Peter M E, Hadji A, Murmann A E, Brockway S, Putzbach W, Pattanayak A, Ceppi P
Division Hematology/Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Cell Death Differ. 2015 Apr;22(4):549-59. doi: 10.1038/cdd.2015.3. Epub 2015 Feb 6.
CD95 (Fas/APO-1) and its ligand, CD95L, have long been viewed as a death receptor/death ligand system that mediates apoptosis induction to maintain immune homeostasis. In addition, these molecules are important in the immune elimination of virus-infected cells and cancer cells. CD95L was, therefore, considered to be useful for cancer therapy. However, major side effects have precluded its systemic use. During the last 10 years, it has been recognized that CD95 and CD95L have multiple cancer-relevant nonapoptotic and tumor-promoting activities. CD95 and CD95L were discovered to be critical survival factors for cancer cells, and were found to protect and promote cancer stem cells. We now discuss five different ways in which inhibiting or eliminating CD95L, rather than augmenting, may be beneficial for cancer therapy alone or in combination with standard chemotherapy or immune therapy.
CD95(Fas/APO-1)及其配体CD95L长期以来被视为一种死亡受体/死亡配体系统,可介导凋亡诱导以维持免疫稳态。此外,这些分子在免疫清除病毒感染细胞和癌细胞方面也很重要。因此,CD95L被认为对癌症治疗有用。然而,严重的副作用使其无法全身应用。在过去十年中,人们认识到CD95和CD95L具有多种与癌症相关的非凋亡和促肿瘤活性。CD95和CD95L被发现是癌细胞的关键生存因子,并被发现可保护和促进癌症干细胞。我们现在讨论五种不同的方式,即抑制或消除CD95L,而非增强它,可能单独或与标准化疗或免疫疗法联合使用时对癌症治疗有益。