Up-regulation of Kv7.1 channels in thromboxane A^sub 2^-induced colonic cancer cell proliferation

Thromboxane A^sub 2^ (TXA^sub 2^) is known to stimulate colonic cancer cell proliferation, although the mechanism has not been clarified. In this study, we compared the expression levels of Kv7.1 K^sup +^ channels between human colorectal cancer tissue and the accompanying non-tumor mucosa. Kv7.1 pr...

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Veröffentlicht in:Pflügers Archiv 2014-03, Vol.466 (3), p.541
Hauptverfasser: Shimizu, Takahiro, Fujii, Takuto, Takahashi, Yuji, Takahashi, Yuta, Suzuki, Tomoyuki, Ukai, Masashi, Tauchi, Katsunori, Horikawa, Naoki, Tsukada, Kazuhiro, Sakai, Hideki
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Sprache:eng
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Zusammenfassung:Thromboxane A^sub 2^ (TXA^sub 2^) is known to stimulate colonic cancer cell proliferation, although the mechanism has not been clarified. In this study, we compared the expression levels of Kv7.1 K^sup +^ channels between human colorectal cancer tissue and the accompanying non-tumor mucosa. Kv7.1 proteins were found to be consistently up-regulated in the cancer tissues from different patients. Kv7.1 was also expressed in human colonic cancer cell lines. Treatment of colonic cancer cells with 9,11-epithio-11,12-methano-thromboxane A^sub 2^ (STA^sub 2^), a stable analogue of TXA^sub 2^, significantly increased whole-cell K^sup +^ currents sensitive to chromanol 293B, an inhibitor of Kv7.1 channels, in parallel with an increased expression of Kv7.1 proteins. In contrast, TXB^sub 2^, an inactive metabolite of TXA^sub 2^, had no effects on expression level and function of Kv7.1. A TXA^sub 2^ receptor antagonist (SQ29548) and an inhibitor of cAMP-dependent protein kinase (Rp-8-Br-MB-cAMPS) inhibited STA^sub 2^-induced increases in both Kv7.1 expression and chromanol 293B-sensitive K^sup +^ currents. Interestingly, STA^sub 2^-stimulated proliferation of colonic cancer cells was inhibited by chromanol 293B. These results suggest that Kv7.1 channels are involved in the TXA^sub 2^-induced cancer cell proliferation and that they are up-regulated by the TXA^sub 2^ receptor-mediated cAMP pathway.[PUBLICATION ABSTRACT]
ISSN:0031-6768
1432-2013
DOI:10.1007/s00424-013-1341-x