Evidence map›Paper›PMID 40469190›Full record

ReviewFrontiers in oncology2025

Role of TGFβ-activated cancer-associated fibroblasts in the resistance to checkpoint blockade immunotherapy.

Weibin Hou

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
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  5. Advances in Immunotherapy for Intrahepatic Cholangiocarcinoma.International journal of molecular sciences · 2026
    Review
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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

1 author.

Weibin HouDepartment of Urology, the Third Xiangya Hospital, Central South University, Changsha, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint blockers (ICBs) have revolutionized cancer treatment by enabling durable responses. However, most patients showed resistance and limited efficacy. Elucidating mechanisms of resistance is imperative to extend the clinical utility of ICBs. Emerging evidence highlights cancer-associated fibroblasts (CAFs), particularly TGFβ-activated myofibroblastic CAFs, as key orchestrators of immunosuppressive TMEs and ICBs resistance. These CAFs drive T-cell exclusion preventing intratumoral T cells from engaging cancer cells. This review explores the role of TGFβ signaling in CAFs in driving immune evasion and therapy resistance. While targeting TGFβ or CAFs directly has shown limited inconsistent results, downstream molecules in TGFβ-activated CAFs, including induced TGFβ (βig-h3), endocytic receptor 180 (Endo180), leucine-rich repeat containing 15 (LRRC15), and NADPH oxidase 4 (NOX4), emerge as promising therapeutic targets to counteract T-cell exclusion and restore immunotherapy sensitivity. Advancing research on CAF heterogeneity and pro-tumorigenic subsets may uncover innovative strategies to expand immunotherapy benefits.

Indexed as

cancer associated fibroblasts (CAFs)immune checkpoint blockers (ICBs)immunotherapy resistancemyofibroblastT cell exclusiontransforming growth factor beta (TGFβ)

Identifiers

PMID40469190
PMCPMC12133491

What OpenQuestion holds

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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.