Evidence map›Paper›PMID 41395640›Full record

ReviewHistopathology2026

RB1 inactivation in cutaneous carcinomas.

Tiffany Liv, Antoine Touzé, David Schrama, Serge Guyétant, Mahtab Samimi, Michael T Tetzlaff, Benjamin A Wood, Paul W Harms, Thibault Kervarrec

Abstract readReview
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Tiffany LivÉquipe Biologie des Infections à Polyomavirus, UMR INRAE ISP 1282, Université de Tours, Tours, France.ORCID https://orcid.org/0009-0009-9575-2347
Antoine TouzéÉquipe Biologie des Infections à Polyomavirus, UMR INRAE ISP 1282, Université de Tours, Tours, France.ORCID https://orcid.org/0000-0002-9856-9945
David SchramaDepartments of Dermatology, Venereology and Allergology, University Hospital Würzburg, Würzburg, Germany.ORCID https://orcid.org/0000-0002-6931-8194
Serge GuyétantÉquipe Biologie des Infections à Polyomavirus, UMR INRAE ISP 1282, Université de Tours, Tours, France.ORCID https://orcid.org/0000-0003-2783-9722
Mahtab SamimiÉquipe Biologie des Infections à Polyomavirus, UMR INRAE ISP 1282, Université de Tours, Tours, France.ORCID https://orcid.org/0000-0001-6742-9088
Michael T TetzlaffDepartment of pathology, University of California, San Francisco, California, USA.ORCID https://orcid.org/0000-0001-7899-4138
Benjamin A WoodDermatopathology Group, PathWest Laboratory Medicine, Perth, Western Australia, Australia.ORCID https://orcid.org/0000-0003-4977-3410
Paul W HarmsDepartments of Dermatology and Pathology, University of Michigan, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0002-0802-2883
Thibault KervarrecÉquipe Biologie des Infections à Polyomavirus, UMR INRAE ISP 1282, Université de Tours, Tours, France.ORCID https://orcid.org/0000-0002-2201-6914

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RB1 was the first identified tumour suppressor gene, named for its crucial role in opposing retinoblastoma oncogenesis. The RB1 gene encodes the retinoblastoma protein pRB, which is a well-known negative regulator of the cell cycle. However, pRB also contributes to cell differentiation by restricting reprogramming and stem cell properties. Accordingly, RB1 inactivation in tumours can induce phenotypic modifications, contributing to tumour progression. Indeed, RB1 pathogenic alterations, either point mutations or deletions, leading to pRB loss of function are observed in 5% of all human cancers. Mutations are much more prevalent in some histologic subgroups, including retinoblastoma, spindle cell lipoma, neuroendocrine prostate cancer and small cell lung carcinoma. In such entities, molecular investigation of tumour samples and mechanistic studies strongly suggest that early RB1 inactivation contributes not only to dysregulation of cell cycle control, but also to the tumour cell phenotype. Among skin carcinomas, RB1 inactivation is the hallmark of primary cutaneous neuroendocrine carcinoma commonly known as Merkel cell carcinoma (MCC), but it has also been described in other tumours including a subset of squamous cell carcinomas, sebaceous carcinomas and the recently described Wnt/beta-catenin-activated non-pilomatrical carcinomas. In this context, we provide a brief overview of the contribution of RB1 inactivation to oncogenesis and tumour cell phenotypes in general and summarise current knowledge regarding RB1-deficient cutaneous carcinomas, highlighting the potential uses of RB1 pathway characterisation for diagnosis, prognosis and therapeutic purposes.

Indexed as

Retinoblastoma Binding ProteinsRetinoblastoma ProteinSkin NeoplasmsUbiquitin-Protein LigasesCarcinoma, Merkel CellCarcinoma, NeuroendocrineHumansRB1 protein, humanRetinoblastoma Binding ProteinsRetinoblastoma ProteinUbiquitin-Protein LigasesMerkel cell carcinomaRB1sebaceous carcinomasquamous cell carcinomaWnt/beta‐catenin non pilomatrical carcinoma

Identifiers

PMID41395640
PMCPMC12891924

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.