Evidence map›Paper›PMID 34209646›Full record

ReviewCancers2021

The TGF-β Pathway: A Pharmacological Target in Hepatocellular Carcinoma?

Ester Gonzalez-Sanchez, Javier Vaquero, Maite G Férnandez-Barrena, Juan José Lasarte, Matías A Avila, Pablo Sarobe, María Reig, Mariona Calvo, Isabel Fabregat

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
4.9field-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.

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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 89 citations in OpenAlex.

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  14. New Experimental Mouse Models to Evaluate the Role of Transforming Growth Factor-Beta in Liver Tumorigenesis.Liver international : official journal of the International Association for the Study of the Liver · 2025
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12 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 1 country.

Ester Gonzalez-SanchezCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), National Biomedical Research Institute on Liver and Gastrointestinal Diseases, Instituto de Salud Carlos III, 28029 Madrid, Spain.
Javier VaqueroCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), National Biomedical Research Institute on Liver and Gastrointestinal Diseases, Instituto de Salud Carlos III, 28029 Madrid, Spain.ORCID 0000-0002-6020-6962
Maite G Férnandez-BarrenaCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), National Biomedical Research Institute on Liver and Gastrointestinal Diseases, Instituto de Salud Carlos III, 28029 Madrid, Spain.ORCID 0000-0003-0375-6236
Juan José LasarteInstituto de Investigaciones Sanitarias de Navarra IdiSNA, 31008 Pamplona, Spain.ORCID 0000-0003-1641-3881
Matías A AvilaCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), National Biomedical Research Institute on Liver and Gastrointestinal Diseases, Instituto de Salud Carlos III, 28029 Madrid, Spain.ORCID 0000-0001-6570-3557
Pablo SarobeCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), National Biomedical Research Institute on Liver and Gastrointestinal Diseases, Instituto de Salud Carlos III, 28029 Madrid, Spain.
María ReigCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), National Biomedical Research Institute on Liver and Gastrointestinal Diseases, Instituto de Salud Carlos III, 28029 Madrid, Spain.ORCID 0000-0002-5711-9534
Mariona CalvoBellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, 08908 Barcelona, Spain.
Isabel FabregatCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), National Biomedical Research Institute on Liver and Gastrointestinal Diseases, Instituto de Salud Carlos III, 28029 Madrid, Spain.ORCID 0000-0003-0136-8440
Instituto de Salud Carlos III · ESInstitut d'Investigació Biomédica de Bellvitge · ESNavarre Institute of Health Research · ES

Funding

Agencia Estatal de Investigación RYC2018-024475-1Agencia Estatal de Investigación SAF2017-88933-R, RTI2018-094079-B-100, PID2019-108651RJ-I00/DOI: 10.13039/501100011033, PID2019-108989RB-I00 and PID2019-104878RB-100/AEI/10.13039/50110001103Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas CB06/04/0006, CB06/04/0005, CB17/04/00017 and Emergent Investigators' Program grantFundación Científica Asociación Española Contra el Cáncer Not ApplicableInstituto de Salud Carlos III PI17/00249 and FIS18/00358Murchante contra el cáncer" initiative Not Applicable
6 · The paper itself

Abstract

Transforming Growth Factor-beta (TGF-β) superfamily members are essential for tissue homeostasis and consequently, dysregulation of their signaling pathways contributes to the development of human diseases. In the liver, TGF-β signaling participates in all the stages of disease progression from initial liver injury to hepatocellular carcinoma (HCC). During liver carcinogenesis, TGF-β plays a dual role on the malignant cell, behaving as a suppressor factor at early stages, but contributing to later tumor progression once cells escape from its cytostatic effects. Moreover, TGF-β can modulate the response of the cells forming the tumor microenvironment that may also contribute to HCC progression, and drive immune evasion of cancer cells. Thus, targeting the TGF-β pathway may constitute an effective therapeutic option for HCC treatment. However, it is crucial to identify biomarkers that allow to predict the response of the tumors and appropriately select the patients that could benefit from TGF-β inhibitory therapies. Here we review the functions of TGF-β on HCC malignant and tumor microenvironment cells, and the current strategies targeting TGF-β signaling for cancer therapy. We also summarize the clinical impact of TGF-β inhibitors in HCC patients and provide a perspective on its future use alone or in combinatorial strategies for HCC treatment.

Indexed as

HCCHCC immunotherapyHCC targeted therapyTGF-betaTGF-beta inhibitors

Identifiers

PMID34209646
PMCPMC8268320
OpenAlexW3174859635

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.