Guest guest Posted March 6, 2011 Report Share Posted March 6, 2011 In a study in the Journal of the National Cancer Institute, researchers from the Institute of Cancer Research (ICR) found that Sprycel, known generically as dasatinib and already used in other cancers, reduced bowel cancer cell growth in the lab by blocking the effects of an enzyme called lysyl oxidase, or LOX. " The enzyme LOX is the one that is important for the cancer to spread, and if you block that then you can stop the cancer from growing, " Janine Erler, who led the study, said in an interview. Erler said this followed previous work in which her team found LOX played a role in the spread of breast cancer, leading them to suspect it may also be key in other tumors. The latest study confirmed LOX was also important in bowel cancer growth and spread, Erler said, and showed cell growth increases in tumor cells with high levels of LOX, while low levels of LOX lead to limited cell growth. The team also showed LOX was activating a molecule called SRC to promote cancer growth and spread - a finding that led them to look at Sprycel, which is known to block SRC function and is already being used to treat patients with chronic myeloid leukemia, or CML. Pfizer's bosutinib, which is currently in late stage trials for CML, is also known to block SRC, as is Ariad's ponatinib, which is undergoing mid-stage testing. Read more on this.......... http://tinyurl.com/63u7ob3 *************************************** Only 10% of Gleevec Patients Eligible for Interruption of Treatment " Sustained deep molecular remission, as we have used as an entry criteria for this trial, is not a frequent outcome of imatinib treatment, " Francois-Xavier Mahon of Universite Victor Segalen Bordeaux and colleagues reported. " Therefore, patients treated with imatinib who are candidates for treatment interruption are rare ... (and) might represent 10 percent of patients. " Commenting on the findings, Valent of the Medical University of Vienna said the results showed there was now hope for a drug-induced cure in CML, although questions remained as to whether most patients could be cured and what drugs or combinations of drugs were needed. http://tinyurl.com/283837m ************************************ The Downside to Osteoporosis Drugs According to a study published in the Journal of the American Medical Association, long-term use of the osteoporosis drugs known as bisphosphonates may increase the risk of unusual types of femur fractures. The risk of these unusual fractures remains low, however, and should be balanced against the established benefits of bisphosphonates, which include a reduction in the risk of hip fractures. Osteoporosis—a condition characterized by low bone mass and deterioration of bone structure—affects an estimated 10 million Americans over the age of 50. Each year, roughly 1.5 million Americans will experience an osteoporosis-related bone fracture. These fractures commonly involve the wrist, hip, or spine, but can affect any part of the body. Drugs that may be used to treat osteoporosis include bisphosphonates (such as Fosamax® [alendronate], Actonel® [risedronate], Boniva® [ibandronate], and Reclast® [zoledronic acid]), Prolia® (denosumab), calcitonin, estrogen, Evista® (raloxifene), and Forteo® (teriparatide). Treatment of osteoporosis reduces the risk of fracture, including hip fracture. Hip fractures occur in the upper part of the femur (the thigh bone) and are an important cause of disability and death in the elderly. Read more....... Source: Bisphosphonate use and the risk of subtrochanteric or femoral shaft fractures in older women. JAMA. 2011;305:783-789. http://tinyurl.com/4g2ydfy FYI, Lottie Duthu Quote Link to comment Share on other sites More sharing options...
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