调节器
主调节器
免疫系统
免疫检查点
肿瘤微环境
癌症研究
癌症
免疫疗法
转化生长因子
细胞生物学
生物
转化生长因子β
免疫耐受
癌症免疫疗法
免疫抑制
免疫学
医学
遗传学
转录因子
基因
作者
Christopher Larson,Bryan Oronsky,Corey A. Carter,Arnold L. Oronsky,Susan J. Knox,David J. Sher,Tony R. Reid
标识
DOI:10.1080/14728222.2020.1744568
摘要
Introduction: Transforming Growth Factor-Beta (TGF-β) is a master regulator of numerous cellular functions including cellular immunity. In cancer, TGF-β can function as a tumor promoter via several mechanisms including immunosuppression. Since the immune checkpoint pathways are co-opted in cancer to induce T cell tolerance, this review posits that TGF-β is a master checkpoint in cancer, whose negative regulatory influence overrides and controls that of other immune checkpoints.Areas Covered: This review examines therapeutic agents that target TGF-β and its signaling pathways for the treatment of cancer which may be classifiable as checkpoint inhibitors in the broadest sense. This concept is supported by the observations that 1) only a subset of patients benefit from current checkpoint inhibitor therapies, 2) the presence of TGF-β in the tumor microenvironment is associated with excluded or cold tumors, and resistance to checkpoint inhibitors, and 3) existing biomarkers such as PD-1, PD-L1, microsatellite instability and tumor mutational burden are inadequate to reliably and adequately identify immuno-responsive patients. By contrast, TGF-β overexpression is a widespread and profoundly negative molecular hallmark in multiple tumor types.Expert Opinion: TGF-β status may serve as a biomarker to predict responsiveness and as a therapeutic target to increase the activity of immunotherapies.
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