基因敲除
基质金属蛋白酶
整合素
细胞生物学
癌症研究
基质(水族馆)
化学
金属蛋白酶
结直肠癌
基质(化学分析)
细胞
生物
细胞培养
癌症
医学
内科学
生物化学
遗传学
色谱法
生态学
作者
Akihiro Nukuda,Chubei Sasaki,Seiichiro Ishihara,Takeomi Mizutani,Kiminori Nakamura,Tokiyoshi Ayabe,K. Kawabata,Hisashi Haga
出处
期刊:Oncogenesis
[Springer Nature]
日期:2015-09-07
卷期号:4 (9): e165-e165
被引量:91
标识
DOI:10.1038/oncsis.2015.24
摘要
Abstract Abnormally stiff substrates have been shown to trigger cancer progression. However, the detailed molecular mechanisms underlying this trigger are not clear. In this study, we cultured T84 human colorectal cancer cells on plastic dishes to create a stiff substrate or on collagen-I gel to create a soft substrate. The stiff substrate enhanced the expression of matrix metalloproteinase-7 (MMP-7), an indicator of poor prognosis. In addition, we used polyacrylamide gels (2, 67 and 126 kPa) so that the MMP-7 expression on the 126-kPa gel was higher compared with that on the 2-kPa gel. Next, we investigated whether yes-associated protein (YAP) affected the MMP-7 expression. YAP knockdown decreased MMP-7 expression. Treatment with inhibitors of epidermal growth factor receptor (EGFR) and myosin regulatory light chain (MRLC) and integrin-α2 or integrin-β1 knockdown downregulated MMP-7 expression. Finally, we demonstrated that YAP, EGFR, integrin-α2β1 and MRLC produced a positive feedback loop that enhanced MMP-7 expression. These findings suggest that stiff substrates enhanced colorectal cancer cell viability by upregulating MMP-7 expression through a positive feedback loop.
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