# ¹H-NMR serum metabolomic profiling from clinical routine identifies signatures of progressive melanoma metastasis

**Authors:** Frank Friedrich Gellrich, Cosima Hufnagel, Alexander M. Funk, Sophie Jonas, Heidi Altmann, Sarah Hobelsberger, Julian Steininger, Christina Feige, Alpaslan Tasdogan, Triantafyllos Chavakis, Stefan Beissert, Friedegund Meier, Peter Mirtschink, Gerald Steiner

PMC · DOI: 10.1038/s41598-026-37118-5 · Scientific Reports · 2026-01-30

## TL;DR

This study uses blood metabolite profiles to detect active melanoma metastasis, finding specific metabolic changes linked to disease progression.

## Contribution

The study identifies ¹H-NMR-based serum metabolic signatures for active melanoma metastasis in a large clinical cohort.

## Key findings

- Seven significant metabolites (pyruvate, phenylalanine, acetoacetate, glutamate, glucose, citrate, histidine) are associated with active metastasis.
- Metabolic signatures vary with ICI therapy and BRAF status, showing potential for personalized biomarker panels.
- ¹H-NMR serum metabolomics detects systemic metabolic alterations with moderate accuracy in real-world settings.

## Abstract

Early detection of active melanoma metastasis is crucial. Serum metabolomics may offer non-invasive biomarkers, but real-world applicability needs validation. This study aimed to identify ¹H-NMR-based serum metabolic signatures for active metastasis in a large clinical cohort. Serum from 963 melanoma patients (1698 samples) underwent ¹H-NMR spectroscopy. Patients were classified by active metastasis status. OPLS-DA and RFE followed by logistic regression models were developed on a patient-level training/test split. Subgroup analyses assessed signatures related to Immune Checkpoint Inhibitor (ICI) therapy, brain metastases, and BRAF status. Models for active metastasis showed moderate test set discrimination (Area Under the Curve [AUCs]: OPLS-DA 0.609, RFE 0.630). The RFE-model highlighted seven significant metabolites: increased pyruvate, phenylalanine, acetoacetate, glutamate, glucose, and decreased histidine and citrate were associated with active metastasis. OPLS-DA yielded concordant metabolites. Subgroup analyses revealed distinct metabolic associations, e.g., for ICI therapy (citrate, RFE AUC 0.721) and BRAF status (acetate, RFE AUC 0.655), but limited performance for brain metastases (RFE AUC 0.553). ¹H-NMR serum metabolomics detects systemic metabolic alterations of active melanoma metastasis with moderate accuracy in a real-world setting. Identified disruptions in energy and amino acid metabolism offer pathobiological insights and warrant investigation for multimodal biomarker panels.

The online version contains supplementary material available at 10.1038/s41598-026-37118-5.

## Linked entities

- **Chemicals:** pyruvate (PubChem CID 107735), phenylalanine (PubChem CID 994), acetoacetate (PubChem CID 6971017), glutamate (PubChem CID 611), glucose (PubChem CID 5793), citrate (PubChem CID 31348), histidine (PubChem CID 773), acetate (PubChem CID 175)
- **Diseases:** melanoma (MONDO:0005105)

## Full-text entities

- **Genes:** ACSS2 (acyl-CoA synthetase short chain family member 2) [NCBI Gene 55902] {aka ACAS2, ACECS, ACS, ACSA, AceCS1, dJ1161H23.1}, SLC7A5 (solute carrier family 7 member 5) [NCBI Gene 8140] {aka 4F2LC, CD98, D16S469E, E16, LAT1, MPE16}, ACLY (ATP citrate lyase) [NCBI Gene 47] {aka ACL, ATPCL, CLATP}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, VIP (vasoactive intestinal peptide) [NCBI Gene 7432] {aka PHM27}, PDP1 (pyruvate dehydrogenase phosphatase catalytic subunit 1) [NCBI Gene 54704] {aka PDH, PDP, PDPC, PDPC 1, PPM2A, PPM2C}, PAH (phenylalanine hydroxylase) [NCBI Gene 5053] {aka PH, PKU, PKU1}
- **Diseases:** Metastasis (MESH:D009362), node (MESH:D012804), melanocytic (MESH:D009508), inflammation (MESH:D007249), uveal or ciliary body melanoma (MESH:C536494), Skin Cancer (MESH:D012878), Stage III (MESH:D062706), cutaneous and mucosal melanoma (MESH:C562393), CPMG (MESH:C000654764), Cancer (MESH:D009369), Melanoma (MESH:D008545)
- **Chemicals:** isoleucine (MESH:D007532), carbon (MESH:D002244), acetate (MESH:D000085), acetoacetate (MESH:C016635), acetone (MESH:D000096), alanine (MESH:D000409), proline (MESH:D011392), ketone body (MESH:D007657), nucleotide (MESH:D009711), histidine (MESH:D006639), Tricarboxylic Acid (MESH:D014233), acetyl-CoA (MESH:D000105), pyruvate (MESH:D019289), glucose (MESH:D005947), amino acid (MESH:D000596), glutamate (MESH:D018698), fatty acid (MESH:D005227), lipid (MESH:D008055), TCA (MESH:D014238), phenylalanine (MESH:D010649), 3-hydroxybutyrate (MESH:D020155), nitrogen (MESH:D009584), lactate (MESH:D019344), citrate (MESH:D019343), glycine (MESH:D005998), alpha-ketoglutarate (MESH:D007656), ketone (MESH:D007659), 1H (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12881348