Department of Cell Biology, University of Calabria, Via P. Bucci 4c 87036 Arcavacata di Rende, Italy.
Cell Biochem Funct. 2012 Jul;30(5):419-25. doi: 10.1002/cbf.2816. Epub 2012 Feb 28.
The expression of carnitine plasma membrane transporter OCTN2 was evaluated in virus and nonvirus-mediated cancer. Both OCTN2 mRNA and protein levels were reduced in keratinocytes retrotransduced with HPV16 E6 and E7 compared with the control. The OCTN2 expression was reduced also in keratinocytes retrotransduced with the sole HPV16 E6. A similar down-regulation of OCTN2 mRNA level was observed in a naturally HPV16-infected cancer cell line, CaSki, harbouring several copies of HPV16 whole genome. The mechanism of down-regulation is not related to p53 transcriptional activity because in SAOS (p53-null) cell line, the restoration of p53 expression did not rescue OCTN2 expression. The treatment of keratinocytes retrotransduced with HPV16 E6 and E7 with 5-aza-cytidine rescued the OCTN2 expression, indicating that the mechanism of down-regulation is linked to DNA methylation. Low levels of mRNA expression of OCTN2 were found also in several nonvirus-related epithelial cancer cell lines. The treatment of those cell lines with 5-aza-cytidine again rescued the expression of OCTN2 as well. These data demonstrate for the first time that the OCTN2 transporter is generally down-regulated in virus and nonvirus-mediated epithelial cancers, probably via methylation of its promoter region.
OCTN2 蛋白表达在病毒和非病毒介导的癌症中均被下调。与对照组相比,HPV16 E6 和 E7 逆转录的角化细胞中 OCTN2 mRNA 和蛋白水平均降低。仅 HPV16 E6 逆转录的角化细胞中 OCTN2 表达也降低。在含有 HPV16 全基因组多个拷贝的天然 HPV16 感染的宫颈癌细胞系 CaSki 中,观察到 OCTN2 mRNA 水平的类似下调。下调的机制与 p53 转录活性无关,因为在 SAOS(p53 缺失)细胞系中,p53 表达的恢复不能挽救 OCTN2 的表达。用 5-氮杂胞苷处理 HPV16 E6 和 E7 逆转录的角化细胞可挽救 OCTN2 的表达,表明下调的机制与 DNA 甲基化有关。在几种非病毒相关的上皮癌细胞系中也发现 OCTN2 的 mRNA 表达水平较低。再次用 5-氮杂胞苷处理这些细胞系可挽救 OCTN2 的表达。这些数据首次表明,OCTN2 转运蛋白在病毒和非病毒介导的上皮癌中普遍下调,可能是通过其启动子区域的甲基化。