ShcD 适应蛋白通过表皮生长因子受体信号的异常激活驱动三阴性乳腺癌细胞的侵袭。

IF 6.6 2区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Hayley R Lau, Hayley S Smith, Begüm Alural, Claire E Martin, Laura A New, Manali Tilak, Sara L Banerjee, Hannah N Robeson, Nicolas Bisson, Anne-Claude Gingras, Jasmin Lalonde, Nina Jones
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引用次数: 0

摘要

三阴性乳腺癌(TNBC)是高度转移的,由于缺乏靶向治疗,给临床带来了挑战。在这里,我们报告了ShcD磷酸酪氨酸衔接蛋白在TNBC中上调,其表达与患者总体生存率降低和化疗反应降低相关。在人乳腺癌细胞中,我们证明了ShcD表达促进细胞侵袭并减少粘附,而这些作用通过突变ShcD磷酸酪氨酸结合(PTB)结构域而被消除。同样,在三维组装体模型中,来自脑转移性TNBC细胞的表达shcd的球体对脑类器官的浸润增强。利用蛋白质组学筛选ShcD结合伙伴,我们确定了表皮生长因子受体(EGFR)信号的多种成分,并确认这些成分与ShcD而不是PTB突变体相互作用。有趣的是,ShcD相互作用组与EGFR酪氨酸激酶抑制剂耐药性相关,这与我们的研究结果一致,即ShcD过表达导致EGFR过度磷酸化,而ShcD敲除或PTB突变可恢复这种反应。最后,在TNBC细胞中使用吲哚美辛对ShcD PTB结构域进行药理学抑制可减少EGFR结合和过度磷酸化,并减少细胞侵袭。总之,我们的研究结果确定了ShcD是TNBC转移的潜在因素,并为临床靶向接头蛋白提供了分子基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ShcD adaptor protein drives invasion of triple negative breast cancer cells by aberrant activation of EGFR signaling.

Triple-negative breast cancer (TNBC) is highly metastatic and presents clinical challenges given the lack of targeted therapies. Here, we report that the ShcD phosphotyrosine adaptor protein is upregulated in TNBC, and its expression correlates with overall reduced patient survival and decreased response to chemotherapy. In human breast cancer cells, we demonstrate that ShcD expression promotes cell invasion and reduces adhesion, and that these effects are abrogated by mutating the ShcD phosphotyrosine binding (PTB) domain. Similarly, in a three-dimensional assembloid model, ShcD-expressing spheroids derived from brain metastatic TNBC cells show enhanced infiltration into cerebral organoids. Using a proteomic screen for ShcD binding partners, we identify multiple components of epidermal growth factor receptor (EGFR) signaling and confirm these interactions with ShcD but not the PTB mutant. Interestingly, the ShcD interactome correlates with EGFR tyrosine kinase inhibitor resistance, in line with our findings that ShcD overexpression results in hyperphosphorylation of EGFR while ShcD knockout or PTB mutation reverts this response. Lastly, pharmacological inhibition of the ShcD PTB domain using indomethacin in TNBC cells decreases EGFR binding and hyperphosphorylation and reduces cell invasion. Altogether, our results identify ShcD as a potential contributor to metastasis in TNBC, and they provide a molecular basis for clinical targeting of adaptor proteins.

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来源期刊
Molecular Oncology
Molecular Oncology Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
11.80
自引率
1.50%
发文量
203
审稿时长
10 weeks
期刊介绍: Molecular Oncology highlights new discoveries, approaches, and technical developments, in basic, clinical and discovery-driven translational cancer research. It publishes research articles, reviews (by invitation only), and timely science policy articles. The journal is now fully Open Access with all articles published over the past 10 years freely available.
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