Charting the metabolic biogeography of the colorectum in cancer : challenging the right sided versus left sided classification

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Jain, Abhishek and Morris, Montana T. and Berardi, Domenica and Arora, Trisha and Domingo-Almenara, Xavier and Paty, Philip B. and Rattray, Nicholas J. W. and Kerekes, Daniel and Lu, Lingeng and Khan, Sajid A. and Johnson, Caroline H. (2024) Charting the metabolic biogeography of the colorectum in cancer : challenging the right sided versus left sided classification. Molecular Cancer, 23 (1). 211. ISSN 1476-4598 (https://doi.org/10.1186/s12943-024-02133-5)

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Abstract

Objective: Colorectal cancer (CRC) is conventionally classified as right sided, left sided, and rectal cancer. Clinicopathological, molecular features and risk factors do not change abruptly along the colorectum, and variations exist even within the refined subsites, which may contribute to inconsistencies in the identification of clinically relevant CRC biomarkers. We generated a CRC metabolome map to describe the association between metabolites, diagnostic and survival heterogeneity in cancers of different subsites of the colorectum. Design: Utilizing 372 patient-matched tumor and normal mucosa tissues, liquid chromatography-mass spectrometry was applied to examine metabolomic profiles along seven subsites of the colorectum: cecum (n = 63), ascending colon (n = 44), transverse colon (n = 32), descending colon (n = 28), sigmoid colon (n = 75), rectosigmoid colon (n = 38), and rectum (n = 92). Results: 39 and 70 significantly altered metabolites (including bile acids, lysophosphatidylcholines and lysophosphatidylethanolamines) among tumors and normal mucosa, respectively, showed inter-subsite metabolic heterogeneity between CRC subsites. Gradual changes in metabolite abundances with significantly linear trends from cecum to rectum were observed: 23 tumor-specific metabolites, 30 normal mucosa-specific metabolites, and 15 metabolites in both tumor and normal mucosa, had concentration gradients across the colorectum, and is disease status dependent. The metabolites that showed a linear trend included bile acids, amino acids, lysophosphatidylcholines, and lysophosphatidylethanolamines. Comparison of tumors to patient-matched normal mucosa revealed metabolite changes exclusive to each subsite, thereby further highlighting differences in cancer metabolism across the 7 subsites of the colorectum. Furthermore, metabolites associated with survival were different and unique to each subsite. Finally, an interactive and publicly accessible CRC metabolome database was designed to enable access and utilization of this rich data resource (https://colorectal-cancer-metabolome.com/yale-university). Conclusions: Gradual changes exist in metabolite abundances from the cecum to the rectum. The association between patient survival and distinct metabolites with anatomic subsite of the colorectum, reveals differences between cancers across the colorectum. These inter-subsite metabolic heterogeneities enrich the current understanding and substantiate previous studies that have challenged the conventional classification of right-sided, left-sided, and rectal cancers, by identifying specific metabolites that offer new biological insights into CRC subsite heterogeneity. The database designed in this study will enable researchers to delve into granular information on the CRC metabolome, which until now has not been available.

ORCID iDs

Jain, Abhishek, Morris, Montana T., Berardi, Domenica, Arora, Trisha, Domingo-Almenara, Xavier, Paty, Philip B., Rattray, Nicholas J. W. ORCID logoORCID: https://orcid.org/0000-0002-3528-6905, Kerekes, Daniel, Lu, Lingeng, Khan, Sajid A. and Johnson, Caroline H.;
CORE (COnnecting REpositories)