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Eurasian Journal of Medicine

                                                                                    and Oncology





                                        ORIGINAL RESEARCH ARTICLE
                                        Enhanced expression of metastasis-associated

                                        genes in colorectal cancer



                                                              1,2
                                        Adeodatus Yuda Handaya * , Hendra Susanto 3  , and Moch Sholeh 4
                                        1 Department of Surgery, Faculty of Medicine, Universitas Gadjah Mada, Yogyakarta, Indonesia
                                        2 Digestive Surgery Division, Sardjito Hospital, Yogyakarta, Indonesia
                                        3 Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Negeri Malang,
                                        Malang, East Java, Indonesia
                                        4 Department of Biomedical Sciences, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia




                                        Abstract
                                        Introduction: Globally, colorectal cancer (CRC) continues to be a major cause of
                                        cancer-related  morbidity  and  death,  with  metastasis—particularly  to  the  liver—
                                        significantly worsening patient outcomes.
                                        Objective: The aim of this study was to investigate the expression of key epithelial-
                                        mesenchymal transition (EMT) transcription factors (Snail family transcriptional
                                        repressor 1 [SNAI1], zinc finger e-box binding homeobox 1 [ZEB1], Slug, Twist, and
                                        metastasis-associated protein 3 [MTA3]) and the pro-inflammatory cytokine tumor
                                        necrosis factor-alpha (TNF-α) in CRC cases with and without metastasis to the liver.
                                        Methods: A total of 41 CRC patients (20 non-metastatic, 21 with liver metastasis)
                                        from Dr.  Sardjito General Hospital,  Yogyakarta, were examined utilizing reverse
            *Corresponding author:      transcription quantitative polymerase chain reaction of the adjacent normal tissues
            Adeodatus Yuda Handaya      and the tumors.
            (yudahandaya@ugm.ac.id)     Results:  SNAI1, ZEB1, Slug,  Twist, and  TNF-α were significantly upregulated in
            Citation: Handaya AY, Susanto H,   metastatic CRC, while MTA3 was downregulated. Expression of these markers
            Sholeh M. Enhanced expression   correlated with body mass index, liver enzymes (aspartate aminotransferase), and
            of metastasis-associated genes in   cancer stage.
            colorectal cancer. Eurasian J Med
            Oncol. 2025;9(3):250-260.   Conclusion: These findings highlight the central role of EMT-related transcription
            doi: 10.36922/EJMO025210202  factors and inflammatory signaling in CRC metastasis and suggest that targeting
            Received: May 19, 2025      these pathways could offer novel therapeutic strategies for metastatic CRC.
            Revised: June 23, 2025
                                        Keywords: Colorectal cancer; Liver metastasis; Body weight loss; Metastasis marker
            Accepted: July 23, 2025
            Published online: August 18, 2025
            Copyright: © 2025 Author(s).
            This is an Open-Access article   1. Introduction
            distributed under the terms of the
            Creative Commons Attribution   Colorectal cancer (CRC), the third most common malignancy and the second leading
            License, permitting distribution,   cause of cancer-related deaths worldwide, is one of the most common cancers.
                                                                                                             1
            and reproduction in any medium,
            provided the original work is   Incidence rates vary widely across different regions, with a higher prevalence observed
            properly cited.             in developed countries compared to developing countries. The etiology of CRC is
            Publisher’s Note: AccScience   multifactorial, involving a combination of genetic predispositions, lifestyle factors such
            Publishing remains neutral with   as diet and physical inactivity, and environmental influences. Notably, polymorphisms in
            regard to jurisdictional claims in
            published maps and institutional   several genes have been studied for their potential association with CRC risk, although
                                                                                    2-5
            affiliations.               findings regarding their significance have been mixed.  Pathologically, CRC typically

            Volume 9 Issue 3 (2025)                        250                         doi: 10.36922/EJMO025210202
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