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高迁移率族蛋白B1通过Toll样受体4/核因子κB信号通路激活整合素αvβ3/黏着斑激酶,从而诱导人非小细胞肺癌细胞迁移。

HMGB1 induces human non-small cell lung cancer cell motility by activating integrin αvβ3/FAK through TLR4/NF-κB signaling pathway.

作者信息

Zhu Jianhua, Luo Jing, Li Yongchao, Jia Min, Wang Yueqin, Huang Yan, Ke Shuhong

机构信息

Laboratory of Clinical Immunology, Wuhan No. 1 Hospital, Tongji Medical College, Huazhong University of Science and Technology (HUST), Wuhan, Hubei, PR China.

Department of Immunology, Tongji Medical College, Huazhong University of Science and Technology (HUST), Wuhan, Hubei, PR China.

出版信息

Biochem Biophys Res Commun. 2016 Nov 25;480(4):522-527. doi: 10.1016/j.bbrc.2016.10.052. Epub 2016 Oct 18.

Abstract

High mobility group box 1 (HMGB1) is a ubiquitous nuclear protein with multi-functions and plays an important role in tumorigenesis and metastasis in various human cancers. In the present study, we found that HMGB1 induced migration of in human non-small cell lung cancer (NSCLC) cells by up-regulating integrin αvβ3 expression. Further investigation evidenced that HMGB1 activated Toll-like receptor 4 (TLR4) and NF-κB, which was responsible for αvβ3 up-regulation. Furthermore, HMGB1-induced integrin αvβ3 expression led to focal adhesion kinase (FAK) phosphorylation and increased paxillin and talin mRNA expression. Knockdown HMGB1 inhibited xenograft tumor metastasis in athymic mice. Taken together, our findings suggested that HMGB1 enhances tumor cell migration ability by activating αvβ3/FAK through TLR4/NF-κB signaling, leading to metastasis of NSCLC.

摘要

高迁移率族蛋白B1(HMGB1)是一种普遍存在的多功能核蛋白,在多种人类癌症的肿瘤发生和转移中起重要作用。在本研究中,我们发现HMGB1通过上调整合素αvβ3的表达诱导人非小细胞肺癌(NSCLC)细胞迁移。进一步研究证明,HMGB1激活了Toll样受体4(TLR4)和核因子κB(NF-κB),这是αvβ3上调的原因。此外,HMGB1诱导的整合素αvβ3表达导致粘着斑激酶(FAK)磷酸化,并增加桩蛋白和踝蛋白的mRNA表达。敲低HMGB1可抑制无胸腺小鼠的异种移植肿瘤转移。综上所述,我们的研究结果表明,HMGB1通过TLR4/NF-κB信号通路激活αvβ3/FAK,增强肿瘤细胞迁移能力,导致NSCLC转移。

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