Huang Sha, Guo Yang, Li Zhexuan, Zhang Yang, Zhou Tong, You Weicheng, Pan Kaifeng, Li Wenqing
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Cancer Epidemiology, Peking University Cancer Hospital & Institute, Beijing 100142, China.
Joint International Research Center of Translational and Clinical Research, Beijing 100142, China.
Cancer Biol Med. 2020 Feb 15;17(1):181-198. doi: 10.20892/j.issn.2095-3941.2019.0348.
Upper gastrointestinal (UGI) cancers, predominantly gastric cancer (GC) and esophageal cancer (EC), are malignant tumor types with high morbidity and mortality rates. Accumulating studies have focused on metabolomic profiling of UGI cancers in recent years. In this systematic review, we have provided a collective summary of previous findings on metabolites and metabolomic profiling associated with GC and EC. A systematic search of three databases (Embase, PubMed, and Web of Science) for molecular epidemiologic studies on the metabolomic profiles of GC and EC was conducted. The Newcastle-Ottawa Scale (NOS) was used to assess the quality of the included articles. A total of 52 original studies were included for review. A number of metabolites were differentially distributed between GC and EC cases and non-cases, including those involved in glycolysis, anaerobic respiration, tricarboxylic acid cycle, and protein and lipid metabolism. Lactic acid, glucose, citrate, and fumaric acid were among the most frequently reported metabolites of cellular respiration while glutamine, glutamate, and valine were among the most commonly reported amino acids. The lipid metabolites identified previously included saturated and unsaturated free fatty acids, aldehydes, and ketones. However, the key findings across studies to date have been inconsistent, potentially due to limited sample sizes and the majority being hospital-based case-control analyses lacking an independent replication group. Studies on metabolomics have thus far provided insights into etiological factors and biomarkers for UGI cancers, supporting the potential of applying metabolomic profiling in cancer prevention and management efforts.
上消化道(UGI)癌,主要是胃癌(GC)和食管癌(EC),是发病率和死亡率都很高的恶性肿瘤类型。近年来,越来越多的研究聚焦于UGI癌的代谢组学分析。在本系统评价中,我们汇总了以往关于与GC和EC相关的代谢物及代谢组学分析的研究结果。我们对三个数据库(Embase、PubMed和Web of Science)进行了系统检索,以查找关于GC和EC代谢组学特征的分子流行病学研究。采用纽卡斯尔-渥太华量表(NOS)评估纳入文章的质量。共纳入52项原始研究进行综述。许多代谢物在GC和EC病例与非病例之间存在差异分布,包括那些参与糖酵解、无氧呼吸、三羧酸循环以及蛋白质和脂质代谢的代谢物。乳酸、葡萄糖、柠檬酸和富马酸是细胞呼吸中最常报道的代谢物,而谷氨酰胺、谷氨酸和缬氨酸是最常报道的氨基酸。先前鉴定出的脂质代谢物包括饱和和不饱和游离脂肪酸、醛类和酮类。然而,迄今为止各研究的关键结果并不一致,这可能是由于样本量有限,且大多数研究是基于医院的病例对照分析,缺乏独立的重复组。因此,代谢组学研究为UGI癌的病因学因素和生物标志物提供了见解,支持了在癌症预防和管理工作中应用代谢组学分析的潜力。