School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing, Jiangsu 210094, People's Republic of China; Center for Childhood Cancer and Blood Diseases, The Research Institute at Nationwide Children's Hospital, Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, OH 43205, USA; Chemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, University Town, Wenzhou, Zhejiang 325035, People's Republic of China.
Chemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, University Town, Wenzhou, Zhejiang 325035, People's Republic of China.
Trends Pharmacol Sci. 2016 Jan;37(1):47-61. doi: 10.1016/j.tips.2015.10.001. Epub 2015 Nov 12.
Signal transducer and activator of transcription 3 (STAT3) plays crucial roles in several cellular processes such as cell proliferation and survival, and has been found to be aberrantly activated in many cancers. Much research has explored the leading mechanisms for regulating the STAT3 pathway and its role in promoting tumorigenesis. We focus here on recent evidence suggesting that feedback activation of STAT3 plays a prominent role in mediating drug resistance to a broad spectrum of targeted cancer therapies and chemotherapies. We highlight the potential of co-targeting STAT3 and its primary target to overcome drug resistance, and provide perspective on repurposing clinically approved drugs as STAT3 pathway inhibitors, in combination with the FDA-approved receptor tyrosine kinase (RTK) inhibitors, to improve clinical outcome of cancer treatment.
信号转导子和转录激活子 3(STAT3)在细胞增殖和存活等多种细胞过程中发挥着关键作用,并且在许多癌症中发现其异常激活。大量研究探索了调节 STAT3 途径及其在促进肿瘤发生中的作用的主要机制。我们在这里重点介绍了最近的证据,表明 STAT3 的反馈激活在介导针对广泛的靶向癌症治疗和化疗药物的耐药性中起着突出的作用。我们强调了共同靶向 STAT3 及其主要靶标以克服耐药性的潜力,并就重新利用临床批准的药物作为 STAT3 途径抑制剂,与 FDA 批准的受体酪氨酸激酶(RTK)抑制剂联合使用,以改善癌症治疗的临床结果提供了一些观点。