Evidence map›Paper›PMID 40390959›Full record

ArticleJournal of obstetrics and gynaecology of India2025

Prevalence of Mismatch Repair Gene Defects by Means of Immuno-histochemistry Staining for MMR Proteins in Endometrial Cancer.

Kaustubh Girish Burde, Indu R Nair, Pavithran Keechilattu, Anupama Rajanbabu

Abstract read
In one paragraph

Article in Journal of obstetrics and gynaecology of India, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kaustubh Girish BurdeDepartment of Gynaecological Oncology, Amrita Institute of Medical Sciences, Kochi, Kerala 682024 India.
Indu R NairDepartment of Pathology, Amrita Institute of Medical Sciences, Kochi, Kerala 682024 India.
Pavithran KeechilattuDepartment of Medical Oncology, Amrita Institute of Medical Sciences, Kochi, Kerala 682024 India.
Anupama RajanbabuDepartment of Gynaecological Oncology, Amrita Institute of Medical Sciences, Kochi, Kerala 682024 India.ORCID 0000-0002-2885-8098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: In India, the incidence of uterine cancer is 17,420 per year. Presence of mismatch repair genes is one of the risk factors which can cause microsatellite instability in DNA leading to hereditary syndromes as well as sporadic cancer. In the present study, we aim to determine the prevalence of MMR gene mutations by IHC staining for MMR proteins in endometrial cancer. We further aim to corelate various clinic-pathological features with mismatch repair gene defect (MMRd) cancers and to determine its effects recurrence and survival in endometrial cancer. Materials and Methods: This is an ambispective study of a retrospectively selected cohort followed up prospectively. It was conducted in the Department of Gynaecological Oncology, AIMS. The cohort was evaluated for the four MMR proteins via IHC staining, and their various clinic-pathological factors were studied. Also, the factors affecting their recurrence free survival (RFS) and overall survival (OS) were observed. Results: The prevalence of MMR loss in endometrial cancer patients was 31.34%. Most common loss of MMR gene was MLH1 and PMS 2 (57.14%). We did not find any significant differences pertaining to age, BMI, menstrual status, family history and second malignancies in both groups of endometrial cancers. While comparing the histopathological characteristics, no significant difference was found regarding to histopathology, stage, type, grade, P53 status, tumour size, lymph node involvement and LVSI status. No significant difference was seen between two groups in RFS and OS. Conclusion: We found a significant proportion of endometrial cancers with defective MMR genes in Indian population. We did not find any correlation of MMR to the various clinical and histopathological factors that we analysed. MMRd did not significantly affect the RFS and OS in endometrial cancers.

Indexed as

Endometrial cancerMismatch repair proteinsMMR gene defectMolecular classification of uterine cancerUterine cancer

Identifiers

PMID40390959
PMCPMC12085453

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.