Role of MTHFR gene polymorphisms, serum tissue inhibitor of metalloproteinases-1, thymus chemokine-1 and thrombospondin-1 in endometrial cancer

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The aim of this study was to evaluate the relationship between the MTHFR gene variants (677 C→T and 1298 A→C), serum tissue metalloproteinases inhibitor (TIMP-1), thrombospondin-1 (TSP-1), thymus chemokine-1 (TCK-1) levels and endometrial cancer. Sixty women were chosen from endometrial cancer patients and fifty-six women without any systemic disease were included as the control group. MTHFR C677T and A1298C MTHFR polymorphisms and their allele frequencies were evaluated with strip assay (Reverse hybridization method). Serum tissue inhibitor of metalloproteinases-1, thymus chemokine-1, and thrombospondin-1 levels were measured with the enzyme-linked immunosorbent assay (ELISA). Genotypic distribution and allelic frequencies of MTHFR C677T polymorphism were not associated with endometrial cancer (P > 0.05). But, genotypic distribution and allelic frequencies of MTHFR A1298C polymorphism were strongly associated with endometrial cancer (P = 0.047 and P = 0.024). On the other hand, tissue inhibitor of metalloproteinases-1, thrombospondin-1, and thymus chemokine-1 levels were strongly associated with endometrial cancer (P = 0.001, P = 0.02, and P = 0.001 respectively). These results indicate that genotypic distribution and allelic frequencies of MTHFR A1298C polymorphism, tissue inhibitor of metalloproteinases-1, thrombospondin-1 and thymus chemokine-1 may be the prognostic markers in endometrial carcinoma.

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AlanDeğerDil
dc.contributor.authorYildirim, Malik Ejder
dc.contributor.authorKiliçgün, Hasan
dc.contributor.authorKurtulgan, Hande Küçük
dc.contributor.authorKarakus, Savas
dc.contributor.authorErsan, Serpil
dc.contributor.authorBakir, Sevtap
dc.contributor.authorSezgin, Ilhan
dc.date.accessioned2026-10-18T20:29:59.542888639Z
dc.date.available2026-10-18T20:29:59.542888639Z
dc.date.issued2016
dc.description.abstractThe aim of this study was to evaluate the relationship between the MTHFR gene variants (677 C→T and 1298 A→C), serum tissue metalloproteinases inhibitor (TIMP-1), thrombospondin-1 (TSP-1), thymus chemokine-1 (TCK-1) levels and endometrial cancer. Sixty women were chosen from endometrial cancer patients and fifty-six women without any systemic disease were included as the control group. MTHFR C677T and A1298C MTHFR polymorphisms and their allele frequencies were evaluated with strip assay (Reverse hybridization method). Serum tissue inhibitor of metalloproteinases-1, thymus chemokine-1, and thrombospondin-1 levels were measured with the enzyme-linked immunosorbent assay (ELISA). Genotypic distribution and allelic frequencies of MTHFR C677T polymorphism were not associated with endometrial cancer (P > 0.05). But, genotypic distribution and allelic frequencies of MTHFR A1298C polymorphism were strongly associated with endometrial cancer (P = 0.047 and P = 0.024). On the other hand, tissue inhibitor of metalloproteinases-1, thrombospondin-1, and thymus chemokine-1 levels were strongly associated with endometrial cancer (P = 0.001, P = 0.02, and P = 0.001 respectively). These results indicate that genotypic distribution and allelic frequencies of MTHFR A1298C polymorphism, tissue inhibitor of metalloproteinases-1, thrombospondin-1 and thymus chemokine-1 may be the prognostic markers in endometrial carcinoma.
dc.identifier.endpage10750
dc.identifier.issn1936-2625
dc.identifier.issue10
dc.identifier.scopus2-s2.0-84994336303
dc.identifier.startpage10746
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15205
dc.identifier.volume9
dc.language.isoen
dc.publisherE-Century Publishing Corporation
dc.relation.ispartofInternational Journal of Clinical and Experimental Pathology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectEndometrial cancer
dc.subjectGene polymorphisms
dc.subjectMTHFR C677T A1298C
dc.subjectTCK-1
dc.subjectTIMP-1
dc.subjectTSP-1
dc.titleRole of MTHFR gene polymorphisms, serum tissue inhibitor of metalloproteinases-1, thymus chemokine-1 and thrombospondin-1 in endometrial cancer
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus0
rdl.source.indexSCOPUS