TFPI-2 silencing increases tumour progression and promotes metalloproteinase 1 and 3 induction through tumour-stromal cell interactions

间质细胞 细胞外基质 癌症研究 基因沉默 基质金属蛋白酶 癌细胞 生物 小干扰RNA 层粘连蛋白 基底膜 转移 细胞迁移 细胞 癌症 病理 细胞培养 细胞生物学 医学 转染 生物化学 遗传学 基因
作者
Guillaume Gaud,Sophie Iochmann,Audrey Guillon‐Munos,B. Brillet,S. Petiot,Florian Seigneuret,Antoine Touzé,Nathalie Heuzé-Vourc’h,Yves Courty,Stéphanie Lerondel,Yves Gruel,Pascale Reverdiau
出处
期刊:Journal of Cellular and Molecular Medicine [Wiley]
卷期号:15 (2): 196-208 被引量:27
标识
DOI:10.1111/j.1582-4934.2009.00989.x
摘要

Tissue factor pathway inhibitor-2 (TFPI-2) is a potent inhibitor of plasmin which activates matrix metalloproteinases (MMPs) involved in degradation of the extracellular matrix. Its secretion in the tumour microenvironment makes TFPI-2 a potential inhibitor of tumour invasion and metastasis. As demonstrated in aggressive cancers, TFPI-2 is frequently down-regulated in cancer cells, but the mechanisms involved in the inhibition of tumour progression remained unclear. We showed in this study that stable TFPI-2 down-regulation in the National Cancer Institute (NCI)-H460 non-small cell lung cancer cell line using specific micro interfering micro-interfering RNA promoted tumour progression in a nude mice orthotopic model that resulted in an increase in cell invasion. Moreover, TFPI-2 down-regulation enhanced cell adhesion to collagen IV and laminin via an increase in α(1) integrin on cell surface, and increased MMP expression (mainly MMP-1 and -3) contributing to cancer cell invasion through basement membrane components. This study also reveals for the first time that pulmonary fibroblasts incubated with conditioned media from TFPI-2 silencing cancer cells exhibited increased expression of MMPs, particularly MMP-1, -3 and -7, that are likely involved in lung cancer cell invasion through the surrounding stromal tissue, thus enhancing formation of metastases.
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