SRGN crosstalks with YAP to maintain chemoresistance and stemness in breast cancer cells by modulating HDAC2 expression

基因敲除 癌症研究 异位表达 交易激励 乳腺癌 生物 微阵列分析技术 转录因子 流式细胞术 癌症 基因表达 分子生物学 细胞培养 基因 遗传学
作者
Zhijie Zhang,Ni Qiu,Jiang Yin,Jianlei Zhang,Hao Liu,Wei Guo,Meijun Liu,Ting Liu,Danyang Chen,Kai Luo,Hongsheng Li,Zhimin He,Jinbao Liu,Guopei Zheng
出处
期刊:Theranostics [Ivyspring International Publisher]
卷期号:10 (10): 4290-4307 被引量:67
标识
DOI:10.7150/thno.41008
摘要

Background: Chemoresistance is a significant obstacle to the effective treatment of breast cancer (BC), resulting in more aggressive behavior and worse clinical outcome.The molecular mechanisms underlying breast cancer chemoresistance remain unclear.Our microarray analysis had identified the overexpression of a small molecular glycoprotein serglycin (SRGN) in multidrug-resistant BC cells.Here, we aimed to investigate the role of SRGN in chemoresistance of breast cancer and elucidate the underlying mechanisms.Methods: SRNG overexpression was identified using microarray analysis and its clinical relevance was analyzed.To investigate the role of SRGN, we performed various in vitro and in vivo studies, as well as characterization of serum and tissue samples from BC patients.Chemosensitivity measurement, gene expression interference, immunofluorescence staining, mammosphere assay, flow cytometry analysis, luciferase reporter assay, ChIP-qPCR, coimmunoprecipitation, and immunohistochemistry were performed to explore the potential functions and mechanisms of SRGN.Results: We confirmed overexpression of SRGN in chemoresistant BC cells and in serum and tissue samples from BC patients with poor response to chemotherapy.SRGN specifically predicted poor prognosis in BC patients receiving chemotherapy.Mechanistically, SRGN promoted chemoresistance both in vitro and in vivo by cross-talking with the transcriptional coactivator YES-associated protein (YAP) to maintain stemness in BC cells.Ectopic YAP expression restored the effects of SRGN knockdown.Inversely, YAP knockdown rescued the effects of SRGN overexpression.The secreted SRGN triggered ITGA5/FAK/CREB signaling to enhance YAP transcription.Reciprocally, YAP promoted SRGN transcription in a TEAD1-dependent manner to form a feed-forward circuit.Moreover, the YAP/RUNX1 complex promoted HDAC2 transcription to induce chemoresistance and stemness in BC cells.Importantly, the SRGN levels were positively correlated with the YAP and HDAC2 levels in chemoresistant BC tissues.YAP and HDAC2 acted downstream of SRNG and correlated with poor outcomes of BC patients receiving chemotherapy. Ivyspring
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