Wang Wei-Kuang, Chen Man-Chin, Leong Hon-Fai, Kuo Yu-Liang, Kuo Chun-Yu, Lee Che-Hsin
Department of Environmental Engineering and Science, Feng Chia University, Taichung 40407, Taiwan.
Graduate Institute of Basic Medical Science, School of Medicine, China Medical University, Taichung 40404, Taiwan.
Int J Mol Sci. 2014 Dec 26;16(1):439-51. doi: 10.3390/ijms16010439.
Previous work showed that connexin 43 (Cx43) reduced the expression of hypoxic-induced factor-1α (HIF-1α) in astrocytes. HIF-1α is a master transcription factor for angiogenesis in tumor. Angiogenesis is essential for tumor progression. Here, we investigated the role of Cx43 in vascular endothelial growth factor (VEGF) production and angiogenesis in murine tumor. In the study, mouse B16F10 and 4T1 cells were overexpressed or knockdown with Cx43. The expression profiles as well as activity of the treated cells were examined. Furthermore, reduced Cx43 expression in B16F10 and 4T1 cells causes increased expression of VEGF and enhanced the proliferation of endothelial cells. On the contrary, the expression of VEGF and the proliferation of endothelial were increased in the conditioned medium of Cx43-knockdown tumor cells. We subcutaneously transplanted Cx43-overexpressing B16F10 cells into mice to evaluate the roles of Cx43 in the tumor angiogenesis. Both tumor size and the number of vessels growing in the tumor were markedly decreased compare with control group. Our findings suggest that Cx43 inhibited tumor growth by reducing angiogenesis.
先前的研究表明,连接蛋白43(Cx43)可降低星形胶质细胞中缺氧诱导因子-1α(HIF-1α)的表达。HIF-1α是肿瘤血管生成的主要转录因子。血管生成对肿瘤进展至关重要。在此,我们研究了Cx43在小鼠肿瘤中血管内皮生长因子(VEGF)产生及血管生成中的作用。在该研究中,小鼠B16F10和4T1细胞被过表达或敲低Cx43。检测了处理后细胞的表达谱及活性。此外,B16F10和4T1细胞中Cx43表达降低导致VEGF表达增加,并增强了内皮细胞的增殖。相反,在Cx43敲低肿瘤细胞的条件培养基中,VEGF的表达及内皮细胞的增殖增加。我们将过表达Cx43的B16F10细胞皮下移植到小鼠体内,以评估Cx43在肿瘤血管生成中的作用。与对照组相比,肿瘤大小及肿瘤内生长的血管数量均显著减少。我们的研究结果表明,Cx43通过减少血管生成来抑制肿瘤生长。