Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/33738
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dc.contributor.authorJoksimovic, Marijaen_US
dc.contributor.authorJankulovski, Nikolaen_US
dc.contributor.authorPetrushevska, Gordanaen_US
dc.contributor.authorOgnenoska Jankovska, Biljanaen_US
dc.contributor.authorZafirova Ivanovska, Betien_US
dc.contributor.authorStojcevski, Sashoen_US
dc.contributor.authorAluloski, Igoren_US
dc.contributor.authorTanturovski, Mileen_US
dc.contributor.authorJoksimovic, Vladimiren_US
dc.date.accessioned2025-07-07T09:11:06Z-
dc.date.available2025-07-07T09:11:06Z-
dc.date.issued2024-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/33738-
dc.description.abstractBackground: This study examines the relationship between mismatch repair (MMR) gene expression and clinicopathological features in patients with low-grade endometrial cancer (EC). Methods: A prospective cohort of 40 patients with histologically confirmed low-grade EC underwent immunohistochemical analysis to determine MMR status. Clinical data, including age, body mass index (BMI), menopausal status, parity, and comorbidities, were collected. Histopathological evaluations assessed myometrial invasion,lymphovascular invasion and disease stage. Results: MMR deficiency (MMRd) was identified in 35% of patients, predominantly associated with MLH1/PMS2 loss. No significant associations were found between MMR status and clinical characteristics such as age, BMI, or comorbidities. However, MMRd tumors exhibited a significantly higher prevalence of myometrial invasion over 50% (85.71% vs. 38.46%, p=0.0042) and lymphovascular invasion (71.43% vs. 19.23%, p=0.00114). Additionally, MMRd cases were more frequently associated with advanced disease stages, particularly in stage IIIC (28.57% vs. 7.69%, p=0.078). Conclusion: The importance of MMR status in the biological behavior of low-grade endometrial cancer is highlighted in this study. The strong correlation between MMR deficiency and aggressive histopathological features such as increased myometrial and lymphovascular invasion, highlights the need to integrate MMR testing into clinical practice, even if clinical parameters showed no significant association with MMR expression. These results suggest that MMRd may be a useful prognostic indicator that requires more research to improve patient outcomes and treatment approaches for low-grade endometrial cancer.en_US
dc.language.isoenen_US
dc.publisherMacedonian Association of Anatomists and Morphologistsen_US
dc.relation.ispartofJournal of Morphological Sciencesen_US
dc.subjectendometrial canceren_US
dc.subjectlow gradeen_US
dc.subjectmismatch repairen_US
dc.titleRELATIONSHIP OF IMMUNOHISTOCHEMICAL EXPRESSION OF MISMATCH REPAIR GENE PRODUCTS AND CLINICOPATHOLOGICAL FEATURES IN PATIENTS WITH LOW-GRADE ENDOMETRIAL CANCERen_US
dc.typeArticleen_US
dc.identifier.doi10.55302/jms2473016j-
dc.identifier.volume7-
dc.identifier.issue3-
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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