Department of Otolaryngology/Head and Neck Surgery, Hamamatsu University School of Medicine, Shizuoka, Japan.
Cancer Biomark. 2011;10(3-4):135-44. doi: 10.3233/CBM-2012-0242.
Collagen production plays a role in the development of tumors from cancer cells. The aim of the present study is to examine the involvement of epigenetic alteration of Collagen α2 (I) (COL1A2) gene expression in cases of head and neck squamous cell carcinoma (HNSCC).
COL1A2 expression was examined in a panel of cell lines using RT-PCR. The methylation status of the COL1A2 promoter was studied using bisulfate sequencing and methylation-specific PCR (MSP).
COL1A2 expression was absent in 6 of 11 (54.5%) UM-SCC cell lines, whereas three nonmalignant cell lines had stable expressions. MSP analysis showed that 46/98 (46.9%) contained methylated alleles. COL1A2 methylation was significantly correlated with tumor size (P = 0.041), lymph node status (P = 0.008), tumor stage (P = 0.011), H-cadherin methylation (P = 0.039) and disease-free survival (P = 0.005). On multivariate Cox proportional hazard regression, which included age, sex, smoking status, and alcohol exposure, both tumor stage and COL1A2 methylation remained independent prognostic factors.
This study suggests that CpG hypermethylation is a likely mechanism of COL1A2 gene inactivation, supporting the hypothesis that the COL1A2 gene may play a role in the tumorigenesis of HNSCC and may serve as an important biomarker.
胶原蛋白的产生在癌细胞发展为肿瘤的过程中发挥作用。本研究旨在探讨头颈部鳞状细胞癌(HNSCC)中胶原α2(I)(COL1A2)基因表达的表观遗传改变的参与情况。
使用 RT-PCR 检查了一系列细胞系中 COL1A2 的表达情况。使用亚硫酸氢盐测序和甲基化特异性 PCR(MSP)研究 COL1A2 启动子的甲基化状态。
在 11 个 UM-SCC 细胞系中的 6 个(54.5%)中不存在 COL1A2 表达,而 3 个非恶性细胞系具有稳定的表达。MSP 分析显示 46/98(46.9%)包含甲基化等位基因。COL1A2 甲基化与肿瘤大小(P=0.041)、淋巴结状态(P=0.008)、肿瘤分期(P=0.011)、H-钙粘蛋白甲基化(P=0.039)和无病生存时间(P=0.005)显著相关。在包括年龄、性别、吸烟状态和饮酒暴露在内的多变量 Cox 比例风险回归中,肿瘤分期和 COL1A2 甲基化仍然是独立的预后因素。
本研究表明,CpG 过度甲基化可能是 COL1A2 基因失活的机制,支持 COL1A2 基因可能在 HNSCC 的肿瘤发生中起作用并可能作为重要的生物标志物的假说。