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Metabolome-wide association identifies altered metabolites and metabolic pathways in the serum of patients with cholangiocarcinoma.
Jackson, Linsey E; Tomlinson, Jennifer L; Alva-Ruiz, Roberto; Gregory, Lindsey A; Byeon, Seul Kee; Abdelrahman, Amro M; Mun, Dong-Gi; Grant, Caroline W; Fogarty, Zachary C; Wang, Chen; Roberts, Lewis R; Graham, Rondell P; Borad, Mitesh J; Ilyas, Sumera I; Gores, Gregory J; Pandey, Akhilesh; Athreya, Arjun P; Smoot, Rory L.
Afiliación
  • Jackson LE; Center For Clinical and Translational Science, Mayo Clinic, Rochester, MN, USA.
  • Tomlinson JL; Department of Surgery, Mayo Clinic, Rochester, MN, USA.
  • Alva-Ruiz R; Department of Surgery, Mayo Clinic, Rochester, MN, USA.
  • Gregory LA; Department of Surgery, Mayo Clinic, Rochester, MN, USA.
  • Byeon SK; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Abdelrahman AM; Department of Surgery, Mayo Clinic, Rochester, MN, USA.
  • Mun DG; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Grant CW; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN, USA.
  • Fogarty ZC; Department of Computational Biology, Mayo Clinic, Rochester, MN, USA.
  • Wang C; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
  • Roberts LR; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
  • Graham RP; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Borad MJ; Division of Hematology and Medical Oncology, Mayo Clinic, Phoenix, AZ, USA.
  • Ilyas SI; Department of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
  • Gores GJ; Mayo Clinic Comprehensive Cancer Center, Mayo Clinic, Phoenix, AZ, USA.
  • Pandey A; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
  • Athreya AP; Department of Immunology, Mayo Clinic, Rochester, MN, USA.
  • Smoot RL; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
JHEP Rep ; 6(6): 101068, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38882601
ABSTRACT
Background &

Aims:

Metabolomic and lipidomic analyses provide an opportunity for novel biological insights. Cholangiocarcinoma (CCA) remains a highly lethal cancer with limited response to systemic, targeted, and immunotherapeutic approaches. Using a global metabolomics and lipidomics platform, this study aimed to discover and characterize metabolomic variations and associated pathway derangements in patients with CCA.

Methods:

Leveraging a biospecimen collection, including samples from patients with digestive diseases and normal controls, global serum metabolomic and lipidomic profiling was performed on 213 patients with CCA and 98 healthy controls. The CCA cohort of patients included representation of intrahepatic, perihilar, and distal CCA tumours. Metabolome-wide association studies utilizing multivariable linear regression were used to perform case-control comparisons, followed by pathway enrichment analysis, CCA subtype analysis, and disease stage analysis. The impact of biliary obstruction was evaluated by repeating analyses in subsets of patients only with normal bilirubin levels.

Results:

Of the 420 metabolites that discriminated patients with CCA from controls, decreased abundance of cysteine-glutathione disulfide was most closely associated with CCA. Additional conjugated bile acid species were found in increased abundance even in the absence of clinically relevant biliary obstruction denoted by elevated serum bilirubin levels. Pathway enrichment analysis also revealed alterations in caffeine metabolism and mitochondrial redox-associated pathways in the serum of patients with CCA.

Conclusions:

The presented metabolomic and lipidomic profiling demonstrated multiple alterations in the serum of patients with CCA. These exploratory data highlight novel metabolic pathways in CCA and support future work in therapeutic targeting of these pathways and the development of a precision biomarker panel for diagnosis. Impact and implications Cholangiocarcinoma (CCA) is a highly lethal hepatobiliary cancer with limited treatment response, highlighting the need for a better understanding of the disease biology. Using a global metabolomics and lipidomics platform, we characterized distinct changes in the serum of 213 patients with CCA compared with healthy controls. The results of this study elucidate novel metabolic pathways in CCA. These findings benefit stakeholders in both the clinical and research realms by providing a foundation for improved disease diagnostics and identifying novel targets for therapeutic design.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: JHEP Rep Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: JHEP Rep Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos