Evidence map›Paper›PMID 39989503›Full record

ReviewOncoTargets and therapy2025

Exploring TGF-β Signaling in Cancer Progression: Prospects and Therapeutic Strategies.

Khansa Ali Sheikh, Momna Amjad, Mahnoor Tabassum Irfan, Sumaira Anjum, Tanveer Majeed, Muhammad Usman Riaz, Amar Yasser Jassim, Elham Abdullatif M Sharif, Wisam Nabeel Ibrahim

Abstract readReview
In one paragraph

Review in OncoTargets and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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  8. Synthesis and Anticancer Activity of New Quinazolin-4(3Pharmaceuticals (Basel, Switzerland) · 2026
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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

9 authors.

Khansa Ali Sheikh *Department of Biotechnology, Kinnaird College for Women, Lahore, Pakistan.
Momna Amjad *Department of Biotechnology, Kinnaird College for Women, Lahore, Pakistan.ORCID 0009-0007-5206-972X
Mahnoor Tabassum Irfan *Department of Biotechnology, Kinnaird College for Women, Lahore, Pakistan.
Sumaira AnjumDepartment of Biotechnology, Kinnaird College for Women, Lahore, Pakistan.ORCID 0000-0003-2276-8785
Tanveer MajeedDepartment of Biotechnology, Kinnaird College for Women, Lahore, Pakistan.
Muhammad Usman RiazSchool of Computer Science, University College Dublin, Belfield, Dublin 4, Ireland.ORCID 0000-0002-4325-3468
Amar Yasser JassimMarine Science Center, University of Basrah, Basrah, Iraq.ORCID 0000-0002-4938-2156
Elham Abdullatif M SharifDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha, Qatar.ORCID 0000-0001-8463-8893
Wisam Nabeel IbrahimDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha, Qatar.ORCID 0000-0001-6008-1947

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer persists as a ubiquitous global challenge despite the remarkable advances. It is caused by uncontrolled cell growth and metastasis. The Transforming Growth Factor-beta (TGF-β) signaling pathway is considered a primary regulator of various normal physiological processes in the human body. Recently, factors determining the nature of TGF-β response have received attention, specifically its signaling pathway which can be an attractive therapeutic target for various cancer treatments. The TGF-β receptor is activated by its ligands and undergoes transduction of signals via canonical (SMAD dependent) or non-canonical (SMAD independent) signaling pathways regulating several cellular functions. Furthermore, the cross talk of the TGF-β signaling pathway cross with other signaling pathways has shown the controlled regulation of cellular functions. This review highlights the cross talk between various major signaling pathways and TGF-β. These signaling pathways include Wnt, NF-κB, PI3K/Akt, and Hedgehog (Hh). TGF-β signaling pathway has a dual role at different stages. It can suppress tumor formation at early stages and promote progression at advanced stages. This complex behaviour of TGF-β has made it a promising target for therapeutic interventions. Moreover, many strategies have been designed to control TGF-β signaling pathways at different levels, inhibiting tumor-promoting while enhancing tumor-suppressive effects, each with unique molecular mechanisms and clinical implications. This review also discusses various therapeutic inhibitors including ligand traps, small molecule inhibitors (SMIs), monoclonal antibodies (mAbs), and antisense oligonucleotides which target specific components of TGF-β signaling pathway to inhibit TGF-β signaling and are studied in both preclinical and clinical trials for different types of cancer. The review also highlights the prospect of TGF-β signaling in normal physiology and in the case of dysregulation, TGF-β inhibitors, and different therapeutic effects in cancer therapy along with the perspective of combinational therapies to treat cancer.

Indexed as

cancercanonical signaling pathwaycombinational therapiesHedgehogtransforming growth factor betatumor promotingtumor suppression

Identifiers

PMID39989503
PMCPMC11846535

What OpenQuestion holds

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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.