Evidence map›Paper›PMID 35295334›Full record

ReviewFrontiers in pharmacology2022

Transforming Growth Factor-Beta (TGF-β) Signaling in Cancer-A Betrayal Within.

Abdul Basit Baba, Bilal Rah, Gh Rasool Bhat, Ifra Mushtaq, Sabra Parveen, Rukhsana Hassan, Mahrukh Hameed Zargar, Dil Afroze

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed
16.7field-weighted citation impact, top 1% 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

124 citing papers in PubMed, 207 citations in OpenAlex.

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  12. SMURF2 in Anticancer Therapy: Dual Role in Carcinogenesis and Theranostics.International journal of molecular sciences · 2026
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64 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

8 authors at 1 institution in 1 country.

Abdul Basit BabaAdvanced Centre for Human Genetics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.
Bilal RahAdvanced Centre for Human Genetics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.
Gh Rasool BhatAdvanced Centre for Human Genetics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.
Ifra MushtaqAdvanced Centre for Human Genetics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.
Sabra ParveenAdvanced Centre for Human Genetics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.
Rukhsana HassanAdvanced Centre for Human Genetics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.
Mahrukh Hameed ZargarAdvanced Centre for Human Genetics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.
Dil AfrozeAdvanced Centre for Human Genetics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.
Sher-i-Kashmir Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A ubiquitously expressed cytokine, transforming growth factor-beta (TGF-β) plays a significant role in various ongoing cellular mechanisms. The gain or loss-of-function of TGF-β and its downstream mediators could lead to a plethora of diseases includes tumorigenesis. Specifically, at the early onset of malignancy TGF-β act as tumour suppressor and plays a key role in clearing malignant cells by reducing the cellular proliferation and differentiation thus triggers the process of apoptosis. Subsequently, TGF-β at an advanced stage of malignancy promotes tumorigenesis by augmenting cellular transformation, epithelial-mesenchymal-transition invasion, and metastasis. Besides playing the dual roles, depending upon the stage of malignancy, TGF-β also regulates cell fate through immune and stroma components. This oscillatory role of TGF-β to fight against cancer or act as a traitor to collaborate and crosstalk with other tumorigenic signaling pathways and its betrayal within the cell depends upon the cellular context. Therefore, the current review highlights and understands the dual role of TGF-β under different cellular conditions and its crosstalk with other signaling pathways in modulating cell fate.

Indexed as

metastasissignaling pathwaysTGF-β 1tumorigenesistumor suppressor

Identifiers

PMID35295334
PMCPMC8918694
OpenAlexW4214590743

What Socratic 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 Socratic graph.