Public release date: 21-Jun-2012 [ | E-mail | Share ] <\/p>\n
Contact: Crislyn-D'Souza-Schorey cdsouzas@nd.edu<\/a> 574-631-3735 University of Notre Dame<\/p>\n A new paper by Crislyn D'Souza-Schorey, professor of biological sciences at the University of Notre Dame, discusses the biology of tumor-derived microvesicles and their clinical application as circulating biomarkers. Microvesicles are membrane-bound sacs released by tumor cells and can be detected in the body fluids of cancer patients. <\/p>\n The World Health Organization (WHO) estimates that the incidence of cancer will reach approximately 9 million deaths in 2015. The rising prevalence of the disease is a major factor that drives the growth of the oncology biomarkers market. Biomarkers can be defined as any biological, chemical or physical parameter that can be utilized as an indicator of physiological or disease status. Thus, biomarkers are useful in cancer screening and detection, drug design and also to boost the effectiveness of cancer care by allowing physicians to tailor therapies for individual patientsan approach known as personalized medicine. <\/p>\n The new paper discusses the potential of microvesicles to present a combination of disease and tissue-specific markers that would constitute a unique, specific and identifiable biosignature for individual cancers. <\/p>\n \"As such, it would make their sampling over time a preferred method to monitor changes to the tumor in response to treatment, especially for tissues such as the ovary or pancreas, where repeated biopsies of these organs is impractical,\" D'Souza-Schorey said. <\/p>\n Profiling of microvesicles could form the basis of personalized, targeted cancer therapies, especially as more reliable and rapid profiling technologies become available. <\/p>\n \"For example, certain markers like HER2\/neu, in addition to being elevated in breast cancer, is also increased in a relatively smaller subset of other cancers such as ovarian cancer,\" D'Souza-Schorey said. \"This latter group of patients would benefit from existing treatment strategies that target the HER2 receptor.\" <\/p>\n The approach could be advantageous over currently used approaches of profiling whole tissue or un-fractionated body fluid particularly if circulating microvesicles indeed concentrate molecular changes that occur in the tumor, as it would increase the sensitivity of detecting critical markers of cancer progression. <\/p>\n \"One complicating factor, though, is the presence of shed vesicles from other non-tumor cell types also in direct contact with these body fluids,\" D'Souza-Schorey said. \"Thus, equally significant is the development of strategies to selectively capture tumor-specific markers that separate from other shed vesicle populations.\" <\/p>\n<\/p>\n Read more: Public release date: 21-Jun-2012 [ | E-mail | Share ] Contact: Crislyn-D'Souza-Schorey cdsouzas@nd.edu<\/a> 574-631-3735 University of Notre Dame A new paper by Crislyn D'Souza-Schorey, professor of biological sciences at the University of Notre Dame, discusses the biology of tumor-derived microvesicles and their clinical application as circulating biomarkers. Microvesicles are membrane-bound sacs released by tumor cells and can be detected in the body fluids of cancer patients. The World Health Organization (WHO) estimates that the incidence of cancer will reach approximately 9 million deaths in 2015 Continue reading
\nNotre Dame researcher's paper examines the biology of tumor-derived microvesicles<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"