Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Cancer Biology Course Courses started in 1999; Tuesdays, 12 noon, Farrell Teacher Center, Holden Auditorium All students, postdocs, faculty, staff welcome Alternating years – D Wilson & L Ratner (emphasis on pediatric vs adult oncology WebSite:http://www.siteman.wustl.edu/physician/prof_education/courses_online.shtml Format: 45 min didactic/30 min discussion Schedule for 2008 Course Jan 22 Lee Ratner Introduction Jan 29 Rick Wilson Cancer Genomics Feb 5 Jason Weber mTOR Feb 12 Ron Bose Her2/ErbB signaling Feb 19 Greg Longmore Epithelial-mesenchymal transition Feb 26 John Cooper Cytoskeletal rearrangement in cancer Mar 4 Graham Colditz Breast cancer prevention Mar 12 DPiwnica-Worms Imaging protein-protein interactions Mar 19 John DiPersio Manipulating gvhd Apr 8 Tim Ley NK and T cell anti-tumor activity To Be Scheduled (Mar 26, Apr 1, 15, 22): Rafi Kopan Notch signaling Tej Pandita ATM & DNA Repair Jeff Arbeit HIF-1 and Angiogenesis Lee Ratner NFkB activation in cancer Student-Sponsored Speaker Introduction • History • Epidemiology • Biology • Diagnosis • Treatment • Prevention • Social Issues See Perspectives in Nature Reviews in Cancer Cancer – Historical Perspective 1600 BC Egyptian physician record 1st description of breast cancer 460 BC Hippocrates uses “carcinos” to describe tumors (Greek – crab) 129 AD Galen attributes cancer to black bile 1660 Mastectomy for breast cancer 1713 Ramazzini notes absence of cervical but increased breast ca in nuns 1775 Pott describes scrotal cancer in chimney sweeps 1838 Muller describes cancer as abnormalities of cells 1896 Grubbe administers xrays to cancer patient Cancer – th 20 Century 1903 Radium isolated by Curies used for tumor treatment 1913 American Cancer Society founded 1928 Papanicolau provides basis for PAP smears 1937 Roosevelt creates NCI 1941 Huggins used hormones to treat prostate Ca 1948 Hitchings uses 6MP for childhood leukemia 1955 MTX used for solid tumor 1957 IFN and FU introduced 1966 NCI testing for cancer-causing chemicals 1970 DeVita develops MOPP for Hodgkin Boveri’s Predictions (1902) Cell-cycle checkpoints (Hemmungseinrichtung: inhibitory mechanism) that would allow cell division only when a specific external stimulus is experienced by the cell. The clonal origin of tumours. Genetic mosaicism. Tumour-suppressor genes (Teilungshemmende Chromosomen), the effects of which can be overcome by external signals, and which are physically lost in progressively growing tumours. Oncogenes (Teilungsfoerdernde Chromosomen) that become amplified (im permanenten Übergewicht) during tumour development. Tumour progression from benign to malignant, involving sequential changes of increased growthstimulatory chromosomes and loss of growth-inhibitory chromosomes. Cancer predisposition through inheritance of chromosomes (genes) that are less able to suppress malignancy. Cancer predisposition through inheritance of genes that cause aberrant mitoses. Inheritance of the same 'weak chromosome' from both parents leads to homozygosity for the defective chromosome and, consequently, to high-penetrance cancer syndromes — for example, xeroderma pigmentosum. The role of wounding and inflammation in tumour promotion. Loss of cell adhesion in metastasis. Sensitivity of malignant cells to radiation therapy. Chromosomal Translocations in CML and Solid Tumors 1961-Nowell & Hungerford – Ph chromosome 1972 Rowley t9;22 CML t8;14 Burkitt, t15;17 APL, t11;22 Ewings 1984 – BCR-ABL fusion 1988 – Huang – ATRA 1998 – Druker – Imatinib, Gleevec Acquired Capabilities of Cancer Genetic and epigenetic instability Genomic Landscape of Cancers Estimated proportion of cancer in US that could have been avoided by changes in each category of non-genetic cancer causes – Risk – Structured-data summaries – Meta-analysis – Pooled analysis – Prospective studies – Retrospective studies – Bias – Confounding – Randomized controlled trials – Statistical power Tobacco & Cancer Asbestos & Mesothelioma Radiation & Thyroid Cancer Chernobyl, 1986-10-20m exposed (3.7x1010 Bq = Ci) 1018 Bq 131I and 123I and 132Te->132I; 1017 Bq Cs 1000 vs 30 cases/10 yrs/ 50-90% RET-PTC Atomic bomb – neutrons + gamma rays Cancer Stem Cells Stem cells in adult somatic tissues, Scenarios involving cancer stem cells Multiple Steps to Cancer Reversibility? Epithelial-Mesenchymal Transition Metastasis Paget, 1889 “seed and soil” Signal Transduction by HER family The molecular circuitry of cancer. * * * Apoptosis & Cancer Examples of genetically engineered mouse models that recapitulate human solid cancers Old, 1996 Histological Analysis Grading: tubule formation, pleomorphism, mitoses Clinical vs pathological staging (T, M, N) Gene arrays, miRNA arrays, FISH, CGH, proteomics Even within the same organ, haematoxylin and eosin (H&E) staining can be used to identify tumours with different morphology and prognosis. a | Classical invasive ductal carcinoma of the breast, exhibiting focal glandular differentiation (arrow). b | Invasive and in situ lobular carcinoma, in which the invasive tumour grows in rows of single cells (short arrow). Similar cells are seen within lobular units (long arrow). c | Invasive medullary carcinoma, exhibiting solid sheets of tumour cells (short arrow) and lymphocytic infiltrate at the pushing edge of the tumour (long arrow). d | Invasive micropapillary carcinoma, a rare aggressive type of breast cancer. The tumour is composed entirely of cells that are arranged in small papillary structures. New Linkages in Imaging XRT Surgery Molecular Biology Radiology Molecular Imaging Nanotechnology; BLI Phase I, II, III CR, PR, stable, progressive QoL, DFS, OS, surrogate markers – cancer Ag, PET NCI, FDA, IRB Natural Products periwinkle Pacific yew bark-taxol, microbes – bleo, mitomycin, anthracyclines Marine sources – bryostatin, cytosine arabinoside Enzymatic rxn, binding target, cell killing, high throughput screens Pharmacology Antibodies (Her2, RIT), Tyrosine kinase inhibitors (VEGFR, ABL, KIT); High dose therapy and BMT Also Antibodies – Herceptin, Rituximab Other Tyr kin inhibitors e.g. imatinib (gleevec) High dose therapy, gene therapy, BMT siRNAs Animal models & safety Breast cancer activism Disease advocacy organizations Acquired Capabilities of Cancer Genetic & epigenetic instability Hanahan & Weinberg Cell 100:57-70, 2000 Discussion Paper