Unknown

Dataset Information

0

The Clinicopathological Features and Genetic Mutations in Gastric Cancer Patients According to EMAST and MSI Status.


ABSTRACT: Background: There has been no report regarding the clinicopathological features and genetic mutations regarding elevated microsatellite alterations at selected tetranucleotide repeats (EMAST) in gastric cancer (GC). Methods: The correlation among EMAST status, microsatellite instability (MSI) status, mutations of common GC-related genes and 16 DNA repair-associated genes, and the clinicopathological features were analyzed. Results: Among the 360 GC patients enrolled, there were 76 (21.1%) with EMAST+ tumors and 284 with EMAST- tumors, and 59 (16.4%) were MSI-high (MSI-H) tumors, and 301 were microsatellite stable (MSS) tumors. Patients with EMAST+ tumors exhibited an earlier pathological T category and had more genetic mutations in the PI3K/AKT pathway, ARID1A and DNA repair-associated genes than those with EMAST- tumors. Patients with MSI-H tumors have more genetic mutations in the PI3K/AKT pathway and DNA repair-associated genes than those with MSS tumors. In the subgroup analysis for MSI-H GC, EMAST+ tumors were associated with earlier pathological T and N categories, earlier TNM stages, higher frequency of DNA-repair-associated genetic mutations, and a better survival rate than EMAST- tumors. Conclusions: PI3K/AKT pathway mutations may play an important role in EMAST+ and/or MSI-H GC. EMAST+/MSI-H tumors seem to represent a different subtype of gastric cancer from EMAST-/MSI-H tumors.

SUBMITTER: Fang WL 

PROVIDER: S-EPMC7139949 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

The Clinicopathological Features and Genetic Mutations in Gastric Cancer Patients According to EMAST and MSI Status.

Fang Wen-Liang WL   Chen Ming-Huang MH   Huang Kuo-Hung KH   Chang Shih-Ching SC   Lin Chien-Hsing CH   Chao Yee Y   Lo Su-Shun SS   Li Anna Fen-Yau AF   Wu Chew-Wun CW   Shyr Yi-Ming YM  

Cancers 20200227 3


<i>Background:</i> There has been no report regarding the clinicopathological features and genetic mutations regarding elevated microsatellite alterations at selected tetranucleotide repeats (EMAST) in gastric cancer (GC). <i>Methods:</i> The correlation among EMAST status, microsatellite instability (MSI) status, mutations of common GC-related genes and 16 DNA repair-associated genes, and the clinicopathological features were analyzed. <i>Results:</i> Among the 360 GC patients enrolled, there w  ...[more]

Similar Datasets

| S-EPMC3285611 | biostudies-literature
| S-EPMC7352714 | biostudies-literature
| S-EPMC8606720 | biostudies-literature
| S-EPMC4129195 | biostudies-literature
| S-EPMC9031450 | biostudies-literature
2019-12-20 | GSE108166 | GEO
| S-EPMC3610773 | biostudies-literature
| S-EPMC6246951 | biostudies-literature
| S-EPMC6357506 | biostudies-literature
| S-EPMC5561143 | biostudies-literature