WM Keck Center for Transgene Research, University of Notre Dame, Notre Dame, Indiana, United States of America.
PLoS One. 2011;6(10):e25725. doi: 10.1371/journal.pone.0025725. Epub 2011 Oct 3.
Matrix metalloproteinase 7 (MMP7), a metallohydrolase involved in the development of several cancers, is downregulated in the Apc(Min/+) colon cancer mouse model following sulindac treatment. To determine whether this effect is relevant to the human condition, HT-29 human colon cancer cells were treated with sulindac and its metabolites, and compared to results obtained from in vivo mouse studies. The expression of MMP7 was monitored. The results demonstrated that sulindac sulfide effectively downregulated both MMP7 expression and activity. Furthermore, activity-based proteomics demonstrated that sulindac sulfide dramatically decreased the activity of leukotriene A4 hydrolase in HT-29 cells as reflected by a decrease in the level of its product, leukotriene B4. This study demonstrates that the effect of sulindac treatment in a mouse model of colon cancer may be relevant to the human counterpart and highlights the effect of sulindac treatment on metallohydrolases.
基质金属蛋白酶 7(MMP7)是一种参与多种癌症发展的金属水解酶,在 APC(Min/+)结肠癌小鼠模型中,在用舒林酸治疗后其表达下调。为了确定这种作用是否与人类状况相关,用舒林酸及其代谢物处理 HT-29 人结肠癌细胞,并与体内小鼠研究的结果进行比较。监测 MMP7 的表达。结果表明,舒林酸亚砜能有效下调 MMP7 的表达和活性。此外,基于活性的蛋白质组学研究表明,舒林酸亚砜显著降低了 HT-29 细胞中白三烯 A4 水解酶的活性,反映在其产物白三烯 B4 的水平下降。本研究表明,舒林酸治疗结肠癌小鼠模型的效果可能与人类相对应,并强调了舒林酸治疗对金属水解酶的作用。