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

Mardiah, Ainul and Susanto, Hendra and Lestari, Sri Rahayu and Sholeh, Moch and Handaya, Adeodatus Yuda and Linangkung, Arum (2025) Differences in Expression of Epithelial-Mesenchymal Transition (EMT) Induction Genes TGF-B Pathway Transition in Colorectal Cancer Patients Non-Metastatic and Metastatic. Asian Pacific Journal of Cancer Prevention, 26 (9). 3239 - 3245. ISSN 15137368

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Abstract

This 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. The 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. The 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. The 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. © This work is licensed under a Creative Commons Attribution-Non Commercial 4.0 International License.

Item Type: Article
Additional Information: Cited by: 2; All Open Access; Gold Open Access
Uncontrolled Keywords: Biomarkers, Tumor; Cadherins; Colorectal Neoplasms; Epithelial-Mesenchymal Transition; Female; Follow-Up Studies; Gene Expression Regulation, Neoplastic; Humans; Male; Middle Aged; Neoplasm Metastasis; Nuclear Proteins; Prognosis; Signal Transduction; Smad2 Protein; Smad4 Protein; Snail Family Transcription Factors; Transforming Growth Factor beta; Transforming Growth Factor beta1; Twist-Related Protein 1; Vimentin; Zinc Finger E-box-Binding Homeobox 1; cadherin; nuclear protein; Smad2 protein; SMAD2 protein, human; Smad4 protein; SMAD4 protein, human; SNAI1 protein, human; transcription factor Snail; transcription factor ZEB1; transforming growth factor beta; transforming growth factor beta1; tumor marker; Twist related protein 1; TWIST1 protein, human; vimentin; ZEB1 protein, human; colorectal tumor; epithelial mesenchymal transition; female; follow up; gene expression regulation; genetics; human; male; metabolism; metastasis; middle aged; pathology; prognosis; signal transduction
Subjects: R Medicine > RD Surgical Divisions
Divisions: Faculty of Medicine, Public Health and Nursing > Surgical Divisions
Depositing User: Ani PURWANDARI
Date Deposited: 13 Aug 2026 08:30
Last Modified: 13 Aug 2026 08:30
URI: https://ir.lib.ugm.ac.id/id/eprint/28692

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