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TSPAN12的上调与结直肠癌的生长和转移相关。

Upregulation of TSPAN12 is associated with the colorectal cancer growth and metastasis.

作者信息

Liu Jiao, Chen Chuang, Li Guang, Chen Dechang, Zhou Qingshan

机构信息

Department of Critical Care Medicine, Renmin Hospital of Wuhan University Wuhan 430060, Hubei Province, China.

Department of Breast and Thyroid Surgery, Renmin Hospital of Wuhan University Wuhan 430060, Hubei Province, China.

出版信息

Am J Transl Res. 2017 Feb 15;9(2):812-822. eCollection 2017.

Abstract

Tetraspanin 12 (TSPAN12), as an earliest member of tetraspanin family, has been recently shown to be highly expressed in several malignant tumors, such as lung cancer and breast cancer, which plays an important role in regulating cell proliferation, migration and invasion. However, the functional roles of TSPAN12 in colorectal cancer (CRC) remain largely unclear. In this study, the expression of TSPAN12 was up-regulated compared to that in paracarcinoma tissues. Higher TSPAN12 expression was significantly correlated with TNM stage, tumor size and lymph node metastasis. The vitro functional analysis, including MTT, colony formation, flow cytometry and transwell assays indicated that lentivirus-mediated TSPAN12 knockdown significantly suppressed cell proliferation, migration and invasion, induced cell apoptosis of CRC cells. In addition, knockdown of TSPAN12 remarkably decreased the growth of subcutaneously inoculated tumors in nude mice. Our findings for the first time supported that TSPAN12 might play a positive role in the regulation of CRC cell proliferation, migration and invasion. The inhibition of TSPAN12 may serve as a novel promising therapeutic strategy against human CRC.

摘要

四跨膜蛋白12(TSPAN12)作为四跨膜蛋白家族的早期成员,最近研究表明其在多种恶性肿瘤中高表达,如肺癌和乳腺癌,在调节细胞增殖、迁移和侵袭中发挥重要作用。然而,TSPAN12在结直肠癌(CRC)中的功能作用仍不清楚。本研究中,与癌旁组织相比,TSPAN12的表达上调。较高的TSPAN12表达与TNM分期、肿瘤大小和淋巴结转移显著相关。体外功能分析,包括MTT、集落形成、流式细胞术和Transwell实验表明,慢病毒介导的TSPAN12敲低显著抑制CRC细胞的增殖、迁移和侵袭,诱导细胞凋亡。此外,TSPAN12敲低显著降低裸鼠皮下接种肿瘤的生长。我们的研究首次证实TSPAN12可能在CRC细胞增殖、迁移和侵袭的调控中起积极作用。抑制TSPAN12可能成为一种有前景的新型抗人CRC治疗策略。

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