Lee Hyunsu, Lee Jae-Ho, Kim Dong-Choon, Hwang IlSeon, Kang Yu-Na, Gwon Gi-Jeong, Choi In-Jang, Kim Shin
Department of Anatomy, School of Medicine, Keimyung University, Daegu, Republic of Korea E-mail :
Asian Pac J Cancer Prev. 2015;16(1):87-90. doi: 10.7314/apjcp.2015.16.1.87.
Alterations in mitochondrial DNA (mtDNA) have been studied in various cancers. However, the clinical value of mtDNA copy number (mtCN) alterations in gastric cancer (GC) is poorly understood. In the present study, we investigated whether alterations in mtCNs might be associated with clinicopathological parameters in GC cases. mtCN was measured in 109 patients with GC by quantitative real-time PCR. Then, correlations with clinicopathological characteristics were analyzed. mtCN was elevated in 64.2% of GC tissues compared with paired, adjacent, non-cancerous tissue. However, the observed alterations in mtCN were not associated with any clinicopathological characteristics, including age, gender, TN stage, Lauren classification, lymph node metastasis, and depth of invasion. Moreover, Kaplan-Meier survival curves revealed that mtCN was not significantly associated with the survival of GC patients. In this study, we demonstrated that mtCN was not a significant marker for predicting clinical characteristics or prognosis in GC.
线粒体DNA(mtDNA)的改变已在多种癌症中得到研究。然而,胃癌(GC)中线粒体DNA拷贝数(mtCN)改变的临床价值却知之甚少。在本研究中,我们调查了mtCN的改变是否可能与GC病例的临床病理参数相关。通过定量实时PCR检测了109例GC患者的mtCN。然后,分析了其与临床病理特征的相关性。与配对的相邻非癌组织相比,64.2%的GC组织中mtCN升高。然而,观察到的mtCN改变与任何临床病理特征均无关联,包括年龄、性别、TN分期、Lauren分类、淋巴结转移和浸润深度。此外,Kaplan-Meier生存曲线显示,mtCN与GC患者的生存无显著相关性。在本研究中,我们证明mtCN不是预测GC临床特征或预后的重要标志物。