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通过靶向 STAT3 抑制克服癌症治疗的获得性耐药性。

Overcoming Acquired Drug Resistance to Cancer Therapies through Targeted STAT3 Inhibition.

机构信息

Singh Biotechnology, 1547 Fox Grape Loop, Lutz, FL 33558, USA.

Department of Cell Biology, Microbiology and Molecular Biology, University of South Florida, Tampa, FL 33620, USA.

出版信息

Int J Mol Sci. 2023 Mar 1;24(5):4722. doi: 10.3390/ijms24054722.

Abstract

Anti-neoplastic agents for cancer treatment utilize many different mechanisms of action and, when combined, can result in potent inhibition of cancer growth. Combination therapies can result in long-term, durable remission or even cure; however, too many times, these anti-neoplastic agents lose their efficacy due to the development of acquired drug resistance (ADR). In this review, we evaluate the scientific and medical literature that elucidate STAT3-mediated mechanisms of resistance to cancer therapeutics. Herein, we have found that at least 24 different anti-neoplastic agents-standard toxic chemotherapeutic agents, targeted kinase inhibitors, anti-hormonal agents, and monoclonal antibodies-that utilize the STAT3 signaling pathway as one mechanism of developing therapeutic resistance. Targeting STAT3, in combination with existing anti-neoplastic agents, may prove to be a successful therapeutic strategy to either prevent or even overcome ADR to standard and novel cancer therapies.

摘要

用于癌症治疗的抗肿瘤药物利用许多不同的作用机制,联合使用时可以有效地抑制癌症生长。联合治疗可以导致长期、持久的缓解甚至治愈;然而,抗肿瘤药物的疗效常常因获得性耐药(ADR)的发展而丧失。在这篇综述中,我们评估了阐明 STAT3 介导的癌症治疗耐药机制的科学和医学文献。在此,我们发现至少有 24 种不同的抗肿瘤药物——标准毒性化疗药物、靶向激酶抑制剂、抗激素药物和单克隆抗体——将 STAT3 信号通路作为产生治疗耐药性的一种机制。靶向 STAT3,与现有的抗肿瘤药物联合使用,可能是一种成功的治疗策略,可以预防甚至克服标准和新型癌症治疗的 ADR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7e9/10002572/b7e03a8bba0d/ijms-24-04722-g001.jpg

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