Evidence map›Paper›PMID 41815791›Full record

ReviewJID innovations : skin science from molecules to population health2026

The tumor microenvironment of cutaneous squamous cell carcinoma in high-risk patient groups: A scoping review.

Wandong Wang, Clara Harrs, Maria C Bolling, Barbara Horváth, Gilles F H Diercks, Emőke Rácz

Abstract readReview
In one paragraph

Review in JID innovations : skin science from molecules to population health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Wandong WangDepartment of Dermatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Clara HarrsCenter for Blistering Diseases, Department of Pathology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Maria C BollingDepartment of Dermatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Barbara HorváthDepartment of Dermatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Gilles F H DiercksDepartment of Dermatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Emőke RáczDepartment of Dermatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous squamous cell carcinoma (cSCC) is a prevalent skin cancer in the general population that poses so far unresolved challenges in high-risk groups such as organ transplant recipients and individuals with recessive dystrophic epidermolysis bullosa. Although most cases of cSCC respond well to standard treatments, these 2 groups often face more aggressive disease, characterized by higher rates of metastasis and cancer-specific mortality. The tumor microenvironment plays a pivotal role in cSCC progression, influencing tumor growth, immune evasion, and therapy response. Therefore, this scoping review aims to systematically investigate how the tumor microenvironment in these high-risk cSCC differs from that of sporadic cSCC, highlight shared tumorigenic mechanisms, and identify knowledge gaps for future research. Specifically, we review immune cell infiltration, epithelial-mesenchymal transition, extracellular matrix remodeling, and related biomarkers, while also exploring potential therapeutic targets. It is surmised that both organ transplant recipients cSCC and recessive dystrophic epidermolysis bullosa cSCC may exhibit a permissive tumor microenvironment, potentially characterized by immune dysfunction and enhanced TGFβ signaling, contributing to tumor aggressiveness. Notably, organ transplant recipients cSCC primarily demonstrates immune exhaustion, whereas recessive dystrophic epidermolysis bullosa cSCC is driven by chronic tissue damage with concomitant extracellular matrix remodeling. A better understanding of tumor microenvironment features in these high-risk cSCC may help develop novel targeted therapies to improve patient outcomes.

Indexed as

Cutaneous squamous cell carcinomaEpidermolysis bullosaOrgan transplant recipientsTumor microenvironment

Identifiers

PMID41815791
PMCPMC12972515

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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.