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分泌型丙酮酸激酶 M2 通过激活整合素 β1/FAK 信号通路促进肺癌转移。

Secreted Pyruvate Kinase M2 Promotes Lung Cancer Metastasis through Activating the Integrin Beta1/FAK Signaling Pathway.

机构信息

Cancer Biology Laboratory, School of Life Sciences, Tsinghua University, Beijing 100084, China; The National Engineering Laboratory for Anti-Tumor Protein Therapeutics, Tsinghua University, Beijing 100084, China; Beijing Key Laboratory for Protein Therapeutics, Tsinghua University, Beijing 100084, China.

Cancer Biology Laboratory, School of Life Sciences, Tsinghua University, Beijing 100084, China; The National Engineering Laboratory for Anti-Tumor Protein Therapeutics, Tsinghua University, Beijing 100084, China; Beijing Key Laboratory for Protein Therapeutics, Tsinghua University, Beijing 100084, China.

出版信息

Cell Rep. 2020 Feb 11;30(6):1780-1797.e6. doi: 10.1016/j.celrep.2020.01.037.

Abstract

Cancer cell-derived secretomes have been documented to play critical roles in cancer progression. Intriguingly, alternative extracellular roles of intracellular proteins are involved in various steps of tumor progression, which can offer strategies to fight cancer. Herein, we identify lung cancer progression-associated secretome signatures using mass spectrometry analysis. Among them, PKM2 is verified to be highly expressed and secreted in lung cancer cells and clinical samples. Functional analyses demonstrates that secreted PKM2 facilitates tumor metastasis. Furthermore, mass spectrometry analysis and functional validation identify integrin β1 as a receptor of secreted PKM2. Mechanistically, secreted PKM2 directly bound to integrin β1 and subsequently activated the FAK/SRC/ERK axis to promote tumor metastasis. Collectively, our findings suggest that PKM2 is a potential serum biomarker for diagnosing lung cancer and that targeting the secreted PKM2-integrin β1 axis can inhibit lung cancer development, which provides evidence of a potential therapeutic strategy in lung cancer.

摘要

癌细胞来源的分泌组已被证明在癌症进展中发挥关键作用。有趣的是,细胞内蛋白的替代细胞外作用参与了肿瘤进展的各个步骤,这为对抗癌症提供了策略。在此,我们使用质谱分析鉴定了与肺癌进展相关的分泌组特征。其中,PKM2 在肺癌细胞和临床样本中被证实高度表达和分泌。功能分析表明,分泌的 PKM2 促进肿瘤转移。此外,质谱分析和功能验证鉴定出整合素 β1 是分泌的 PKM2 的受体。在机制上,分泌的 PKM2 直接与整合素 β1 结合,随后激活 FAK/SRC/ERK 轴促进肿瘤转移。综上所述,我们的研究结果表明,PKM2 是诊断肺癌的潜在血清生物标志物,靶向分泌的 PKM2-整合素 β1 轴可以抑制肺癌的发展,为肺癌的潜在治疗策略提供了证据。

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