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HeLa细胞系中生长控制、肿瘤发生潜能与内源性连接蛋白43表达之间的相关性:对肿瘤进展的影响。

Correlation between growth control, neoplastic potential and endogenous connexin43 expression in HeLa cell lines: implications for tumor progression.

作者信息

King T J, Fukushima L H, Donlon T A, Hieber A D, Shimabukuro K A, Bertram J S

机构信息

Molecular Carcinogenesis, Cancer Research Center of Hawaii, University of Hawaii at Manoa, Honolulu, HI 96813, USA.

出版信息

Carcinogenesis. 2000 Feb;21(2):311-5. doi: 10.1093/carcin/21.2.311.

Abstract

A HeLa cell line, obtained from the ATCC, was cloned and found to exhibit a spectrum of in vitro and in vivo growth characteristics as well as variable expression of endogenous connexin43 (Cx43), a widely expressed gap junction protein implicated in growth control. The majority of clones expressed functional Cx43, which contrasted with previous studies reporting that HeLa cells are completely negative for Cx43 mRNA/protein expression. This endogenous Cx43 expression correlated with increased growth control: Cx43-positive clones exhibited a decreased saturation density and a diminished growth capacity when in co-culture with growth-controlled normal cells in constrast to Cx43-negative clones. Endogenous Cx43 expression was negatively correlated with neoplastic potential as evidenced by attenuated anchorage-independent growth and decreased tumorigenicity in immunodeficient mice. Treatment of Cx43-negative cells with 5-aza-2'-deoxycytidine resulted in expression of Cx43, suggesting gene silencing via DNA methylation. These results support the concept of growth control via junctionally transmitted signals and suggest an epigenetic mechanism for tumor cells to circumvent this control during carcinogenesis. Moreover, the heterogeneous nature of this cell line and the ease of connexin43 gene induction suggest caution in the interpretation of results involving gene transfection using noninducible gene expression systems.

摘要

从美国典型培养物保藏中心(ATCC)获得的一株海拉细胞系被克隆,结果发现它展现出一系列体外和体内生长特性,以及内源性连接蛋白43(Cx43)的可变表达,Cx43是一种广泛表达的间隙连接蛋白,与生长控制有关。大多数克隆表达功能性Cx43,这与之前报道海拉细胞Cx43 mRNA/蛋白表达完全阴性的研究形成对比。这种内源性Cx43表达与生长控制增强相关:与生长受控制的正常细胞共培养时,Cx43阳性克隆的饱和密度降低且生长能力减弱,这与Cx43阴性克隆形成对照。内源性Cx43表达与肿瘤发生潜能呈负相关,这在免疫缺陷小鼠中无锚定依赖性生长减弱和致瘤性降低得到证明。用5-氮杂-2'-脱氧胞苷处理Cx43阴性细胞导致Cx43表达,提示通过DNA甲基化实现基因沉默。这些结果支持通过连接传递信号进行生长控制的概念,并提示肿瘤细胞在致癌过程中规避这种控制的一种表观遗传机制。此外,该细胞系的异质性以及连接蛋白43基因诱导的易感性提示,在解释涉及使用非诱导性基因表达系统进行基因转染的结果时应谨慎。

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