Evidence map›Paper›PMID 40748292›Full record

ArticleTurk patoloji dergisi2025

Comparative Analysis of Next-Generation Sequencing and Immunohistochemistry in MSI/MMR Testing.

Cisel Aydin Mericoz, Zeynep Secil Satilmis, Fatma Esrefi, Gulsum Caylak, Burcu Saka, Ayse Armutlu, Orhun Cig Taskin, Ibrahim Kulac

Abstract readComparative Study
In one paragraph

Article in Turk patoloji dergisi, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Cisel Aydin MericozDepartment of Pathology, School of Medicine, Koç University, ISTANBUL, TURKEY.
Zeynep Secil SatilmisKoç University Hospital, ISTANBUL, TÜRKİYE.
Fatma EsrefiDepartment of Pathology, School of Medicine, Koç University, ISTANBUL, TURKEY.
Gulsum CaylakKoç University Hospital, ISTANBUL, TÜRKİYE.
Burcu SakaDepartment of Pathology, School of Medicine, Koç University, ISTANBUL, TURKEY.
Ayse ArmutluDepartment of Pathology, School of Medicine, Koç University, ISTANBUL, TURKEY.
Orhun Cig TaskinDepartment of Pathology, School of Medicine, Koç University, ISTANBUL, TURKEY.
Ibrahim KulacDepartment of Pathology, School of Medicine, Koç University, ISTANBUL, TURKEY.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveLoss of mismatch repair (MMR) protein expression, assessed via immunohistochemistry (IHC), and microsatellite instability (MSI) status, determined through molecular methods, are two tumor-agnostic predictive biomarkers for immunotherapy eligibility. However, there remains no consensus on the preferred testing method, nor on the type and extent of molecular testing required for optimal patient selection. This study investigates the correlation between MMR protein loss detected by IHC and MSI status identified through next-generation sequencing (NGS) to evaluate the concordance and potential complementary roles of these methods. MATERIAL AND

methodsA total of 139 tumor samples were analyzed for MSI using NGS. The cohort included colorectal carcinoma (n=51), pancreatic ductal adenocarcinoma (n=22), cholangiocarcinoma (n=9), non-small cell lung carcinoma (n=6), adenoid cystic carcinoma (n=6), gastric adenocarcinoma (n=6), high-grade serous ovarian carcinoma (n=5), and 34 other tumor types. IHC was performed to assess MLH1, MSH2, MSH6, and PMS2 protein expression. The correlation between MSI status and MMR protein loss was evaluated.

resultsTwelve tumors (8.6%) were classified as MSI-High (microsatellite instable). Among them, ten exhibited MMR protein loss, whereas two MSI-High tumors (a mucinous adenocarcinoma of omental origin and a mucinous colon adenocarcinoma) retained MMR protein expression. No MMR-deficient tumors were identified as MSI-Low (microsatellite stable/MSS).

conclusionA strong correlation exists between IHC-based MMR loss and NGS-based MSI detection. IHC remains widely used due to its accessibility and cost-effectiveness, whereas NGS offers higher accuracy and broader genomic insights. With its ability to detect multiple alterations simultaneously, NGS is particularly valuable when tissue is scarce. Combining both methods can improve diagnostic accuracy and guide optimal immunotherapy selection.

Indexed as

Biomarkers, TumorDNA Mismatch RepairHigh-Throughput Nucleotide SequencingImmunohistochemistryMicrosatellite InstabilityNeoplasmsAdultAgedFemaleHumansMaleMiddle AgedBiomarkers, Tumor

Identifiers

PMID40748292
PMCPMC12527557

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