Fujimoto Eriko, Satoh Haruna, Negishi Etsuko, Ueno Koichi, Nagashima Yoji, Hagiwara Kiyokazu, Yamasaki Hiroshi, Yano Tomohiro
Faculty of Pharmaceutical Sciences, Chiba University, Chiba, Japan.
Mol Carcinog. 2004 Jul;40(3):135-42. doi: 10.1002/mc.20025.
Connexin (Cx) genes have negative growth effects on tumor cells with certain cell specificity. We have previously reported that Cx32 is specifically downregulated in human renal cell carcinoma cell (RCC) lines as well as cancerous regions of kidneys and that the Cx is expressed in the progenitor cells of the carcinoma. However, the precise role of Cx32 in growth control of RCC cells remains unknown. In this study, we examined whether Cx32 could act in growth control against a human RCC cell, Caki-2 cell. In order to estimate the cell growth control, we established Caki-2 cells that have stable expression of Cx32 genes. Cx32 expression in Caki-2 cells induced contact inhibition of growth and reduced anchorage-independent growth ability, but did not significantly affect lag phase growth rates. This growth control by Cx32 was dependent on the inhibition of the cell-cycle transition from G1 to S phase at high cell density, and the inhibition of the cell-cycle transition related to the suppression of Her-2 activation. Furthermore, the suppression of Cx32 expression in Caki-2 cells by short interfering RNA induced the activation of Her-2. These data suggest that Cx32 has negative growth control of Caki-2 cells, partly due to the inhibition of the Her-2 activation.
连接蛋白(Cx)基因对肿瘤细胞具有负向生长作用,且具有一定的细胞特异性。我们之前报道过,Cx32在人肾癌细胞(RCC)系以及肾脏癌组织区域中特异性下调,并且该连接蛋白在癌祖细胞中表达。然而,Cx32在RCC细胞生长调控中的精确作用仍不清楚。在本研究中,我们检测了Cx32是否能对人RCC细胞Caki-2细胞发挥生长调控作用。为了评估细胞生长调控情况,我们建立了稳定表达Cx32基因的Caki-2细胞。Caki-2细胞中Cx32的表达诱导了生长的接触抑制并降低了非锚定依赖性生长能力,但对延迟期生长速率没有显著影响。Cx32的这种生长调控依赖于在高细胞密度下对细胞周期从G1期到S期转变的抑制,以及与抑制Her-2激活相关的细胞周期转变的抑制。此外,通过短发夹RNA抑制Caki-2细胞中Cx32的表达会诱导Her-2的激活。这些数据表明,Cx32对Caki-2细胞具有负向生长调控作用,部分原因是对Her-2激活的抑制。