转移
巴基斯坦卢比
肺癌
癌症研究
癌症
整合素
肿瘤进展
信号转导
细胞生物学
癌细胞
生物
医学
受体
丙酮酸激酶
病理
生物化学
糖酵解
酶
遗传学
作者
Caihong Wang,Shaosen Zhang,Jie Liu,Yang Tian,Boyuan Ma,Siran Xu,Yan Fu,Yongzhang Luo
出处
期刊:Cell Reports
[Elsevier]
日期:2020-02-01
卷期号:30 (6): 1780-1797.e6
被引量:73
标识
DOI:10.1016/j.celrep.2020.01.037
摘要
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.
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