Nadarajan Nithya, Balasubramanian Lakshman Kumar, Kuppannan Suresh, Ramachandran Chandirasekar, Leelakrishnan Venkatakrishnan
J Gastrointest Cancer. 2013 Dec;44(4):444-9. doi: 10.1007/s12029-013-9540-4.
Repression of Runt-related transcription factor 3 (Runx3) gene, a tumor suppressor, has been known to be involved in Helicobacter pylori (H. pylori)-associated gastric carcinogenesis and cancer development. The present study was undertaken to study the Runx3 intronic T/A polymorphism (rs760805) in H. pylori-infected patients and uninfected controls of Tamil Nadu region, South India. Also, Runx3 gene expression, HK alpha (H,K-ATPase) gene expression and the methylation status of the Runx3 CpG island was determined.
In a prospective study, tissue biopsies were collected from 40 H. pylori-infected patients and 40 infection negative controls. Single nucleotide polymorphism analysis was carried out by polymerase chain reaction (PCR)-single-strand conformational polymorphism, and DNA sequencing. Gene expression analysis of Runx3 and HK alpha was carried out using semiquantitative reverse transcriptase-PCR. Methylation analysis of Runx3 CpG island was undertaken using methylationspecific restriction digestion-PCR.
The homozygous TT genotype was found to be the predominant genotype in positive samples and negative controls. No significant variation in gene expression was observed in positive samples and controls with respect to Runx3 and Hk alpha genes. Methylation analysis suggested that there was a lack of methylation except in a few subjects studied.
The present study, first from this region, could neither detect significant repression of the Runx3 and HK alpha genes nor methylation in positive patients studied suggesting a lack of involvement of this tumor suppressor as a risk factor in the H. pylori-associated gastric carcinogenesis in the South Indian population studied.
已知肿瘤抑制因子Runx3相关转录因子3(Runx3)基因的抑制与幽门螺杆菌(H. pylori)相关的胃癌发生及癌症发展有关。本研究旨在对印度南部泰米尔纳德邦地区幽门螺杆菌感染患者及未感染对照者进行Runx3内含子T/A多态性(rs760805)研究。此外,还测定了Runx3基因表达、HKα(H,K - ATP酶)基因表达以及Runx3 CpG岛的甲基化状态。
在一项前瞻性研究中,从40例幽门螺杆菌感染患者和40例感染阴性对照者中采集组织活检样本。通过聚合酶链反应(PCR)-单链构象多态性及DNA测序进行单核苷酸多态性分析。使用半定量逆转录PCR对Runx3和HKα进行基因表达分析。采用甲基化特异性限制性消化PCR对Runx3 CpG岛进行甲基化分析。
在阳性样本和阴性对照中,纯合子TT基因型是主要基因型。在阳性样本和对照中,Runx3和Hkα基因的基因表达未观察到显著差异。甲基化分析表明,除少数研究对象外,不存在甲基化现象。
本研究首次来自该地区,在研究的阳性患者中既未检测到Runx3和HKα基因的显著抑制,也未检测到甲基化,这表明在该印度南部人群中,这种肿瘤抑制因子作为幽门螺杆菌相关胃癌发生的危险因素未发挥作用。