Ouabain Promotes Gap Junctional Intercellular Communication in Cancer Cells

被引:4
作者
Serrano-Rubi, Mauricio [1 ]
Jimenez, Lidia [1 ]
Martinez-Rendon, Jacqueline [1 ]
Cereijido, Marcelino [1 ]
Ponce, Arturo [1 ]
机构
[1] CINVESTAV IPN, Dept Physiol Biophys & Neurosci, Mexico City 07360, DF, Mexico
关键词
gap junctions; ouabain; cancer; CONNEXIN GENES; E-CADHERIN; INCREASED SUSCEPTIBILITY; KINASE INHIBITOR; DOWN-REGULATION; TISSUE-GROWTH; HUMAN BREAST; RHO-GTPASES; OLD ENZYME; IN-VITRO;
D O I
10.3390/ijms22010358
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gap junctions are molecular structures that allow communication between neighboring cells. It has been shown that gap junctional intercellular communication (GJIC) is notoriously reduced in cancer cells compared to their normal counterparts. Ouabain, a plant derived substance, widely known for its therapeutic properties on the heart, has been shown to play a role in several types of cancer, although its mechanism of action is not yet fully understood. Since we have previously shown that ouabain enhances GJIC in epithelial cells (MDCK), here we probed whether ouabain affects GJIC in a variety of cancer cell lines, including cervico-uterine (CasKi, SiHa and Hela), breast (MDA-MB-321 and MCF7), lung (A549), colon (SW480) and pancreas (HPAF-II). For this purpose, we conducted dye transfer assays to measure and compare GJIC in monolayers of cells with and without treatment with ouabain (0.1, 1, 10, 50 and 500 nM). We found that ouabain induces a statistically significant enhancement of GJIC in all of these cancer cell lines, albeit with distinct sensitivity. Additionally, we show that synthesis of new nucleotides or protein subunits is not required, and that Csrc, ErK1/2 and ROCK-Rho mediate the signaling mechanisms. These results may contribute to explaining how ouabain influences cancer.
引用
收藏
页码:1 / 18
页数:18
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