Deng, Kui, Han, Peng, Song, Wei, Wang, Zhuozhong, Zhang, Fan, Xie, Hongyu, Zhao, Weiwei, Xu, Huan, Cai, Yuqing, Rong, Zhiwei, Yu, Xiwen, Cui, Bin-bin, and Li, Kang
Abstract Background Many studies have demonstrated that right-sided colon cancer (RCC) has a higher mortality rate and worse prognosis than left-sided colon cancer (LCC). However, the underlying biological mechanism that can account for these differences is unclear. Methods In this study, plasma metabolic profiles in 147 LCC patients and 105 RCC patients were systematically analyzed by the ultra high performance liquid chromatography quadruple time-of-flight mass spectrometry (UHPLC-QTOF/MS) platform in conjunction with univariate and multivariate statistical analysis. Results Metabolic signatures revealed considerable differences between patients with RCC and LCC, and clear separations were observed between the two groups in partial least-squares discriminant analysis score plots. In total, six metabolites were identified as potential metabolite markers for tumor location in RCC compared with LCC, including upregulated trimethylamine N-oxide and indoxyl sulfate, and downregulated anserine, L-targinine, gamma-glutamyl-gamma-aminobutyraldehyde and pyridoxal 5′-phosphate. These differences highlight that significant alternations occur in the pathways of methane metabolism, arginine and proline metabolism, histidine metabolism, beta-alanine metabolism and vitamin B6 metabolism in RCC compared with LCC. Conclusions Identified biomarkers and metabolic pathways may facilate our understanding of the different mortality rates and prognoses between RCC and LCC. Highlights • Metabolic signatures revealed considerable differences between RCC and LCC. • Six metabolites were identified as potential biomarkers for tumor location. • Metabolomics facilated our understanding of the differences between RCC and LCC. [ABSTRACT FROM AUTHOR]