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Association of Clinicopathological Factors With MMP13 (rs2252070) Gene Polymorphism in Swedish Patients With Colorectal Cancer
Department of Medical Laboratory, Danang University of Medical Technology and Pharmacy, Danang, Viet Nam.
Department of Laboratory Medicine and Pathology, Region Jönköping County, Jönköping, Sweden.
Department of Surgery, Region Jönköping County, Jönköping, Sweden; Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
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2024 (English)In: In Vivo, ISSN 0258-851X, E-ISSN 1791-7549, Vol. 38, no 4, p. 1775-1782Article in journal (Refereed) Published
Abstract [en]

Background/Aim: Matrix metalloproteinase 13 (MMP13) has been reported to be involved in tumor development and progression, including of colorectal cancer (CRC). This study aimed at evaluating whether the MMP13 rs2252070 gene polymorphism is associated with clinicopathological factors and its influence on long-term survival in Swedish patients with CRC.

Patients and Methods: A total of 723 patients with CRC were genotyped using TaqMan single nucleotide polymorphism assays based on polymerase chain reaction.

Results: Assessing clinicopathological factors, we demonstrated that having the G/G genotype for MMP13 rs2252070 was significantly associated with poor differentiation, higher serum level of carcinoembryonic antigen and higher lymph node status. Moreover, the presence of a G allele was significantly related to larger tumor size in rectal cancer but had a significantly protective role against mucinous cancer, perineural invasion and lymphovascular invasion. Kaplan-Meier analysis showed no difference between genotypes regarding cancer-specific survival.

Conclusion: Our findings highlight the potential of MMP13 rs2252070 polymorphism as a useful predictor of poor differentiation, serum level of carcinoembryonic antigen, lymph node status, tumor size, mucinous cancer, perineural invasion and lymphovascular invasion in patients with CRC. 

Place, publisher, year, edition, pages
International Institute of Anticancer Research, 2024. Vol. 38, no 4, p. 1775-1782
Keywords [en]
clinical parameters, colorectal cancer, MMP13, SNP, Adult, Aged, Aged, 80 and over, Alleles, Biomarkers, Tumor, Carcinoembryonic Antigen, Colorectal Neoplasms, Female, Genetic Association Studies, Genetic Predisposition to Disease, Genotype, Humans, Kaplan-Meier Estimate, Male, Matrix Metalloproteinase 13, Middle Aged, Neoplasm Staging, Polymorphism, Single Nucleotide, Prognosis, Sweden, collagenase 3, MMP13 protein, human, tumor marker, allele, antigen blood level, Article, cancer patient, cancer prevention, cancer specific survival, clinical feature, colorectal adenocarcinoma, controlled study, DNA polymorphism, follow up, genetic association, genotyping, histopathology, human, human tissue, long term survival, lymph node, lymph vessel metastasis, major clinical study, perineural invasion, polymerase chain reaction, single nucleotide polymorphism, Swedish citizen, tumor differentiation, tumor volume, very elderly, blood, cancer staging, colorectal tumor, epidemiology, genetic association study, genetic predisposition, genetics, Kaplan Meier method, mortality, pathology
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Cancer and Oncology
Identifiers
URN: urn:nbn:se:hj:diva-65694DOI: 10.21873/invivo.13628ISI: 001266321000027PubMedID: 38936942Scopus ID: 2-s2.0-85197118136Local ID: GOA;;963051OAI: oai:DiVA.org:hj-65694DiVA, id: diva2:1884720
Funder
Futurum - Academy for Health and Care, Jönköping County Council, Sweden, Futurum-970572, Futurum-989025Available from: 2024-07-18 Created: 2024-07-18 Last updated: 2024-07-22Bibliographically approved

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Dimberg, Jan

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