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Basic Science of Surgical Oncology Sharmila Roy-Chowdhury, M.D. Assistant Professor Division of Surgical Oncology Surgical Oncology Objectives Learn basic information about the science of surgical oncology: Genetic basis of cancer Oncogenes Tumor suppressor genes Tumor markers Chemotherapy agents Surgical Oncology Hereditary mutations Gene changes that come from a parent Exist in all cells of the body, including reproductive cells The mutation can be passed from generation to generation. Also called germline mutations. Accounts for 5% to 10% of cancers Surgical Oncology Acquired mutations Most cancers are caused by acquired mutations. Occurs when DNA in a cell changes during the person’s life. Can be caused by environmental influences such as exposure to radiation or toxins. Not hereditary Sporadic or somatic mutations Surgical Oncology Oncogenes Normal cellular genes (protooncogenes) "picked up" by retroviruses, mutations introduced that cause constitutive activity, and inserted into cells. Gain of function after mutational damage. Divided into four classes Surgical Oncology Oncogenes Surgical Oncology Oncogenes Class I : growth factors PDGF EGF TGFa Surgical Oncology Oncogenes Class II-receptors Cell surface receptors (tyr kinases) fms (CSF-1 R) erbB, neu (EGF R) ros (insulin R) kit (SCF R) met (HGF R) Intracellular receptors erbA (thyroid hormone R) Surgical Oncology Oncogenes Class III-intracellular transducers Protein Tyr kinases Protein Ser/Thr kinases mos, raf G proteins src, yes, fes, abl, ret ras (2nd most commonly altered "oncogene" in human cancer) Phospholipase C crk Surgical Oncology Oncogenes Class IV : nuclear transcription factors jun, fos, myc, myb, ski, rel, p53 Surgical Oncology Tumor Suppressor Genes Defined as any gene whose loss of function leads to tumor progression Block cellular proliferation Surgical Oncology Tumor Suppressor Genes Rb-1 inhibits the transcription factor E2F p53 induces apoptosis of cells with damaged DNA "watchdog" of the genome most commonly altered "oncogene" in human cancer Li-Fraumeni syndrome Surgical Oncology Oncogenes/TSs by Cancer Breast BRCA1/2 HER-2/neu (Epidermal growth factor oncogene) Trastuzumab, Herceptin Surgical Oncology Oncogenes/TSs by Cancer Colon DCC APC responsible for FAP p53 ras MSH/MLH mismatch repair microsatellite instability HNPCC Lynch syndromes Surgical Oncology Oncogenes/TSs by Cancer Pancreas ras p53 MEN men1 (MEN 1) ret (MEN 2A, 2B, heriditary Hirschsprung’s dz) Surgical Oncology Oncogenes/TSs by Cancer GIST c-kit Imatinib, Sunitinib Gleevec, Sutent tyr kinase inhibitors originally designed for use in CML Surgical Oncology Tumor Markers Tumor Markers Type of Cancer PSA Prostate CA CEA Colorectal CA CA 15-3 breast CA CA 19-9 pancreatic CA biliary CA Surgical Oncology Tumor Markers AFP hepatocellular CA testicular CA b-hCG Choriocarcinoma testicular CA 5-HIAA carcinoid Surgical Oncology Tumor Markers Calcitonin Thyroglobulin CA 125 medullary thyroid CA differentiated thyroid CA ovarian CA Gastrin gastrinoma Surgical Oncology Tumor Markers Insulin (with low glucose) PTH (with high Ca) LDH insulinoma parathyroid adenoma/CA testicular CA Melanoma lymphoma Surgical Oncology Chemotherapeutics 5-FU inhibits thymadylate synthase Surgical Oncology Chemotherapeutics Methotrexate inhibits dihydrofolate reductase Surgical Oncology Chemotherapeutics Gemcitabine Cyclophosphamide, ifosfamide, melphalan, mitomycin C, dacarbazine competes with dCTP for DNA incorporation alkylating agents Platinum agents damage DNA by forming adducts Surgical Oncology Chemotherapeutics Adriamycin, topotecan, irinotecan topoisomerase inhibitors Taxol microtubule inhibitor Surgical Oncology Biological Therapeutics Trastuzumab Monoclonal Ab against Her-2/neu Breast CA Rituximab Monoclonal Ab against CD-20 B cell lymphoma Surgical Oncology Biological Therapeutics Cetuximab mAb against EGFR Colon CA Bevacizumab mAb against VEGF Colon CA