Evidence map›Paper›PMID 39164192›Full record

ReviewCancer biology & therapy2024

Exploring the molecular mechanisms and therapeutic potential of SMAD4 in colorectal cancer.

Hui Shan, Guangyu Tian, Yeqing Zhang, Zhiyuan Qiu

Abstract readReview
In one paragraph

Review in Cancer biology & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. 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

4 authors.

Hui ShanDepartment of Oncology, the Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Guangyu TianDepartment of Oncology, Jiangdu People's Hospital Affiliated to Yangzhou University, Yangzhou, Jiangsu, China.
Yeqing ZhangDepartment of Vascular Surgery, the Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Zhiyuan QiuDepartment of Oncology, the Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.ORCID 0000-0002-8782-6758

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal Cancer (CRC) is the third most common cancer worldwide, and the occurrence and development of CRC are influenced by the molecular biology characteristics of CRC, especially alterations in key signaling pathways. The transforming growth factor-β (TGF-β) plays a crucial role in cellular growth, differentiation, migration, and apoptosis, with SMAD4 protein serving as a key transcription factor in the TGF-β signaling pathway, thus playing a significant role in the onset and progression of CRC. CRC is one of the malignancies with a high mortality rate worldwide. Despite significant research progress in recent years, especially regarding the role of SMAD4, its dual role in the early and late stages of tumor progression has promoted further discussion on its complexity as a therapeutic target, highlighting the urgent need for a deeper analysis of its role in CRC. This review aims to explore the function of SMAD4 protein in CRC and its potential as a therapeutic target.

Indexed as

Colorectal NeoplasmsSmad4 ProteinAnimalsGene Expression Regulation, NeoplasticHumansSignal TransductionTransforming Growth Factor betaSmad4 ProteinSMAD4 protein, humanTransforming Growth Factor betaCRCSMAD4 proteinTgf-β pathway

Identifiers

PMID39164192
PMCPMC11340766

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.