본문으로 건너뛰기
← 뒤로

Machine Learning-Based Pathomics Signature in Predicting MSH2 Expression and Prognosis in Gastric Cancer.

Clinical and translational gastroenterology 2026 Vol.17(4) p. e00985

Zhang ZR, Wang Y, Yan WW, Li HR, Cheng ZW, Han T, Zhang C, Wang XM

📝 환자 설명용 한 줄

[INTRODUCTION] Gastric cancer (GC) is one of the most prevalent and lethal gastrointestinal malignancies.

이 논문을 인용하기

BibTeX ↓ RIS ↓
APA Zhang ZR, Wang Y, et al. (2026). Machine Learning-Based Pathomics Signature in Predicting MSH2 Expression and Prognosis in Gastric Cancer.. Clinical and translational gastroenterology, 17(4), e00985. https://doi.org/10.14309/ctg.0000000000000985
MLA Zhang ZR, et al.. "Machine Learning-Based Pathomics Signature in Predicting MSH2 Expression and Prognosis in Gastric Cancer.." Clinical and translational gastroenterology, vol. 17, no. 4, 2026, pp. e00985.
PMID 41649179

Abstract

[INTRODUCTION] Gastric cancer (GC) is one of the most prevalent and lethal gastrointestinal malignancies. MutS homolog 2 (MSH2), a DNA mismatch repair protein, has emerged as a promising prognostic biomarker. However, traditional histopathological evaluation is limited by restricted fields compared with whole-slide imaging. This study aimed to investigate whether machine learning-derived digital pathomics features could predict MSH2 expression and clinical outcomes in GC.

[METHODS] Hematoxylin and eosin-stained whole-slide images from 234 patients were analyzed to extract quantitative pathological features. A pathomics score (PS) was developed to estimate MSH2 expression. The association between PS and overall survival (OS) was assessed using univariate and multivariate Cox regression. Survival differences between high-PS and low-PS groups were evaluated using Kaplan-Meier analysis. Functional enrichment and immune infiltration analyses were performed to explore potential biological mechanisms.

[RESULTS] Digital image analysis identified pathomics features associated with MSH2 expression. The PS served as a surrogate marker for MSH2 and effectively stratified patients into prognostic subgroups with significant different OS. High PS was associated with features suggestive of a stronger antitumor immune response, whereas low PS was linked to an immunosuppressive microenvironment.

[DISCUSSION] The machine learning-derived pathomics signature shows potential in predicting MSH2 expression. It can serve as a complementary research tool and provide clinically meaningful prognostic information for GC.

MeSH Terms

Humans; Stomach Neoplasms; MutS Homolog 2 Protein; Machine Learning; Male; Female; Prognosis; Middle Aged; Biomarkers, Tumor; Aged; Tumor Microenvironment; Kaplan-Meier Estimate; Stomach