Division of Hematology and Oncology, Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, USA.
J Hematol Oncol. 2021 Apr 6;14(1):55. doi: 10.1186/s13045-021-01053-x.
The TGF-β signaling pathway governs key cellular processes under physiologic conditions and is deregulated in many pathologies, including cancer. TGF-β is a multifunctional cytokine that acts in a cell- and context-dependent manner as a tumor promoter or tumor suppressor. As a tumor promoter, the TGF-β pathway enhances cell proliferation, migratory invasion, metastatic spread within the tumor microenvironment and suppresses immunosurveillance. Collectively, the pleiotropic nature of TGF-β signaling contributes to drug resistance, tumor escape and undermines clinical response to therapy. Based upon a wealth of preclinical studies, the TGF-β pathway has been pharmacologically targeted using small molecule inhibitors, TGF-β-directed chimeric monoclonal antibodies, ligand traps, antisense oligonucleotides and vaccines that have been now evaluated in clinical trials. Here, we have assessed the safety and efficacy of TGF-β pathway antagonists from multiple drug classes that have been evaluated in completed and ongoing trials. We highlight Vactosertib, a highly potent small molecule TGF-β type 1 receptor kinase inhibitor that is well-tolerated with an acceptable safety profile that has shown efficacy against multiple types of cancer. The TGF-β ligand traps Bintrafusp alfa (a bifunctional conjugate that binds TGF-β and PD-L1), AVID200 (a computationally designed trap of TGF-β receptor ectodomains fused to an Fc domain) and Luspatercept (a recombinant fusion that links the activin receptor IIb to IgG) offer new ways to fight difficult-to-treat cancers. While TGF-β pathway antagonists are rapidly emerging as highly promising, safe and effective anticancer agents, significant challenges remain. Minimizing the unintentional inhibition of tumor-suppressing activity and inflammatory effects with the desired restraint on tumor-promoting activities has impeded the clinical development of TGF-β pathway antagonists. A better understanding of the mechanistic details of the TGF-β pathway should lead to more effective TGF-β antagonists and uncover biomarkers that better stratify patient selection, improve patient responses and further the clinical development of TGF-β antagonists.
TGF-β 信号通路在生理条件下控制着关键的细胞过程,并且在许多病理学中失调,包括癌症。TGF-β 是一种多功能细胞因子,以细胞和上下文依赖的方式作为肿瘤促进剂或肿瘤抑制剂发挥作用。作为肿瘤促进剂,TGF-β 途径增强细胞增殖、迁移侵袭、肿瘤微环境中的转移扩散,并抑制免疫监视。总之,TGF-β 信号的多效性有助于药物耐药性、肿瘤逃逸,并破坏对治疗的临床反应。基于大量的临床前研究,已经使用小分子抑制剂、靶向 TGF-β 的嵌合单克隆抗体、配体陷阱、反义寡核苷酸和疫苗对 TGF-β 途径进行了药理学靶向治疗,这些已经在临床试验中进行了评估。在这里,我们评估了已在已完成和正在进行的试验中评估的来自多种药物类别的 TGF-β 途径拮抗剂的安全性和疗效。我们重点介绍了 Vactosertib,这是一种高效的小分子 TGF-β 型 1 受体激酶抑制剂,具有良好的耐受性和可接受的安全性,已显示出对多种类型癌症的疗效。TGF-β 配体陷阱 Bintrafusp alfa(一种结合 TGF-β 和 PD-L1 的双功能缀合物)、AVID200(一种融合 TGF-β 受体外域与 Fc 域的计算设计陷阱)和 Luspatercept(一种将激活素受体 IIb 与 IgG 连接的重组融合物)提供了对抗难治性癌症的新方法。虽然 TGF-β 途径拮抗剂作为极具前途、安全有效的抗癌药物正在迅速出现,但仍存在重大挑战。在对肿瘤促进活性进行所需限制的同时,最大限度地减少对肿瘤抑制活性和炎症作用的非故意抑制,阻碍了 TGF-β 途径拮抗剂的临床开发。对 TGF-β 途径的机制细节有了更好的理解,应该会导致更有效的 TGF-β 拮抗剂,并发现更好地分层患者选择、提高患者反应并进一步推进 TGF-β 拮抗剂临床开发的生物标志物。