Yang Ruirui, Fu Yun, Zeng Ying, Xiang Mengqin, Yin Yufang, Li Li, Xu Haifan, Zhong Jing, Zeng Xi
Hunan Province Key Laboratory of Tumor Cellular and Molecular Pathology, Cancer Research Institute, University of South China, Hengyang, Hunan 421001, P.R. China.
Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China, Hengyang, Hunan 421001, P.R. China.
Biomed Rep. 2017 Apr;6(4):429-434. doi: 10.3892/br.2017.862. Epub 2017 Feb 20.
Gastric cancer (GC) is a common type of cancer, particularly in China. Numerous studies have demonstrated that circulating microRNAs (miRNAs) have potential applications as noninvasive biomarkers for cancer diagnosis and prognosis. Microarray-based serum miRNA profiling was performed on the serum of 12 paired pre- and post-operative GC patients to screen differentially expressed serum miRNAs. Twelve different serum miRNAs between pre- and post-operative GC patients were identified. Those miRNAs were verified by real-time quantitative polymerase chain reaction in 110 paired pre- and post-operative serum samples from 55 GC patients. miR-20a was confirmed and demonstrated potential as a GC-associated biomarker. Furthermore, the levels of serum miR-20a were significantly different between GC, nasopharyngeal cancer, colorectal carcinoma, breast cancer and non-cancerous controls. In addition, it was found that serum miR-20a levels correlated with age, tumor stage, differentiated degree and lymph node metastasis in GC. Survival analysis indicated that GC patients with elevated levels of serum miR-20a had poor survival. Thus, serum miR-20a may serve as a molecular marker for diagnosis, evaluating therapeutic efficacy and prognosis, as well as monitoring recurrence in GC patients.
胃癌(GC)是一种常见的癌症类型,在中国尤为如此。众多研究表明,循环微RNA(miRNA)作为癌症诊断和预后的非侵入性生物标志物具有潜在应用价值。对12例配对的GC患者术前和术后血清进行基于微阵列的血清miRNA分析,以筛选差异表达的血清miRNA。在GC患者术前和术后血清中鉴定出12种不同的血清miRNA。这些miRNA在来自55例GC患者的110对术前和术后血清样本中通过实时定量聚合酶链反应进行了验证。miR-20a得到确认,并显示出作为GC相关生物标志物的潜力。此外,GC、鼻咽癌、结直肠癌、乳腺癌患者与非癌症对照者之间血清miR-20a水平存在显著差异。另外,发现血清miR-20a水平与GC患者的年龄、肿瘤分期、分化程度及淋巴结转移相关。生存分析表明,血清miR-20a水平升高的GC患者生存情况较差。因此,血清miR-20a可作为GC患者诊断、评估治疗疗效和预后以及监测复发的分子标志物。