Pamungkas Aryo D, Park Changyoung, Lee Sungyong, Jee Sun Ha, Park Youngja H
Metabolomics Laboratory, College of Pharmacy, Korea University, Sejong, 30019, Korea.
Korea University Guro Hospital 148, Gurodong-ro, Guro-gu, Seoul, 08308, Korea.
Respir Res. 2016 Aug 9;17(1):100. doi: 10.1186/s12931-016-0419-3.
The cancer death rate escalated during 20th century. In South Korea, lung cancer is expected to contribute 12,736 deaths in men, the highest amount among all cancers. Several risk factors may increase the chance to acquiring lung cancer, with mostly related to exogenous compounds found in cigarette smoke and synthetic manufacturing materials. As the mortality rate of lung cancer increases, deeper understanding is necessary to explore risk factors that may lead to this malignancy. In this regard, this study aims to apply high resolution metabolomics (HRM) using LC-MS to detect significant compounds that might contribute in inducing lung cancer and find the correlation of these compounds to the subjects' smoking habit.
The comparison was made between healthy control and lung cancer groups for metabolic differences. Further analyses to determine if these differences are related to tobacco-induced lung cancer (past-smoker control vs. past-smoker lung cancer patients (LCPs) and non-smoker control vs. current-smoker LCPs) were selected. The univariate analysis was performed, including a false discovery rate (FDR) of q = 0.05, to determine the significant metabolites between the analyses. Hierarchical clustering analysis (HCA) was done to discriminate metabolites between the control and case subjects. Selected compounds based on significant m/z features of human serum then experienced MS/MS examination, showing that for many m/z, the patterns of ion dissociation matched with standards. Then, the significant metabolites were identified using Metlin database and features were mapped on the human metabolic pathway mapping tool of the Kyoto Encyclopedia of Genes and Genomes (KEGG).
Using metabolomics-wide association studies, metabolic changes were observed among control group and lung cancer patients. Bisphenol A (211.11, M + H-H2O), retinol (287.23, M + H) and L-proline (116.07, M + H) were among the significant compounds found to have contributed in the discrimination between these groups, suggesting that these compounds might be related in the development of lung cancer. Retinol has been seen to have a correlation with smoking while both bisphenol A and L-proline were found to be unrelated.
Two potential biomarkers, retinol and L-proline, were identified and these findings may create opportunities for the development of new lung cancer diagnostic tools.
20世纪癌症死亡率不断攀升。在韩国,预计男性肺癌死亡人数将达12736人,在所有癌症中占比最高。多种风险因素可能会增加患肺癌的几率,其中大部分与香烟烟雾及合成制造材料中的外源性化合物有关。随着肺癌死亡率的上升,有必要深入了解可能导致这种恶性肿瘤的风险因素。在这方面,本研究旨在应用液相色谱-质谱联用的高分辨率代谢组学(HRM)技术,检测可能诱发肺癌的重要化合物,并找出这些化合物与受试者吸烟习惯之间的关联。
对健康对照组和肺癌组的代谢差异进行比较。进一步分析以确定这些差异是否与烟草诱发的肺癌相关(既往吸烟者对照组与既往吸烟者肺癌患者(LCPs),以及非吸烟者对照组与现吸烟者LCPs)。进行单变量分析,包括错误发现率(FDR)为q = 0.05,以确定分析之间的显著代谢物。进行层次聚类分析(HCA)以区分对照组和病例组之间 的代谢物。基于人血清的显著m/z特征选择的化合物随后进行了串联质谱(MS/MS)检测,结果表明,对于许多m/z,离子解离模式与标准匹配。然后,使用Metlin数据库鉴定显著代谢物,并将特征映射到京都基因与基因组百科全书(KEGG)的人类代谢途径映射工具上。
通过代谢组学全基因组关联研究,在对照组和肺癌患者中观察到了代谢变化。双酚A(211.11,M + H - H2O)、视黄醇(287.23,M + H)和L-脯氨酸(116.07,M + H)是在区分这些组时发现的重要化合物,表明这些化合物可能与肺癌的发生有关。视黄醇与吸烟有关,而双酚A和L-脯氨酸均与吸烟无关。
确定了两种潜在的生物标志物,视黄醇和L-脯氨酸,这些发现可能为开发新的肺癌诊断工具创造机会。