Suppr超能文献

一种广泛表达的独特 Vκ4-1/Jκ3 模式的游离免疫球蛋白 κ 链通过激活整合素 β1/FAK 通路促进结肠癌的侵袭和转移。

A widely expressed free immunoglobulin κ chain with a unique Vκ4-1/Jκ3 pattern promotes colon cancer invasion and metastasis by activating the integrin β1/FAK pathway.

机构信息

Department of Immunology, Peking University Health Science Center, Beijing, 100191, China; Key Laboratory of Medical Immunology, Ministry of Health, Beijing, 100191, China.

Department of Immunology, Southern Medical University, Guangzhou, 510515, China; Clinical Laboratory, Guangzhou Women and Children Hospital, Guangzhou, 510000, China.

出版信息

Cancer Lett. 2022 Aug 1;540:215720. doi: 10.1016/j.canlet.2022.215720. Epub 2022 May 7.

Abstract

Historically, immunoglobulin (Ig) has been known as an antibody and is expressed only in B lineage cells; importantly, Ig light chains are conjugated to heavy chains to form intact Igs. However, in this study, we found a free Igκ light chain with a unique Vκ4-1/Jκ3 rearrangement (Vκ4-1/Jκ3-FLC) that was widely expressed in different non-B lineages and was overexpressed in cancer cells. Further study indicated that Vκ4-1/Jκ3-FLC was hydrophobic, formed obvious insoluble deposits in the extracellular matrix (ECM) and existed in free form. Functional analyses demonstrated that Vκ4-1/Jκ3-FLC promoted the proliferation, migration and metastasis of colon cancer cells in vitro and in vivo. Mechanistically, Vκ4-1/Jκ3-FLC bound to integrin β1 and activated the FAK and Src pathways. More importantly, specific antibodies against the variable region of Vκ4-1/Jκ3-FLC significantly inhibited the growth of colon cancer tumors. Our findings suggested that Vκ4-1/Jκ3-FLC is a novel ECM protein and integrin β1 ligand and that it is involved in cancer progression and is a potential therapeutic target in cancer, particularly colon cancer.

摘要

从历史上看,免疫球蛋白(Ig)被认为是抗体,仅在 B 细胞谱系中表达;重要的是,Ig 轻链与重链结合形成完整的 Ig。然而,在这项研究中,我们发现了一种广泛表达于不同非 B 细胞谱系且在癌细胞中过表达的独特 Vκ4-1/Jκ3 重排的游离 Igκ轻链(Vκ4-1/Jκ3-FLC)。进一步的研究表明,Vκ4-1/Jκ3-FLC 具有疏水性,在细胞外基质(ECM)中形成明显的不溶性沉积物,并以游离形式存在。功能分析表明,Vκ4-1/Jκ3-FLC 促进了结肠癌在体外和体内的增殖、迁移和转移。在机制上,Vκ4-1/Jκ3-FLC 与整合素 β1 结合并激活 FAK 和 Src 途径。更重要的是,针对 Vκ4-1/Jκ3-FLC 可变区的特异性抗体显著抑制了结肠癌肿瘤的生长。我们的研究结果表明,Vκ4-1/Jκ3-FLC 是一种新型 ECM 蛋白和整合素 β1 配体,它参与癌症的进展,是癌症,特别是结肠癌的潜在治疗靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验