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癌症相关成纤维细胞诱导癌细胞非依赖金属蛋白酶侵袭基底膜。

Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane.

作者信息

Glentis Alexandros, Oertle Philipp, Mariani Pascale, Chikina Aleksandra, El Marjou Fatima, Attieh Youmna, Zaccarini Francois, Lae Marick, Loew Damarys, Dingli Florent, Sirven Philemon, Schoumacher Marie, Gurchenkov Basile G, Plodinec Marija, Vignjevic Danijela Matic

机构信息

Institut Curie, PSL Research University, CNRS, UMR 144, F-75005, Paris, France.

Biozentrum, University of Basel, CH-4056, Basel, Switzerland.

出版信息

Nat Commun. 2017 Oct 13;8(1):924. doi: 10.1038/s41467-017-00985-8.

DOI:10.1038/s41467-017-00985-8
PMID:29030636
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5640679/
Abstract

At the stage of carcinoma in situ, the basement membrane (BM) segregates tumor cells from the stroma. This barrier must be breached to allow dissemination of the tumor cells to adjacent tissues. Cancer cells can perforate the BM using proteolysis; however, whether stromal cells play a role in this process remains unknown. Here we show that an abundant stromal cell population, cancer-associated fibroblasts (CAFs), promote cancer cell invasion through the BM. CAFs facilitate the breaching of the BM in a matrix metalloproteinase-independent manner. Instead, CAFs pull, stretch, and soften the BM leading to the formation of gaps through which cancer cells can migrate. By exerting contractile forces, CAFs alter the organization and the physical properties of the BM, making it permissive for cancer cell invasion. Blocking the ability of stromal cells to exert mechanical forces on the BM could therefore represent a new therapeutic strategy against aggressive tumors.Stromal cells play various roles in tumor establishment and metastasis. Here the authors, using an ex-vivo model, show that cancer-associated fibroblasts facilitate colon cancer cells invasion in a matrix metalloproteinase-independent manner, likely by pulling and stretching the basement membrane to form gaps.

摘要

在原位癌阶段,基底膜(BM)将肿瘤细胞与基质分隔开来。必须突破这一屏障才能使肿瘤细胞扩散到邻近组织。癌细胞可通过蛋白水解作用穿透基底膜;然而,基质细胞在此过程中是否发挥作用仍不清楚。在此,我们表明一种丰富的基质细胞群体,即癌症相关成纤维细胞(CAFs),可促进癌细胞通过基底膜侵袭。CAFs以一种不依赖基质金属蛋白酶的方式促进基底膜的突破。相反,CAFs牵拉、拉伸并软化基底膜,导致形成癌细胞可迁移通过的间隙。通过施加收缩力,CAFs改变基底膜的组织结构和物理特性,使其有利于癌细胞侵袭。因此,阻断基质细胞对基底膜施加机械力的能力可能代表一种针对侵袭性肿瘤的新治疗策略。基质细胞在肿瘤形成和转移中发挥多种作用。在此,作者利用体外模型表明,癌症相关成纤维细胞以不依赖基质金属蛋白酶的方式促进结肠癌细胞侵袭,可能是通过牵拉和拉伸基底膜以形成间隙。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/4c8c4b693fc4/41467_2017_985_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/e7010a01e8d0/41467_2017_985_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/46d21751ba66/41467_2017_985_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/5dc63371ef80/41467_2017_985_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/407670f10bc7/41467_2017_985_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/4c8c4b693fc4/41467_2017_985_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/e7010a01e8d0/41467_2017_985_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/46d21751ba66/41467_2017_985_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/5dc63371ef80/41467_2017_985_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/407670f10bc7/41467_2017_985_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/5640679/4c8c4b693fc4/41467_2017_985_Fig5_HTML.jpg

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