a Department of Gastroenterological Surgery (Surgery II) , Nagoya University Graduate School of Medicine , Nagoya , Japan.
Expert Rev Gastroenterol Hepatol. 2018 Jul;12(7):657-670. doi: 10.1080/17474124.2018.1489233. Epub 2018 Jun 25.
Gastric cancer (GC) is the leading cause of cancer-related death worldwide. Despite recent advances in diagnosis and therapy, the prognosis of patients with GC is poor. Many patients have inoperable disease upon diagnosis or experience recurrent disease after curative gastrectomy. Unfortunately, tumor markers for GC, such as serum carcinoembryonic antigen and carbohydrate antigen 19-9, lack sufficient sensitivity and specificity. Therefore, effective biomarkers are required to detect early GC and to predict tumor recurrence and chemosensitivity. Areas covered: Here we aimed to review recent developments in techniques that improve the detection of aberrant expression of GC-associated molecules, including protein coding genes, microRNAs, long noncoding RNAs, and methylated promoter DNAs. Expert commentary: Detection of genetic and epigenetic alterations in gastric tissue or in the circulation will likely improve the diagnosis and management of GC to achieve significantly improved outcomes.
胃癌(GC)是全球癌症相关死亡的主要原因。尽管近年来在诊断和治疗方面取得了进展,但 GC 患者的预后仍然不佳。许多患者在诊断时已经无法手术,或者在根治性胃切除术后经历复发性疾病。不幸的是,GC 的肿瘤标志物,如血清癌胚抗原和糖类抗原 19-9,缺乏足够的灵敏度和特异性。因此,需要有效的生物标志物来检测早期 GC 并预测肿瘤复发和化疗敏感性。
在这里,我们旨在回顾提高与 GC 相关分子(包括蛋白编码基因、microRNAs、长非编码 RNA 和甲基化启动子 DNA)异常表达检测技术的最新进展。
在胃组织或循环中检测遗传和表观遗传改变可能会改善 GC 的诊断和管理,从而显著提高疗效。