Cai Liqiong, Liu Denghua, Lu Sisi, Xu Yuan, Wang Hongbo
Department of Obstetrics and Gynecology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Uhan, China.
Eur J Gynaecol Oncol. 2014;35(6):625-30.
To investigate the correlation between FOXC2 expression and human cervical cancer, the authors detected FOXC2 expression in cervical cancer cell lines, C33a, SiHa, and Hela. Moreover, FOXC2 expression was measured after TGF-beta1 treatment in C33a cells. Furthermore, the expression level of FOXC2 and microvessel density (MVD) were detected by indirect double-labeled immunofluorescence and laser scanning confocal microscopy in cervix tissue samples, 86 of cervical carcinoma, 54 of cervical intraepithelial neoplasia (CIN), and 30 of normal cervix as controls. The results showed that FOXC2 was expressed in all of the cell lines, and FOXC2 expression in C33a cells can be significantly up-regulated by the treatment of TGF-beta1 and the stimulus was highest when TGF-beta1 is five ng/ml. In cervix tissues, FOXC2 expression gradually increased during the transformation from normal to cancer, and this increase was significantly associated with tumor progression (p < 0.01), lymph node status (p < 0.01), and tumor grade (p < 0.05). FOXC2 expression was positively correlated with MVD (p < 0.05). These results suggest that FOXC2 may promote the development of cervical cancer via regulation of angiogenesis.
为了研究FOXC2表达与人类宫颈癌之间的相关性,作者检测了宫颈癌细胞系C33a、SiHa和Hela中FOXC2的表达。此外,在C33a细胞中用转化生长因子β1(TGF-β1)处理后测量了FOXC2的表达。此外,通过间接双标记免疫荧光和激光扫描共聚焦显微镜检测了86例宫颈癌、54例宫颈上皮内瘤变(CIN)和30例正常宫颈组织样本中FOXC2的表达水平以及微血管密度(MVD)作为对照。结果显示,所有细胞系中均表达FOXC2,TGF-β1处理可使C33a细胞中FOXC2的表达显著上调,当TGF-β1为5 ng/ml时刺激作用最强。在宫颈组织中,从正常到癌症的转变过程中FOXC2表达逐渐增加,且这种增加与肿瘤进展(p<0.01)、淋巴结状态(p<0.01)和肿瘤分级(p<0.05)显著相关。FOXC2表达与MVD呈正相关(p<0.05)。这些结果表明,FOXC2可能通过调节血管生成促进宫颈癌的发展。