BEGIN:VCALENDAR VERSION:2.0 PRODID:-//132.216.98.100//NONSGML kigkonsult.se iCalcreator 2.20.4// BEGIN:VEVENT UID:20260728T170631EDT-2568oIvKOn@132.216.98.100 DTSTAMP:20260728T210631Z DESCRIPTION:Axel A. Thomson\, PhDPrincipal Investigator Research ScientistM RC Human Reproductive Sciences UnitEdinburgh\, UKTitle: Stromal-Epithelial interactions and the regulation of prostate development and cancer – usin g mesenchymal molecules to slow tumour growth   The role of the tumour m icroenvironment in cancer initiation and progression is increasingly recog nized as critically important and yet is poorly understood at the mechanis tic or molecular level. Tumour stroma (cancer associated fibroblasts\, CAF s) stimulate prostate carcinogenesis and stromal histology is an independe nt predictor of prostate cancer patient prognosis. There is considerable i nterest in identifying pathways in tumour stroma that act as paracrine reg ulators of tumour epithelia\, as these may become new therapeutics or diag nostics. Our studies have utilized the similarities between mesenchyme inv olved in directing prostate organogenesis and CAFs involved in tumourigene sis\, since both involve stromal/epithelial interactions and paracrine sig nalling. We have used gene profiling to identify molecules expressed in de velopmental prostate mesenchyme and CAFs\, and focussed upon those which a re secreted or surface bound – since these may function as paracrine regul ators of epithelia (and/or autocrine regulators of stroma). Furthermore\, we have recently demonstrated that we can inhibit the pro-tumourigenic sig nalling of CAFs using the pathways that we identified and characterized in developmental prostatic mesenchyme. This is a novel approach to tumour co ntrol. My approach in regard to studying stromal mechanisms in prostate c ancer is almost unique\, since the majority of research is focussed upon t umour epithelia. We have combined basic developmental biology with tumour studies and used developmental systems to identify and test pathways. Thes e have also been tested in a primary human prostate tumour reconstitution system in which to examine effects upon tumourigenesis via CAFs. This has led us to propose a new paradigm in which developmental mesenchymal pathwa ys can be used to regulate epithelial tumourigenesis by reducing CAF pro-t umourigenic signalling.   DTSTART:20121016T160000Z DTEND:20121016T170000Z SUMMARY:Goodman Cancer Centre Seminar URL:/biochemistry/channels/event/goodman-cancer-centre -seminar-218519 END:VEVENT END:VCALENDAR