基质金属蛋白酶
MMP9公司
MMP2型
化学
细胞外基质
转化生长因子
佛波
活性氧
癌症研究
癌细胞
细胞培养
生物化学
细胞凋亡
细胞生物学
生物
酶
癌症
蛋白激酶C
下调和上调
基因
遗传学
作者
Tetsuro Kamiya,Miho Tanaka,Hirokazu Hara,Eiji Yamaguchi,Akichika Itoh,Tetsuo Adachi
标识
DOI:10.1080/10715762.2019.1675874
摘要
Matrix metalloproteinases (MMPs), zinc-containing proteinases, play a critical role in tumour progression by degrading extracellular matrix components. MMP2 and MMP9 are secreted from tumour-associated macrophages as well as tumour cells and have been implicated in the formation of the tumour microenvironment. Therefore, the inhibition of these MMPs may suppress tumour progression and metastasis. 4-Hydroperoxy-2-decenoic acid ethyl ester (HPO-DAEE) is known to cause apoptosis in the human lung cancer cell line A549 by inducing endoplasmic reticulum (ER) stress. However, the effects of HPO-DAEE on tumour progression remain unclear. HPO-DAEE pre-treatment significantly suppressed phorbol 12-myristate 13-acetate (TPA)-triggered MMP activation in human monocytic THP-1 cells. It also enhanced the expression of haem oxygenase-1, an antioxidant enzyme, and suppressed the TPA-triggered intracellular accumulation of reactive oxygen species (ROS). Furthermore, HPO-DAEE suppressed transforming growth factor-β1-triggered human prostate cancer PC3 cell migration and this was accompanied by the inhibition of MMP expression and activities. The present results indicate that HPO-DAEE may exert inhibitory effects on tumour progression by suppressing MMP expression and activities.
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