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April 5, 2026Cancer Research0 citations

Abstract 6132: Linking metabolic reprogramming to JAK-STAT signaling in triple-negative breast cancer brain metastasis

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JMJayshree MishraNKNarendra Kumar

Key Points

  • The aim is to uncover how metabolic reprogramming in TNBC cells contributes to their survival and adaptation in the brain microenvironment.
  • Conducted integrated metabolomic and transcriptomic analyses in a TNBC brain metastasis xenograft mouse model.
  • Performed metabolite profiling using liquid chromatography-mass spectrometry.
  • Identified unique metabolites in brain metastases and serum through pathway enrichment analysis.
  • Cross-referenced metabolite findings with gene expression data for network analysis.
  • Identified RNF125 as a central regulatory node linking metabolic pathways to JAK-STAT signaling.
  • Found that RNF125 upregulation correlates inversely with JAK3 activity.
  • Suggested RNF125 plays a role in cytokine signaling modulation for TNBC adaptation in the brain.

Abstract

Abstract Introduction: Triple-negative breast cancer (TNBC) is an aggressive breast cancer subtype disproportionately affects younger patients and associated with high recurrence rates and rapid disease progression. TNBC cells that colonize the brain undergo extensive metabolic reprogramming to survive in this specialized microenvironment. Understanding the mechanisms by which TNBC cells adapt their metabolism and signaling networks to thrive in the brain niche is critical to uncovering novel vulnerabilities for therapeutic intervention. Materials and Methods: To address this knowledge gap, we conducted integrated metabolomic and transcriptomic analyses utilizing a TNBC brain metastasis (BM) xenograft mouse model, with validation in human patient-derived tissues. Metabolite profiling was performed using liquid chromatography-mass spectrometry equipped with an ACQUITY UPLC BEH C18 column. Matched samples from primary tumors, brain metastases, and serum were analyzed. Metabolite deconvolution employed AMDIS software, and compound identification was cross-referenced with NIST and HMDB spectral databases. Unique metabolites enriched in brain metastases and serum were identified and subjected to pathway enrichment analysis using MetaboAnalyst. To integrate metabolic findings with gene expression, pathway-associated genes were cross-referenced against transcriptomic datasets (GEO GSE76714), enabling network analysis of metabolite-gene interactions. Results: Our integrative analyses revealed that RNF125, an E3 ubiquitin ligase involved in immune regulation and oncogenesis, functions as a central regulatory node connecting metabolic pathways to the JAK-STAT signaling axis. RNF125 upregulation was inversely correlated with JAK3 activity, suggesting a role in modulating cytokine signaling to promote TNBC cell adaptation within the brain microenvironment. Conclusion: This study identifies RNF125 as a novel biomarker and potential therapeutic target in TNBC brain metastasis. Citation Format: Jayshree Mishra, Narendra Kumar. Linking metabolic reprogramming to JAK-STAT signaling in triple-negative breast cancer brain metastasis abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6132.

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Cite This Study

Mishra et al. (2026) studied this question.

synapsesocial.com/papers/69d1fde4a79560c99a0a43a2https://doi.org/10.1158/1538-7445.am2026-6132
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