Department of Health Technology and Informatics, Faculty of Health and Social Sciences, Hong Kong Polytechnic University , Hong Kong , Hong Kong Special Administrative Region, China.
Department of Clinical Oncology, Queen Elizabeth Hospital , Kowloon , Hong Kong Special Administrative Region, China.
Expert Rev Mol Diagn. 2019 Oct;19(10):863-874. doi: 10.1080/14737159.2019.1660645. Epub 2019 Aug 29.
: Gastric cancer (GC) is the fifth most common cancer and confers the second-highest mortality among other cancers. Improving the survival rates of GC patients requires prompt and accurate diagnosis and effective treatment which is often preceded by the poorly understood pathogenic mechanisms. : This literature review aims to summarize current understanding of genetic and molecular alterations that promote carcinogenesis including (1) activation of oncogenes, (2) overexpression of growth factors, receptors and matrix metalloproteinases, (3) inactivation of tumor suppressor genes, DNA repair genes, and cell adhesion molecules and (4) alterations of cell-cycle regulators that regulate biological characteristics of cancer cells. Moreover, the significance of molecular biomarkers such as micro-RNAs (miRNAs) and long non-coding RNAs (lncRNAs) and advanced molecular techniques including droplet digital polymerase chain reaction (ddPCR), quantitative PCR (qPCR) and next-generation sequencing (NGS) are also discussed. : A GC-specific panel of biomarkers based on the NGS or ddPCR has the potential for diagnosis, prognosis, and monitoring treatment response in GC patients. Despite the requirements for validation in larger population in clinical studies, race-specific differences in the gene panel have also to be examined by performing the clinical trials in subjects with different races.
胃癌(GC)是第五种最常见的癌症,也是其他癌症中死亡率第二高的癌症。提高 GC 患者的生存率需要及时准确的诊断和有效的治疗,而这通常需要了解了解甚少的发病机制。
本文献综述旨在总结促进癌变的遗传和分子变化的现有认识,包括(1)癌基因的激活,(2)生长因子、受体和基质金属蛋白酶的过度表达,(3)肿瘤抑制基因、DNA 修复基因和细胞粘附分子的失活,以及(4)调节癌细胞生物学特性的细胞周期调节剂的改变。此外,还讨论了分子生物标志物(如 micro-RNAs(miRNAs)和长非编码 RNA(lncRNAs))和先进的分子技术(如液滴数字聚合酶链反应(ddPCR)、定量聚合酶链反应(qPCR)和下一代测序(NGS))的重要性。
基于 NGS 或 ddPCR 的 GC 特异性生物标志物组合具有在 GC 患者中进行诊断、预后和监测治疗反应的潜力。尽管需要在更大的人群中进行临床研究验证,但也需要通过在不同种族的受试者中进行临床试验来检查基因组合中的种族特异性差异。