Frontiers in Oncology (Jun 2024)

Integrating metabolic profiling of pancreatic juice with transcriptomic analysis of pancreatic cancer tissue identifies distinct clinical subgroups

  • Alessandra Pulvirenti,
  • Alessandra Pulvirenti,
  • Marialuisa Barbagallo,
  • Anna Rita Putignano,
  • Antonio Pea,
  • Antonio Pea,
  • Rebecca Polidori,
  • Rebecca Polidori,
  • Rosie Upstill-Goddard,
  • Nina Cortese,
  • Paolo Kunderfranco,
  • Laura Brunelli,
  • Giulia De Simone,
  • Roberta Pastorelli,
  • Paola Spaggiari,
  • Gennaro Nappo,
  • Gennaro Nappo,
  • Nigel B. Jamieson,
  • Nigel B. Jamieson,
  • Alessandro Zerbi,
  • Alessandro Zerbi,
  • David K. Chang,
  • David K. Chang,
  • Giovanni Capretti,
  • Giovanni Capretti,
  • Federica Marchesi,
  • Federica Marchesi

DOI
https://doi.org/10.3389/fonc.2024.1405612
Journal volume & issue
Vol. 14

Abstract

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IntroductionMetabolic reprogramming is a hallmark feature of pancreatic ductal adenocarcinoma (PDAC). A pancreatic juice (PJ) metabolic signature has been reported to be prognostic of oncological outcome for PDAC. Integration of PJ profiling with transcriptomic and spatial characterization of the tumor microenvironment would help in identifying PDACs with peculiar vulnerabilities.MethodsWe performed a transcriptomic analysis of 26 PDAC samples grouped into 3 metabolic clusters (M_CL) according to their PJ metabolic profile. We analyzed molecular subtypes and transcriptional differences. Validation was performed by multidimensional imaging on tumor slides.ResultsPancreatic juice metabolic profiling was associated with PDAC transcriptomic molecular subtypes (p=0.004). Tumors identified as M_CL1 exhibited a non-squamous molecular phenotype and demonstrated longer survival. Enrichment analysis revealed the upregulation of immune genes and pathways in M_CL1 samples compared to M_CL2, the group with worse prognosis, a difference confirmed by immunofluorescence on tissue slides. Enrichment analysis of 39 immune signatures by xCell confirmed decreased immune signatures in M_CL2 compared to M_CL1 and allowed a stratification of patients associated with longer survival.DiscussionPJ metabolic fingerprints reflect PDAC molecular subtypes and the immune microenvironment, confirming PJ as a promising source of biomarkers for personalized therapy.

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