# Non-invasive tape sampling of tryptophan and kynurenine in relation to phenylalanine and tyrosine from melanoma and adjacent non-lesional skin: A pilot study

**Authors:** Skaidre Jankovskaja, Peter Spégel, Kari Nielsen, Sebastian Björklund, Jeremy Bost, Johan Engblom, Gustav Christensen, Oksana Rogova, Maxim Morin, Merete Haedersdal, Martin Malmsten, Chris D. Anderson, Tautgirdas Ruzgas, Krishnendu Sinha, Krishnendu Sinha, Krishnendu Sinha, Krishnendu Sinha

PMC · DOI: 10.1371/journal.pone.0326457 · PLOS One · 2025-06-24

## TL;DR

This pilot study shows that non-invasive tape sampling can detect higher levels of certain metabolites on melanoma skin compared to healthy skin, possibly due to a weakened skin barrier.

## Contribution

The study introduces non-invasive tape sampling as a method to detect metabolic changes in melanoma skin.

## Key findings

- Melanoma lesions showed significantly higher levels of Tyr, Phe, Trp, and Kyn compared to non-lesional skin.
- Skin resistance in melanoma lesions was half that of non-lesional skin, indicating a compromised skin barrier.
- Trp depletion was suggested as metabolite levels indicated higher Trp conversion to Kyn in melanoma.

## Abstract

To evade immunosurveillance many cancers convert tryptophan (Trp) into kynurenine (Kyn), which induces immunotolerance and suppresses immune responses. Elevated Kyn amounts have been found in blood from patients with cutaneous melanoma. This study aimed to investigate whether higher Kyn abundance and lower Trp abundance can be detected on the surface of cutaneous melanoma lesions compared with adjacent non-lesional skin.

Sixteen patients with suspected melanomas were enrolled in this study. All lesions were excised and histopathologically diagnosed: 7 lesions were diagnosed as invasive malignant melanomas (MM), 6 as melanomas in situ (MIS), and 3 as benign lesions (BL). Non-invasive metabolite sampling was performed by tape stripping of suspected skin lesions and adjacent healthy non-lesional (NL) skin. Trp, Kyn, tyrosine (Tyr), and phenylalanine (Phe) were quantified by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Electrical impedance spectroscopy (EIS) measurements were conducted to assess skin barrier integrity.

Levels of all metabolites, Tyr (x6), Phe (x6), Trp (x5), and Kyn (x3), were significantly higher in MM lesions compared with adjacent NL skin, resulting in an elevated Trp/Kyn ratio. Trp levels increased less than Phe and Tyr levels, suggesting a potential increase in Trp depletion. Skin resistance in MM lesions was half that of NL skin. No differences were observed between MIS or BL and NL skin.

Non-invasive skin sampling revealed elevated Tyr, Phe, Trp and Kyn levels in MM skin, which is likely the result of compromised skin barrier at this stage of cutaneous melanoma.

## Linked entities

- **Chemicals:** tryptophan (PubChem CID 1148), kynurenine (PubChem CID 846), tyrosine (PubChem CID 1153), phenylalanine (PubChem CID 994)
- **Diseases:** melanoma (MONDO:0005105), cutaneous melanoma (MONDO:0005012)

## Full-text entities

- **Diseases:** cutaneous melanoma (MESH:C562393), BL (MESH:D001932), skin lesions (MESH:D012871), MIS (MESH:D008545), cancers (MESH:D009369)
- **Chemicals:** Trp (MESH:D014364), Phe (MESH:D010649), Kyn (MESH:D007737), Tyr (MESH:D014443)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12186910/full.md

## References

85 references — full list in the complete paper: https://tomesphere.com/paper/PMC12186910/full.md

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Source: https://tomesphere.com/paper/PMC12186910