肿瘤微环境
间质细胞
卵巢癌
转录组
癌症研究
化疗
生物
医学
癌症
免疫学
内科学
基因
基因表达
肿瘤细胞
生物化学
作者
Eleni Maniati,Chiara Berlato,Ganga Gopinathan,Owen Heath,Panoraia Kotantaki,Anissa Lakhani,Jacqueline McDermott,Colin Pegrum,Robin Delaine-Smith,Oliver M.T. Pearce,Priyanka Hirani,Joash D. Joy,Ludmila Szabova,Ruth Perets,Owen J. Sansom,Ronny Drapkin,Peter J. Bailey,Frances R. Balkwill
出处
期刊:Cell Reports
[Elsevier]
日期:2020-01-01
卷期号:30 (2): 525-540.e7
被引量:60
标识
DOI:10.1016/j.celrep.2019.12.034
摘要
Although there are many prospective targets in the tumor microenvironment (TME) of high-grade serous ovarian cancer (HGSOC), pre-clinical testing is challenging, especially as there is limited information on the murine TME. Here, we characterize the TME of six orthotopic, transplantable syngeneic murine HGSOC lines established from genetic models and compare these to patient biopsies. We identify significant correlations between the transcriptome, host cell infiltrates, matrisome, vasculature, and tissue modulus of mouse and human TMEs, with several stromal and malignant targets in common. However, each model shows distinct differences and potential vulnerabilities that enabled us to test predictions about response to chemotherapy and an anti-IL-6 antibody. Using machine learning, the transcriptional profiles of the mouse tumors that differed in chemotherapy response are able to classify chemotherapy-sensitive and -refractory patient tumors. These models provide useful pre-clinical tools and may help identify subgroups of HGSOC patients who are most likely to respond to specific therapies.
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