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A disintegrin and metalloproteinase 8 induced epithelial‐mesenchymal transition to promote the invasion of colon cancer cells via TGF‐β/Smad2/3 signalling pathway

机译:解毒素和金属蛋白酶8诱导上皮 - 间充质转变以通过TGF-β/ SMAD2 / 3信号通路促进结肠癌细胞的侵袭

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摘要

A disintegrin and metalloproteinase 8 (ADAM8) protein is a multi‐domain transmembrane glycoprotein which involves in extracellular matrix remodelling, cell adhesion, invasion and migration. ADAM8 and epithelial‐mesenchymal transition (EMT) play an important role in tumour invasion has been well established. However, the interaction between ADAM8 and EMT has remained unclear. The data of colon cancer patients obtained from TCGA (The Cancer Genome Atlas) and GTEx (Genotype‐Tissue Expression Project) were analysed by the bioinformatics research method. The expression of ADAM8 in colon cancer cells was up‐regulated and down‐regulated by transfecting with the expression plasmid and small interfering RNA, respectively. Transwell invasion assay, immunohistochemistry, immunocytochemistry, Western blotting and qRT‐PCR were utilized to study the effect of ADAM8 on colon cancer cell's EMT and its related mechanisms. Analysis of TCGA and GTEx data revealed that ADAM8 was linked to poor overall survival in colon cancer patients. Besides, ADAM8 was correlated with multiple EMT biomarkers (E‐cadherin, N‐cadherin, Vimentin, Snail2 and ZEB2). In vitro, we also proved that the up‐regulation of ADAM8 could promote EMT effect and enhance the invasive ability of colon cancer cells. On the contrary, the down‐regulation of ADAM8 in colon cancer cells attenuated these effects above. Further studies suggested that ADAM8 modulated EMT on colon cancer cells through TGF‐β/Smad2/3 signalling pathway. Our research suggested that ADAM8 could be a potential biomarker for the prognosis of colon cancer and induced EMT to promote the invasion of colon cancer cells via activating TGF‐β/Smad2/3 signalling pathway.
机译:解毒素和金属蛋白酶8(ADAM8)蛋白是一种多域跨膜糖蛋白,其涉及细胞外基质重塑,细胞粘附,侵袭和迁移。 ADAM8和上皮 - 间充质转换(EMT)在肿瘤侵袭中发挥着重要作用。然而,ADAM8和EMT之间的相互作用仍然不清楚。通过生物信息学研究方法分析从TCGA(癌症基因组Atlas)和GTEX(基因型组织表达项目)获得的结肠癌患者的数据。通过分别用表达质粒和小干扰RNA转染结肠癌细胞中的ADAM8在结肠癌细胞中的表达。用于研究ADAM8对结肠癌细胞EMT及其相关机制的影响,利用Trouswerverventry,免疫组化,免疫细胞化学,免疫印迹和QRT-PCR。 TCGA和GTEX数据分析显示,Adam8与结肠癌患者的整体生存率有关。此外,Adam8与多个EMT生物标志物(E-Cadherin,N-Cadherin,Vimentin,Snail2和Zeb2)相关。体外,我们还证明了Adam8的上调可以促进EMT效应并提高结肠癌细胞的侵袭能力。相反,结肠癌细胞的Adam8的下调衰减了上述效果。进一步的研究表明,Adam8通过TGF-β/ Smad2 / 3信号通路调节结肠癌细胞的EMT。我们的研究表明,Adam8可以是结肠癌预后的潜在生物标志物,并诱导EMT通过激活TGF-β/ Smad2 / 3信号通路促进结肠癌细胞的侵袭。

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