Evidence map›Paper›PMID 29483830›Full record

ReviewInternational journal of biological sciences2018

The role of TGF-β/SMAD4 signaling in cancer.

Ming Zhao, Lopa Mishra, Chu-Xia Deng

Open access · goldAbstract readReview
In one paragraph

Review in International journal of biological sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 374 papers.

0numbers the graph read from it
0cells of the map it votes in
374citing papers in PubMed
19.8field-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

374 citing papers in PubMed, 609 citations in OpenAlex.

  1. Observational
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  17. Neo-Cysteine Molecular Glues for Targeting Mutated SMAD4 Protein.Angewandte Chemie (International ed. in English) · 2026
    Article
  18. Article
  19. Review
  20. Article

314 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

3 authors at 2 institutions in 2 countries.

Ming ZhaoFaculty of Health Sciences, University of Macau, Macau SAR, China.
Lopa MishraCenter for Translational Research, Department of Surgery and GW Cancer Center, George Washington University, Washington DC, USA.
Chu-Xia DengFaculty of Health Sciences, University of Macau, Macau SAR, China.
Affiliated Hospital of Southwest Medical University · CNUniversity of Macau · MO

Funding

Role of Beta Spectrin and Smad in Alcohol-Induced Liver and GI Cell ProliferationR01AA023146 · NIAAA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Lopa Mishra · 2013 to 2026
$4.6M
Cellular interactions between TGF-beta pathway members and epignetic regulators in liver and gastrointestinal cancersR01CA236591 · NCI · GEORGE WASHINGTON UNIVERSITY · PI Jian Chen, Lopa Mishra · 2018 to 2026
$3.0M
Molecular Mechanisms and Translational studies in Colon CancerI01BX003732 · VA · U.S. DEPT/VETS AFFAIRS MEDICAL CENTER · PI MISHRA, LOPA · 2017 to 2019
–
BLRD VA I01 BX003732NCI NIH HHS R01 CA236591NIAAA NIH HHS R01 AA023146
6 · The paper itself

Abstract

Transforming growth factor β (TGF-β) signaling pathway plays important roles in many biological processes, including cell growth, differentiation, apoptosis, migration, as well as cancer initiation and progression. SMAD4, which serves as the central mediator of TGF-β signaling, is specifically inactivated in over half of pancreatic duct adenocarcinoma, and varying degrees in many other types of cancers. In the past two decades, multiple studies have revealed that SMAD4 loss on its own does not initiate tumor formation, but can promote tumor progression initiated by other genes, such as KRAS activation in pancreatic duct adenocarcinoma and APC inactivation in colorectal cancer. In other cases, such as skin cancer, loss of SMAD4 plays an important initiating role by disrupting DNA damage response and repair mechanisms and enhance genomic instability, suggesting its distinct roles in different types of tumors. This review lists SMAD4 mutations in various types of cancer and summarizes recent advances on SMAD4 with focuses on the function, signaling pathway, and the possibility of SMAD4 as a prognostic indicator.

Indexed as

AnimalsDNA DamageDNA RepairEpithelial-Mesenchymal TransitionMiceModels, MolecularMutationNeoplasmsPrognosisSignal TransductionSmad4 ProteinTransforming Growth Factor betaSmad4 ProteinSmad4 protein, mouseTransforming Growth Factor betamouse modelprognosisSMAD4TGF-βtumorigenesis

Identifiers

PMID29483830
PMCPMC5821033
OpenAlexW2792793299

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.