酪氨酸磷酸化介导的 YAP1-TFAP2A 相互作用协调 HER2+ 乳腺癌的转录和曲妥珠单抗抗药性

IF 15.8 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Hailin Zou , Juan Luo , Yibo Guo , Liang Deng , Leli Zeng , Yihang Pan , Peng Li
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引用次数: 0

摘要

HER2+乳腺癌(BC)的曲妥珠单抗耐药是导致HER2+BC患者预后不良的主要原因。酪氨酸激酶SRC的致癌基因过表达或异常激活被认为是曲妥珠单抗反应的关键调节因子。然而,SRC激活相关的曲妥珠单抗耐药的详细调控机制仍不甚明了。在本研究中,我们发现SRC介导的YAP1酪氨酸磷酸化促进了其与转录因子AP-2 alpha(激活增强子结合蛋白2 alpha,TFAP2A)的相互作用,进而促进了YAP1/TEAD-TFAP2A(YTT)复合物相关的转录输出,从而使HER2+ BC产生曲妥珠单抗耐药。抑制 SRC 激酶活性或破坏 YTT 复合物可使细胞在体外和体内对曲妥珠单抗治疗敏感。此外,我们还发现 YTT 复合物共同占据了一系列与曲妥珠单抗耐药相关基因的调控区域,并直接调控这些基因的转录,包括表皮生长因子受体、HER2、H19 和 CTGF。此外,YTT 介导的转录调控是由 SRC 激酶活性协调的。综上所述,我们的研究揭示了 SRC 介导的 YTT 复合物形成和转录是与曲妥珠单抗耐药相关的多种机制的原因。因此,靶向 HER2 信号与抑制 YTT 相关转录输出相结合,可作为克服 SRC 激活导致的曲妥珠单抗耐药的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tyrosine phosphorylation-mediated YAP1-TFAP2A interactions coordinate transcription and trastuzumab resistance in HER2+ breast cancer

Trastuzumab resistance in HER2+ breast cancer (BC) is the major reason leading to poor prognosis of BC patients. Oncogenic gene overexpression or aberrant activation of tyrosine kinase SRC is identified to be the key modulator of trastuzumab response. However, the detailed regulatory mechanisms underlying SRC activation-associated trastuzumab resistance remain poorly understood. In the present study, we discover that SRC-mediated YAP1 tyrosine phosphorylation facilitates its interaction with transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha, TFAP2A), which in turn promotes YAP1/TEAD-TFAP2A (YTT) complex-associated transcriptional outputs, thereby conferring trastuzumab resistance in HER2+ BC. Inhibition of SRC kinase activity or disruption of YTT complex sensitizes cells to trastuzumab treatment in vitro and in vivo. Additionally, we also identify YTT complex co-occupies the regulatory regions of a series of genes related to trastuzumab resistance and directly regulates their transcriptions, including EGFR, HER2, H19 and CTGF. Moreover, YTT-mediated transcriptional regulation is coordinated by SRC kinase activity. Taken together, our study reveals that SRC-mediated YTT complex formation and transcriptions are responsible for multiple mechanisms associated with trastuzumab resistance. Therefore, targeting HER2 signaling in combination with the inhibition of YTT-associated transcriptional outputs could serve as the treatment strategy to overcome trastuzumab resistance caused by SRC activation.

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来源期刊
Drug Resistance Updates
Drug Resistance Updates 医学-药学
CiteScore
26.20
自引率
11.90%
发文量
32
审稿时长
29 days
期刊介绍: Drug Resistance Updates serves as a platform for publishing original research, commentary, and expert reviews on significant advancements in drug resistance related to infectious diseases and cancer. It encompasses diverse disciplines such as molecular biology, biochemistry, cell biology, pharmacology, microbiology, preclinical therapeutics, oncology, and clinical medicine. The journal addresses both basic research and clinical aspects of drug resistance, providing insights into novel drugs and strategies to overcome resistance. Original research articles are welcomed, and review articles are authored by leaders in the field by invitation. Articles are written by leaders in the field, in response to an invitation from the Editors, and are peer-reviewed prior to publication. Articles are clear, readable, and up-to-date, suitable for a multidisciplinary readership and include schematic diagrams and other illustrations conveying the major points of the article. The goal is to highlight recent areas of growth and put them in perspective. *Expert reviews in clinical and basic drug resistance research in oncology and infectious disease *Describes emerging technologies and therapies, particularly those that overcome drug resistance *Emphasises common themes in microbial and cancer research
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