| Literature DB >> 35181272 |
Jitka Fucikova1, Lenka Palova-Jelinkova2, Vanessa Klapp3, Peter Holicek4, Tereza Lanickova4, Lenka Kasikova5, Jana Drozenova6, David Cibula7, Beatriz Álvarez-Abril8, Elena García-Martínez9, Radek Spisek4, Lorenzo Galluzzi10.
Abstract
At odds with other solid tumors, epithelial ovarian cancer (EOC) is poorly sensitive to immune checkpoint inhibitors (ICIs), largely reflecting active immunosuppression despite CD8+ T cell infiltration at baseline. Accumulating evidence indicates that both conventional chemotherapeutics and targeted anticancer agents commonly used in the clinical management of EOC not only mediate a cytostatic and cytotoxic activity against malignant cells, but also drive therapeutically relevant immunostimulatory or immunosuppressive effects. Here, we discuss such an immunomodulatory activity, with a specific focus on molecular and cellular pathways that can be harnessed to develop superior combinatorial regimens for clinical EOC care.Entities:
Keywords: PARP inhibitors; antiangiogenic agents; bevacizumab; immunogenic cell death; platinum derivatives; taxanes
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Year: 2022 PMID: 35181272 DOI: 10.1016/j.trecan.2022.01.010
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025