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