Department of Oncology, The Affiliated Lianyungang Hospital of Xuzhou Medical University, No.182, Tongguan Road, Lianyungang City 222002, Jiangsu Province, China.
Department of Oncology, Lianyungang Clinical Medical College of Nanjing Medical University, No.182, Tongguan Road, Lianyungang City 222002, Jiangsu Province, China.
Biomed Pharmacother. 2020 Nov;131:110557. doi: 10.1016/j.biopha.2020.110557. Epub 2020 Aug 21.
Antiangiogenic drugs have become a standard therapeutic regimen for advanced non-small cell lung cancer (NSCLC); however, many issues remain to be solved. Identifying specific markers to predict patient response to antiangiogenic drugs to ensure therapeutic efficacy would increase their clinical benefit. MicroRNAs (miRNAs) are involved in the process of resistance to antiangiogenic therapy, as they regulate various key signaling pathways. Therefore, miRNAs may be used as targets for reversing tumor resistance to antiangiogenic therapy. This article reviews the molecular mechanisms of antiangiogenic therapy resistance and the specific mechanisms of miRNA regulation of resistance. Signal transducer and activator of transcription 3 (STAT3) is one of multiple target genes of miRNAs, and is closely related to antiangiogenic research. Thus, it is described separately in this review article.
抗血管生成药物已成为晚期非小细胞肺癌(NSCLC)的标准治疗方案;然而,仍有许多问题亟待解决。确定预测患者对抗血管生成药物反应的特定标志物,以确保治疗效果,将增加其临床获益。microRNAs(miRNAs)参与抗血管生成治疗的耐药过程,因为它们调节各种关键信号通路。因此,miRNAs 可能被用作逆转肿瘤对抗血管生成治疗耐药的靶点。本文综述了抗血管生成治疗耐药的分子机制以及 miRNA 调节耐药的具体机制。信号转导和转录激活因子 3(STAT3)是 miRNA 的多个靶基因之一,与抗血管生成研究密切相关。因此,在本文综述中单独进行了描述。