Gao Jinhang, Wen Shilei, Zhou Hongying, Feng Shi
Department of Human Anatomy, Academy of Preclinical and Forensic Medicine, West China Medicine College, Sichuan University, Chengdu, Sichuan 610041, P.R. China.
Mol Med Rep. 2015 Nov;12(5):7033-8. doi: 10.3892/mmr.2015.4256. Epub 2015 Aug 26.
DNA methylation occurs in the displacement loop (D-loop) region of mammals; however, D-loop regions of certain tumor tissue types were found to be de‑methylated. Whether hypomethylation of the D‑loop region is involved in the regulation of the mitochondrial DNA (mtDNA) copy number and nicotinamide adenine dinucleotide subunit 2 (ND‑2) expressions in colorectal cancer has remained elusive. In the present study, the association between methylation status of the D‑loop region, mtDNA copy number and ND‑2 expression was investigated in 65 colorectal cancer specimens and their corresponding non‑cancerous tissues. In addition, a de‑methylation experiment was performed on the Caco‑2 colorectal cancer cell line by using 5‑aza-2'-deoxycytidine (5‑Aza). The methylation rate of the D‑loop region in all 65 colorectal cancer tissues was markedly reduced when compared with that of their corresponding non‑cancerous tissues (13.8 vs. 81.5%; P<0.05). Furthermore, the methylation rate of the D‑loop region in colorectal cancer tissues was markedly decreased in clinicopathological stages III and IV compared with that in clinicopathological stages I and II (7.1 and 0% vs. 25 and 16%; P<0.05). In addition, the mean relative mtDNA copy number and ND‑2 expression in colorectal cancer tissues were increased compared with those in the corresponding non‑cancerous tissues. De‑methylation of the D‑loop region was associated with an elevated mtDNA copy number and an increased ND‑2 expression. Furthermore, the mtDNA copy number and ND‑2 expression in Caco‑2 cells were significantly increased after 5‑Aza treatment. In conclusion, de‑methylation of the D‑loop region is likely to be involved in the regulation of the mtDNA copy number and ND-2 expression.
DNA甲基化发生在哺乳动物的置换环(D环)区域;然而,发现某些肿瘤组织类型的D环区域发生了去甲基化。D环区域的低甲基化是否参与结直肠癌中线粒体DNA(mtDNA)拷贝数和烟酰胺腺嘌呤二核苷酸亚基2(ND-2)表达的调控仍不清楚。在本研究中,在65例结直肠癌标本及其相应的癌旁组织中研究了D环区域甲基化状态、mtDNA拷贝数与ND-2表达之间的关联。此外,通过使用5-氮杂-2'-脱氧胞苷(5-Aza)对Caco-2结直肠癌细胞系进行了去甲基化实验。与相应的癌旁组织相比,所有65例结直肠癌组织中D环区域的甲基化率均显著降低(13.8%对81.5%;P<0.05)。此外,与临床病理分期I和II相比,临床病理分期III和IV的结直肠癌组织中D环区域的甲基化率显著降低(7.1%和0%对25%和16%;P<0.05)。此外,结直肠癌组织中的平均相对mtDNA拷贝数和ND-2表达高于相应的癌旁组织。D环区域的去甲基化与mtDNA拷贝数升高和ND-2表达增加相关。此外,5-Aza处理后Caco-2细胞中的mtDNA拷贝数和ND-2表达显著增加。总之,D环区域的去甲基化可能参与mtDNA拷贝数和ND-2表达的调控。