoma normally forms in the neck or the stomach. It affects 2% of people with AIDS and is most common in central Africa. Through a series of experiments, the British researchers clarified the mechanism by which serotonin enters lymphoma cells and triggers a mechanism called apoptosis, or programmed cell death. The research is published in the online edition of the medical journal Blood. " Because we know the mechanism, we are now in a position to develop drug analogues of serotonin that will do the same job but have better pharmacological properties, " Gordon told Reuters. The work also provides an intriguing insight into the way that " positive thinking " associated with high serotonin levels may play a key part in effective cancer care. The mechanism by which serotonin can get inside cancer cells and tell them to commit suicide suggests there is a clear " dialogue " between the brain and the immune system, he said. Eli Lilly and Co.'s Prozac, Glaxo SmithKline Plc's Paxil and Lundbeck's Celexa all " substantially blocked " the cancer-killing effects of serotonin. The finding reopens controversy about the widespread use of the class of antidepressants called selective serotonin reuptake inhibitors (SSRIs) that first went on sale in the 1980s. Millions of people with depression and anxiety have been prescribed the drugs, which have emerged as one of the biggest sellers for the international pharmaceutical industry. They work by stopping the " reuptake, " or reabsorption, of serotonin by brain cells. " We've shown that, in the test-tube, the SSRIs stop the action of the serotonin on the cancer cells. But it's nigh on impossible to extrapolate to what's happening in the body, " Gordon told Reuters. " We must stress the effects shown for SSRIs on cancer cells is indirect and should cause no concern whatsoever to the many millions of people throughout the world who are prescribed this class of antidepressants, " he added. A spokesman for Britain's Department of Health said the research was at a very early stage and no increased risk of cancer had been detected. Drug company officials said they did not believe their pills caused any increase in cancer and questioned whether the high doses used in Gordon's experiments may have affected the results. " These data are from an in vitro (test-tube) study and as such they cannot be extrapolated to a clinical setting with any degree of certainty, " said Martin Sutton, a spokesman for GlaxoSmithKline. © 2002 Reuters Limited. All rights reserved. Republication or redistribution of Reuters content, including by framing, linking or similar means, is expressly prohibited without the prior written consent of Reuters. Reuters shall not be liable for any errors or delays in the content, or for any actions taken in reliance thereon. Related News: a.. More news on About Your Medicines b.. More news on Cancer (General) c.. More news on Drug and Medical Device Safety Quote Link to comment Share on other sites More sharing options...
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