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口腔鳞状细胞癌中过表达的功能性瞬时受体电位通道 TRPM2。

The overexpressed functional transient receptor potential channel TRPM2 in oral squamous cell carcinoma.

机构信息

Jiangsu Key Laboratory of Oral Diseases and Department of Oral and maxillofacial surgery, Affiliated Hospital of Stomatology, Nanjing Medical University, 136 Hanzhong Road, Nanjing, 210029, China.

Shanghai Key Laboratory of Stomatology and Shanghai Research Institute of Stomatology, Department of Oral and Maxillofacial-Head and Neck Oncology, Ninth People's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200011, China.

出版信息

Sci Rep. 2016 Dec 23;6:38471. doi: 10.1038/srep38471.

Abstract

TRPM2, one member of the transient receptor potential (TRP) protein super-family, is a Ca-permeable channel that is activated by oxidative stress and confers susceptibility to cell death. In the human tongue specimens of carcinoma and the tongue carcinoma SCC cell lines, we observed the enhanced expression of TRPM2. By means of the whole-cell electrophysiological recording, the ADPR-induced currents mediated by TRPM2 were recorded in cultured SCC9 cells. Moreover, after HO treatment for 24 hours, the apoptotic number of SCC9 cells was significantly increased. However, the selectively knocked-down TRPM2 with the small interfering RNA technique inhibited the survival and migration of the SCC9 cancer cells, which was independent of the p53-p21 pathway, since the expression of p21 was enhanced after TRPM2 knockdown. Furthermore, the sub-cellular localization of TRPM2 was remarkably different between cancerous and non-cancerous cells. A significant amount of the TRPM2 proteins were located in the nuclei in cancer cells. All these data suggest that TRPM2 is essential for the survival and migration of SCC cancer cells and may be a potential target for the selective treatment of tongue cancer.

摘要

TRPM2 是瞬时受体电位 (TRP) 蛋白超家族的成员之一,是一种由氧化应激激活的 Ca 通透性通道,易导致细胞死亡。在人类舌癌标本和舌癌细胞 SCC 系中,我们观察到 TRPM2 的表达增强。通过全细胞膜片钳电生理记录,在培养的 SCC9 细胞中记录到由 ADPR 诱导的 TRPM2 介导的电流。此外,HO 处理 24 小时后,SCC9 细胞的凋亡数量显著增加。然而,用小干扰 RNA 技术选择性敲低 TRPM2 抑制了 SCC9 癌细胞的存活和迁移,这与 p53-p21 途径无关,因为在 TRPM2 敲低后 p21 的表达增强。此外,TRPM2 的亚细胞定位在癌细胞和非癌细胞之间有显著差异。大量的 TRPM2 蛋白位于癌细胞的核内。所有这些数据表明,TRPM2 对于 SCC 癌细胞的存活和迁移是必需的,可能是舌癌选择性治疗的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a75/5180100/9a042957c6cf/srep38471-f1.jpg

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