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Ovarian cancer is the most deadly cancer of the female reproductive system. In 2009, it is estimated that this cancer alone will have claimed 14,600 American women's lives. Often known as "the silent killer," ovarian cancer is difficult to detect early because the ovaries are deep within the pelvis and initial symptoms are often ambiguous. Too often the cancer goes undiagnosed until after the disease is far advanced and has spread throughout the abdomen or to distant organs. After the cancer has metastasized, survival rates plummet because the current treatments are largely ineffective in fighting late stage ovarian cancer. More effective treatments and better early detection tools must be developed to meet the unmet needs of ovarian cancer patients and save their lives. The National Foundation for Cancer Research funds an array of research projects conducted by leading scientists in the field of ovarian cancer research. Through their innovative and diversified approaches to developing new models for ovarian cancer treatment; finding ways to enhance the treatment efficacy of standard chemotherapy; discovering and developing gene therapies that suppress tumor metastasis; and collecting and annotating precious ovarian tumor tissues for developing early detection tools, these NFCR-funded scientists are gaining momentum in the battle against the most deadly gynecologic cancer of our time. Listed below are some notable ovarian cancer research programs that NFCR currently supports. TARGETING OVARIAN CANCER Developing a New Model for Ovarian Cancer Treatment Ovarian cancer continues to claim the lives of three out of four women with the disease, due mainly to the persistence of drug-resistant cancer cells that survive despite standard chemotherapy. These resistant cancer cells can remain dormant or "asleep" for years, only to awaken later and grow progressively until they cause the death of the patient. A key to understanding and perhaps killing off dormant ovarian cancer cells may lie in a recent discovery by NFCR Project Director Robert C. Bast, Jr., M.D. Dr. Bast and his research team at the M.D. Anderson Cancer Center found a gene called ARHI, which plays a critical role in the survival of dormant cancer cells. The team further developed a new experimental model in which ARHI can be switched on and off to closely mimic the actual tumor dormancy and regrowth that occurs in humans. This model will help cancer researchers understand the molecular mechanism of cell dormancy and open the door to the development of new treatments that eliminate these cells before they can become reactivated in the body. In addition, because of the similarities between this new model and the actual disease in humans, new therapeutics can be rapidly moved into clinical trials to treat ovarian cancer patients and give them renewed hope. Making Taxol Work More Effectively Paclitaxel, better known by its brand name, Taxol®, is one of the most widely used chemotherapy drugs in the world. It has been used to treat over a million cancer patients with ovarian, breast, and lung cancer. But Taxol is not a magic bullet - it gradually loses its effectiveness as tumors develop resistance to it during treatment. Internationally renowned for her discovery of the molecular mechanism of Taxol, NFCR Fellow Susan Band Horwitz, Ph.D., at the Albert Einstein College of Medicine, is now exploring why tumor resistance to Taxol occurs and how to make the drug work better. Dr. Horwitz reasoned that during chemotherapy treatment, tumor cells may activate a protective molecular pathway which renders tumors resistant to Taxol. Once she had confirmed that alternate pathway, she proposed a combinatory drug approach in which a second drug is used to inhibit the activated molecular pathway and make the tumor cells regain sensitivity to Taxol. This rational combination strategy turned out to be very effective in experiments with tumor models, and may soon enter clinical trials with cancer patients to confirm its value as a treatment option. Stopping Cancer's Lethal Spread Two-thirds of ovarian cancer cases are diagnosed when the disease has already spread throughout the abdomen and to distant organs, and only 30% of women with late stage ovarian cancer now survive five years or longer. Very little is known about how cancer cells spread to distant sites in the body and many researchers have shied away from the complex biology of metastatic cancer. At the NFCR Center for Metastatic Research, the Center Director Danny Welch, Ph.D., and his collaborators from five universities across the United States are opening the research doors to an understanding of the metastatic process. They have discovered six "metastasis suppressor genes" including the BRMS1 gene found in metastatic breast and ovarian cancer. Using cancer cell lines and DNA chip technology (microarray), they are identifying molecular factors (microRNAs) which may mediate the suppression of cancer metastasis by BRMS1. The impact of this research is enormously significant as it could lead to novel anti-cancer therapies that prevent breast and ovarian cancer from spreading to distant organs, bringing the cancer under control and giving patients increased likelihood of long term survival. NFCR is Fighting Ovarian Cancer on a Global Scale Striving to Escalate Support for Research on Early Detection of Ovarian Cancer Earlier is better, and for ovarian cancer, this is especially true. Until now, there hasn't been a reliable test available for early detection of ovarian cancer so only 19% of all cases are detected at an early, more treatable stage. A great deal of research is needed to discover new and more reliable biomarkers as an essential "next step" in improving early detection of this disease. It is our sincere hope that, with additional funding, NFCR will be able to expand support for research in this important area. NFCR Project Director Robert C. Bast, Jr., M.D., is a world leader in the field of ovarian cancer early detection. In 1981, Dr. Bast discovered CA125, currently the most accurate marker for detecting early signs of ovarian cancer in the blood. In addition to his notable work, supported by NFCR, on developing more effective treatment for chemotherapy- resistant ovarian cancer, Dr. Bast and his research team continue to work on CA125 and other potential biomarkers to optimize the strategies for early detection of ovarian cancer. More funding from NFCR will surely help Dr. Bast raise his promising research on early detection to the next level, making it possible, down the road, for more women to win their race against this deadly disease. NEXT STEPS: HOW YOU CAN HELP
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