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癌基因 K2P 钾通道 KCNK9(TASK-3)在卵巢癌中的表达及其预后意义。

Expression and prognostic significance of the oncogenic K2P potassium channel KCNK9 (TASK-3) in ovarian carcinoma.

机构信息

School of Graduate Entry Medicine and Health, University of Nottingham, Uttoxeter Road, Derby, UK.

出版信息

Anticancer Res. 2013 Apr;33(4):1401-8.

PMID:23564779
Abstract

BACKGROUND/AIMS: The TWIK-related acid sensitive K(+) channel-3 (TASK-3) is an oncogenic potassium channel. We investigated the expression of TASK-3 in human ovaries, examined its prognostic significance, and determined effects of TASK-3 blockers on cell proliferation and apoptosis.

MATERIALS AND METHODS

Immunofluorescence and western blotting were used to investigate TASK-3 expression in two ovarian cancer cell lines, normal ovarian surface epithelium and cancer. Immunohistochemistry quantified expression in an ovarian cancer tissue microarray. The effect of TASK-3 blocking agents on cell proliferation was investigated with the CellTiter 96® Aqueous Non-Radioactive Cell Proliferation assay and on apoptosis with flow cytometry.

RESULTS

TASK-3 expression was confirmed by immunofluorescence in the SKOV-3 and OVCAR-3 cell lines, normal ovaries (n=4) and ovarian tumours (n=4) and by western blotting in normal ovaries (n=6) and ovarian tumours (n=22). Immunohistochemistry demonstrated immunostaining in 99% of tumours (n=230). Increased immunostaining conferred a survival advantage (p=0.002; median survival of >24 months). TASK-3 blockers caused a significant reduction in cell proliferation and an increase in apoptosis in the SKOV-3 and OVCAR-3 cell lines.

CONCLUSION

TASK-3 is expressed in epithelial ovarian cancer, conferring a significant survival advantage on patients with increased expression. TASK-3-modulating agents have a significant effect on cell proliferation and apoptosis. Based on these results, we propose that TASK-3 could prove to be both a novel tumour marker and a new therapeutic target in ovarian cancer, but further investigation is required.

摘要

背景/目的:TWIK 相关酸敏感钾通道-3(TASK-3)是一种致癌钾通道。我们研究了 TASK-3 在人卵巢中的表达,检测了其预后意义,并确定了 TASK-3 阻断剂对细胞增殖和凋亡的影响。

材料和方法

使用免疫荧光和 Western blot 检测两种卵巢癌细胞系、正常卵巢表面上皮和癌细胞中 TASK-3 的表达。免疫组织化学方法对卵巢癌组织微阵列中 TASK-3 的表达进行了定量分析。使用 CellTiter 96® Aqueous Non-Radioactive Cell Proliferation assay 检测 TASK-3 阻断剂对细胞增殖的影响,用流式细胞术检测对细胞凋亡的影响。

结果

在 SKOV-3 和 OVCAR-3 细胞系、正常卵巢(n=4)和卵巢肿瘤(n=4)中通过免疫荧光证实了 TASK-3 的表达,在正常卵巢(n=6)和卵巢肿瘤(n=22)中通过 Western blot 也证实了 TASK-3 的表达。免疫组化显示 99%的肿瘤(n=230)存在免疫染色。免疫染色增加与生存优势相关(p=0.002;中位生存期>24 个月)。TASK-3 阻断剂在 SKOV-3 和 OVCAR-3 细胞系中导致细胞增殖显著减少和凋亡增加。

结论

TASK-3 在卵巢上皮性癌中表达,增加表达的患者生存优势显著。TASK-3 调节剂对细胞增殖和凋亡有显著影响。基于这些结果,我们提出 TASK-3 可能成为卵巢癌的新型肿瘤标志物和新的治疗靶点,但需要进一步研究。

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