EpicentRx, San Diego, CA, USA.
InterWest Partners, Menlo Park, CA, USA.
Expert Opin Ther Targets. 2020 May;24(5):427-438. doi: 10.1080/14728222.2020.1744568. Epub 2020 Apr 12.
: 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.: 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.: TGF-β status may serve as a biomarker to predict responsiveness and as a therapeutic target to increase the activity of immunotherapies.
转化生长因子-β(TGF-β)是许多细胞功能的主要调节剂,包括细胞免疫。在癌症中,TGF-β 可以通过几种机制发挥肿瘤促进作用,包括免疫抑制。由于免疫检查点途径在癌症中被共同选择以诱导 T 细胞耐受,因此本综述假设 TGF-β是癌症中的主要检查点,其负调控影响超过并控制其他免疫检查点。
本综述探讨了靶向 TGF-β及其信号通路的治疗剂,用于治疗癌症,这些治疗剂在最广泛的意义上可归类为检查点抑制剂。这一概念得到了以下观察结果的支持:1)只有一部分患者从当前的检查点抑制剂治疗中获益,2)肿瘤微环境中 TGF-β 的存在与排除或冷肿瘤以及对检查点抑制剂的耐药性相关,以及 3)现有的生物标志物,如 PD-1、PD-L1、微卫星不稳定性和肿瘤突变负担,不足以可靠和充分地识别免疫反应性患者。相比之下,TGF-β 过表达是多种肿瘤类型中广泛存在且具有深远负面影响的分子特征。
TGF-β 状态可作为预测反应性的生物标志物,并作为治疗靶点,以提高免疫疗法的活性。