Evidence map›Paper›PMID 37327314›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2023

Activin A-Mediated Polarization of Cancer-Associated Fibroblasts and Macrophages Confers Resistance to Checkpoint Immunotherapy in Skin Cancer.

Christine Pich-Bavastro, Laura Yerly, Jeremy Di Domizio, Stéphanie Tissot-Renaud, Michel Gilliet, François Kuonen

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05933954 (Double-blind Randomized Controlled Study of the Effects of 5G Radiation on Skin), which is not on this map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
6.2field-weighted citation impact, top 3% of its field
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.

NCT05933954 narecruitingnot on this mapstarted 2024, after this paper: background citation

Double-blind Randomized Controlled Study of the Effects of 5G Radiation on Skin

TypeinterventionalSponsorProf. Olivier Gaide, MD-PhDRan2024 to 2026Enrolled42ConditionsElectromagnetic Radiation (5GFR2)Arms5GFR2 non ionizing EMW exposure
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 27 citations in OpenAlex.

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  13. Targeting LINC01711 in FAPCell death & disease · 2025
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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 at 2 institutions in 1 country.

Christine Pich-BavastroDepartment of Dermatology and Venereology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.ORCID 0000-0002-6526-749X
Laura YerlyDepartment of Dermatology and Venereology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.ORCID 0000-0003-2663-8101
Jeremy Di DomizioDepartment of Dermatology and Venereology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.ORCID 0000-0002-6281-3918
Stéphanie Tissot-RenaudDepartment of Oncology, Immune Landscape Laboratory, Center of Experimental Therapeutics, Lausanne University Hospital, Lausanne, Switzerland.ORCID 0000-0003-3080-4598
Michel GillietDepartment of Dermatology and Venereology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.ORCID 0000-0002-4609-3762
François KuonenDepartment of Dermatology and Venereology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.ORCID 0000-0001-6137-7483
University of Lausanne · CHLudwig Cancer Research · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCemiplimab is approved for the treatment of locally advanced basal cell carcinomas (BCC), although with mitigated results. We sought to interrogate the cellular and molecular transcriptional reprogramming underlying BCC resistance to immunotherapy. EXPERIMENTAL

designHere, we combined spatial and single-cell transcriptomics to deconvolute the spatial heterogeneity of the tumor microenvironment in regard with response to immunotherapy, in a cohort of both naïve and resistant BCCs.

resultsWe identified subsets of intermingled cancer-associated fibroblasts (CAF) and macrophages contributing the most to CD8 T-cell exclusion and immunosuppression. Within this spatially resolved peritumoral immunosuppressive niche, CAFs and adjacent macrophages were found to display Activin A-mediated transcriptional reprogramming towards extracellular matrix remodeling, suggesting active participation to CD8 T-cell exclusion. In independent datasets of human skin cancers, Activin A-conditioned CAFs and macrophages were associated with resistance to immune checkpoint inhibitors (ICI).

conclusionsAltogether, our data identify the cellular and molecular plasticity of tumor microenvironment (TME) and the pivotal role of Activin A in polarizing the TME towards immune suppression and ICI resistance.

Indexed as

Basal Cell CarcinomaCancer-Associated FibroblastsSkin NeoplasmsActivinsHumansImmunotherapyMacrophagesTumor Microenvironmentactivin AActivins

Identifiers

PMID37327314
PMCPMC10472111
OpenAlexW4380989503

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.