BEGIN:VCALENDAR VERSION:2.0 PRODID:-//132.216.98.100//NONSGML kigkonsult.se iCalcreator 2.20.4// BEGIN:VEVENT UID:20251005T205547EDT-9941ckEx7d@132.216.98.100 DTSTAMP:20251006T005547Z DESCRIPTION:Ovarian cancer is the fifth largest cause of cancer-related dea ths in women. The vast majority of ovarian cancers are epithelial ovarian cancers and high-grade serous carcinoma (HGSC) is the most common and most lethal epithelial ovarian cancer. In the last 10 years\, it has been reco gnized that the cell of origin of most HGSCs is within the fallopian tube epithelium\, instead of the ovarian surface epithelium. However\, the earl y events in disease progression still remain poorly defined\, because HGSC is usually diagnosed at advanced stages and lack of proper animal models recapitulating human disease progression.\n\nMy group has recently develop ed a unique strategy for generating mouse ovarian cancer models\, which is a combination of in vivo fallopian tube electroporation\, Cre-mediated li neage tracing and CRISPR-mediated gene modifications. As proof-of-principl e\, we generated a highly metastatic HGSC model by targeting four tumor su ppressor genes. The female mice targeted these four genes generated ovaria n tumors within 5 months after electroporation and peritoneal metastasis w ithin 6 months. After 6 months\, ascites formation was observed in two thi rd of those females. Interestingly\, similar to human ovarian cancer patie nts\, we observed two metastatic patterns\, miliary and non-miliary.\n\nOu r unique strategy has several advantages over the current mouse cancer mod els\; 1) High flexibility permitting many gene combinations/modifications and host genetic backgrounds to be tested\; 2) Control over the size and a rea of targeted cells (the low-frequency mosaic transfection pattern bette r recapitulates the sporadic nature of human tumorigenesis)\; 3) The abili ty to track genetically modified cells by fluorescent reporters\, permitti ng analysis of tumor initiation and early metastasis\; 4) Highly metastati c mouse models with immune competency.\n DTSTART:20190927T150000Z DTEND:20190927T160000Z LOCATION:Room 1034\, McIntyre Medical Building\, CA\, QC\, Montreal\, H3G 1 Y6\, 3655 promenade Sir William Osler SUMMARY:Seminar - Modeling ovarian cancer in mice using in vivo electropora tion and CRISPR mediated genome editing URL:/physiology/channels/event/seminar-modeling-ovaria n-cancer-mice-using-vivo-electroporation-and-crispr-mediated-genome-editin g-299670 END:VEVENT END:VCALENDAR