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糖基磷脂酰肌醇特异性磷脂酶 D 促进肿瘤转移的机制研究

Asialoglycoprotein receptor promotes cancer metastasis by activating the EGFR-ERK pathway.

机构信息

Laboratory of Cancer Biology and Molecular Immunology, Graduate School of Pharmaceutical Sciences, University of Tokyo, Bunkyo-ku, Japan.

出版信息

Cancer Res. 2011 Oct 15;71(20):6419-27. doi: 10.1158/0008-5472.CAN-11-1773. Epub 2011 Aug 25.

Abstract

Although the importance of glycans in malignant cell behavior is well documented, the potential involvement of endogenous lectins as modifiers of progression and metastasis in the tumor microenvironment has not been explored. In this study, we show that loss of the hepatic asialoglycoprotein receptor (ASGPR) in mice severely reduces the frequency of spontaneous lung metastasis after intrahepatic implantation of murine Lewis lung carcinoma (3LL) cells. Conversely, in vitro treatment with recombinant ASGPR increased the invasive and metastatic capacity of 3LL cells before intrahepatic implantation. ASGPR treatment in vitro increased the expression and production of matrix metalloproteinase-9 through activation of the epidermal growth factor receptor-extracellular signal-regulated kinase (EGFR-ERK) pathway. Our findings identify ASGPR as a novel important factor that responds to endogenous lectins in the tumor microenvironment to promote cancer metastasis by activating the EGFR-ERK pathway through interactions with counter-receptors on cancer cells.

摘要

尽管糖蛋白在恶性细胞行为中的重要性已得到充分证明,但内源性凝集素作为肿瘤微环境中进展和转移的调节剂的潜在作用尚未得到探索。在这项研究中,我们表明,小鼠肝脏去唾液酸糖蛋白受体(ASGPR)的缺失严重降低了肝内植入小鼠 Lewis 肺癌(3LL)细胞后自发性肺转移的频率。相反,体外用重组 ASGPR 处理可增加 3LL 细胞在肝内植入前的侵袭和转移能力。ASGPR 体外处理通过激活表皮生长因子受体-细胞外信号调节激酶(EGFR-ERK)途径增加基质金属蛋白酶-9 的表达和产生。我们的发现确定 ASGPR 是一种新的重要因子,它通过与癌细胞上的对应受体相互作用,响应肿瘤微环境中的内源性凝集素,通过激活 EGFR-ERK 途径促进癌症转移。

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