Evidence map›Paper›PMID 40952278›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2025

Differences in Expression of Epithelial-Mesenchymal Transition (EMT) Induction Genes TGF-Β Pathway Transition in Colorectal Cancer Patients Non-Metastatic and Metastatic.

Ainul Mardiah, Hendra Susanto, Sri Rahayu Lestari, Moch Sholeh, Adeodatus Yuda Handaya, Arum Linangkung

Abstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

6 authors.

Ainul MardiahDepartment of Biology, Faculty of Science and Mathematics, Universitas Riau, Indonesia.
Hendra SusantoDepartment of Biology, Faculty of Mathematics and Natural Sciences, Universitas Negeri Malang, Malang, Indonesia.ORCID 0000-0002-3935-4848
Sri Rahayu LestariDepartment of Biology, Faculty of Mathematics and Natural Sciences, Universitas Negeri Malang, Malang, Indonesia.ORCID 0009-0006-9857-7781
Moch SholehDepartment of Biomedical Sciences, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.
Adeodatus Yuda HandayaDigestive Surgeon Division, Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Special Region of Yogyakarta, Indonesia.ORCID 0000000302561955
Arum LinangkungDigestive Surgeon Division, Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Special Region of Yogyakarta, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis research focuses on molecular screening of mRNA by targeting EMT regulator genes in the TGF-β/SMAD pathway to determine the difference in EMT mechanisms between non-metastatic and metastatic primary tumor cells.

methodsThe method uses Real time/quantitative Polymerase Chain Reaction (RT-qPCR) to measure the expression levels of target genes in colon tissue samples from non-metastatic and metastatic patient groups. Differences in target gene expression between the two groups were analyzed using t-tests.

resultsThe results of this study show significance differences in the expression of EMT-inducing genes on the TGF-β/Smad pathway between non-metastatic colorectal cancer groups and metastases. TGF-β1 (p-value : 0.041), Smad2 (p-value : 0.020), Snail1 (p-value : 0.028), Twist1 (p-value : 0.036), and ZEB1 (p-value : 0.045) gene expression was higher in the metastatic tumor group. In contrast to these genes, the expression of the Smad4 (p-value : 0.022), E-cadherin (p-value : 0.036), and vimentin (p-value : 0.048) genes was lower in the metastatic tumor group.

conclusionThe observed alterations in gene expression related to EMT within the TGF-β/Smad pathway in metastatic colorectal cancer are likely associated with the partial processes of EMT and MET. These alterations may contribute to further metastatic potential and increase the malignancy of the cancer.

Indexed as

Biomarkers, TumorColorectal NeoplasmsEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticTransforming Growth Factor betaTransforming Growth Factor beta1CadherinsFemaleFollow-Up StudiesHumansMaleMiddle AgedNeoplasm MetastasisNuclear ProteinsPrognosisSignal TransductionBiomarkers, TumorCadherinsNuclear ProteinsSmad2 ProteinSMAD2 protein, humanSmad4 ProteinSMAD4 protein, humanSNAI1 protein, humanSnail Family Transcription FactorsTransforming Growth Factor betaTransforming Growth Factor beta1TWIST1 protein, humanTwist-Related Protein 1VimentinZEB1 protein, humanZinc Finger E-box-Binding Homeobox 1colorectal cancerepithelial mesenchymal transitionMetastasisTGF-β /SMADTumor

Identifiers

PMID40952278
PMCPMC12862417

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LicenceCC BY-NC
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Registered trials

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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.