Evidence map›Paper›PMID 41526979›Full record

ArticleBiology direct2026

Solute carrier family (SLC) amino acid transporters are upregulated in cutaneous squamous cell carcinoma.

Alessia Petrilli, Damiano Barnaba, Mara Mancini, Luca Fania, Francesco Ricci, Elena Dellambra, Gerry Melino, Eleonora Candi, Artem Smirnov

Abstract read
In one paragraph

Article in Biology direct, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Alessia PetrilliDept. of Experimental Medicine, University of Rome Tor Vergata, TOR, Rome, 00133, Italy.
Damiano BarnabaDept. of Experimental Medicine, University of Rome Tor Vergata, TOR, Rome, 00133, Italy.
Mara ManciniDept. of Experimental Medicine, University of Rome Tor Vergata, TOR, Rome, 00133, Italy.
Luca FaniaBiochemistry Laboratory, Istituto Dermopatico Immacolata (IDI-IRCCS), Rome, 00144, Italy.
Francesco RicciBiochemistry Laboratory, Istituto Dermopatico Immacolata (IDI-IRCCS), Rome, 00144, Italy.
Elena DellambraBiochemistry Laboratory, Istituto Dermopatico Immacolata (IDI-IRCCS), Rome, 00144, Italy.
Gerry MelinoDept. of Experimental Medicine, University of Rome Tor Vergata, TOR, Rome, 00133, Italy.
Eleonora CandiDept. of Experimental Medicine, University of Rome Tor Vergata, TOR, Rome, 00133, Italy.
Artem SmirnovDept. of Experimental Medicine, University of Rome Tor Vergata, TOR, Rome, 00133, Italy. artem.smirnov@uniroma2.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Solute carrier family (SLC) amino acid transporters play key role in maintaining a continuous supply of nutrients to cancer cells. Non melanoma skin tumours, the most common cancer type worldwide, undergo extensive metabolic rewiring to survive under hostile conditions. To adapt to nutrient-poor microenvironment, tumour cells often boost expression of the key metabolic enzymes. However, the role of the amino acid transporters and their therapeutic potential in non-melanoma skin cancer remain unclear. Here, we analyse publicly available transcriptomics data and identify several amino acid transporters that are strongly upregulated in skin cancer, including neutral amino acid transporter LAT1. LAT1 is overexpressed in proliferating basal-like cells within skin tumours and its level decreases during epidermal differentiation. Furthermore, we show that cutaneous squamous cell carcinoma cells rely on citrulline to survive under arginine scarcity and LAT1 is essential for citrulline import. Pharmacological inhibition of LAT1 by the small compound JPH203 sensitises cells to arginine deprivation. Altogether, we show that amino transporter LAT1 plays an important role in cutaneous squamous cell carcinoma growth in low arginine conditions and highlight its potential as a therapeutic target.

Indexed as

Amino Acid Transport SystemsCarcinoma, Squamous CellCutaneous Squamous Cell CarcinomaGene Expression Regulation, NeoplasticLarge Neutral Amino Acid-Transporter 1Skin NeoplasmsUp-RegulationArginineCell Line, TumorCitrullineHumansAmino Acid Transport SystemsArginineCitrullineLarge Neutral Amino Acid-Transporter 1Amino acid metabolismArginineLAT1Skin cancer

Identifiers

PMID41526979
PMCPMC12888701

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.