Guest guest Posted March 3, 2011 Report Share Posted March 3, 2011 While studying one tumor-suppressing protein, Cheryl 's research team at The University of Texas MD Cancer Center came across a separate surprise. They found another protective protein known to work inside the cell nucleus moonlighting out in the cell's cytoplasm. Following up on this unexpected observation, they discovered the cancer-blocking nuclear protein ATM has a second job controlling and killing damaged cells in the area between the nucleus and the cell membrane. Both functions stymie cancer by preventing reproduction of defective cells. http://www.medicalnewstoday.com/articles/217341.php *************************** Blood clots in the leg (deep vein thrombosis DVT) occur commonly. In one-half of the cases, the blood clot will break loose and travel through the bloodstream to the lungs which may be life-threatening. Current treatment stops the blood clot from moving, but does not prevent permanent damage to the vein. Many patients may suffer long-term swelling and pain in their legs. Today, patients are normally treated with the blood-thinning medication warfarin and must wear support hose for two years. A project led by Dr Per Morten Sandset, a professor at Oslo University Hospital, and funded under the Research Programme on Clinical Research (KLINISKFORSKNING) at the Research Council will examine whether patients will benefit from additional treatment with drugs that dissolve blood clots (a treatment called thrombolysis). http://www.medicalnewstoday.com/articles/217734.php ******************************************* Like a switch stuck in the on position, the bone marrow can churn out blood cells that bloat internal organs and clog blood vessels, leading to life-threatening disease. Now University of Florida scientists have discovered a potential new drug that can throw the switch on the runaway blood cell-production mechanism. The drug shrinks cell-gorged organs and stems the overproduction of blood cells, and the researchers are working toward bringing it into clinical trial in one year. " The disease has a path it's going to take and you need to be able to alter that path - our drug does that to a reasonable extent, " said P. Sayeski, Ph.D., an associate professor of physiology and functional genomics in the UF College of Medicine, who led the research team. http://www.medicalnewstoday.com/articles/217540.php ********************************* FYI, Lottie Duthu Quote Link to comment Share on other sites More sharing options...
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