دورية أكاديمية

Role of PTP1B in HER2 Signaling in Breast Cancer

التفاصيل البيبلوغرافية
العنوان: Role of PTP1B in HER2 Signaling in Breast Cancer
المؤلفون: Saha, Sayanti
المساهمون: INSTITUTE FOR CANCER RESEARCH PHILADELPHIA PA
المصدر: DTIC
سنة النشر: 2012
المجموعة: Defense Technical Information Center: DTIC Technical Reports database
مصطلحات موضوعية: Medicine and Medical Research, BREAST CANCER, EPITHELIUM, RECEPTOR SITES(PHYSIOLOGY), CELLS(BIOLOGY), CLINICAL MEDICINE, CROSSTALK, CYTOPLASM, DRUGS, ENZYMES, IN VITRO ANALYSIS, IN VIVO ANALYSIS, MAMMARY GLANDS, ONCOGENESIS, PHOSPHATASES, PHOSPHORUS TRANSFERASES, PROTEINS, TARGETS, THERAPY, TRACER STUDIES, TYROSINE, SUBSTRATE TRAP, PHOSPHOPROTEOMICS
الوصف: The receptor tyrosine kinase ErbB2 is overexpressed in approximately 25% of all breast cancers. ErbB2, and the signaling pathways it activates, represent potential selective targets for therapy in breast cancer. However, drug resistance is a significant clinical problem with current ErbB2-targeted breast cancer therapies. This is because of our lack of understanding of the molecular mechanism underlying the role of ErbB2 in breast carcinogenesis. Recently, Dr. Chernoff and others have reported that a cytoplasmic enzyme, protein tyrosine phosphatase 1B (PTP1B) plays a positive role in ErbB2-induced breast cancer in vitro and in vivo. Therefore, a detailed understanding of the signaling crosstalk between ErbB2 and PTP1B regulated pathways is warranted. In this research proposal, I have aimed to identify key pro-oncogenic PTP1B regulated pathways in ErbB2 signaling in MCF10A breast epithelial cells using quantitative phosphoproteomics. This study has the potential to uncover novel molecular targets in ErbB2- positive breast cancer and is expected to provide new hope and direction to the present breast cancer biomarkers and therapeutics. ; The original document contains color images.
نوع الوثيقة: text
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اللغة: English
العلاقة: http://www.dtic.mil/docs/citations/ADA579832Test
الإتاحة: http://www.dtic.mil/docs/citations/ADA579832Test
http://oai.dtic.mil/oai/oai?&verb=getRecord&metadataPrefix=html&identifier=ADA579832Test
حقوق: Approved for public release; distribution is unlimited.
رقم الانضمام: edsbas.BC78D22D
قاعدة البيانات: BASE