Abstract

c-Myc is an oncogene that is dysregulated in various cancers. Early gastric neoplasia with c-Myc expression has been reported as a more malignant lesion. This study clarifies the differences in c-Myc expression in early gastric neoplasia based on the WHO classification. Samples from 100 patients with differentiated-type early gastric neoplasia, who underwent endoscopic submucosal dissection between March 2020 and January 2021, were stained for c-Myc. One hundred lesions were classified as low-grade dysplasia, high-grade dysplasia, or intramucosal adenocarcinoma. The staining intensity and extent were scored. A hierarchical cluster analysis for a clinicopathological analysis among the groups, the chi-square test, Bonferroni correction, and residual analysis were performed. Subgroup one and two consisted of 39 patients; while subgroup three consisted of 22. Significant differences among various characteristics were observed between these subgroups. The frequency of low-grade dysplasia was significantly higher, while that of high-grade dysplasia was significantly lower in subgroup three. The frequency of intramucosal adenocarcinoma was significantly higher in subgroup one. The c-Myc positivity rate was significantly higher in subgroup one compared with that in subgroup three. c-Myc expression distinctly differed in early gastric neoplasia. c-Myc-negative low-grade dysplasia may be separately categorized from c-Myc-positive low-grade dysplasia, high-grade dysplasia, and intramucosal adenocarcinoma.

Highlights

  • We evaluated 107 patients who underwent endoscopic submucosal dissection at the Department of Gastroenterology, Takeda General Hospital, between March 2020 and January 2021, and were diagnosed with differentiated-type early gastric neoplasia based on histopathological examination

  • In terms of the invasion depth, the frequency of T1a was higher in low-grade dysplasia (LGD) (100%) and that of T1b was higher in intramucosal adenocarcinoma (IMA) (25%)

  • In terms of the gross morphology, the elevated type was more frequent in LGD (70.8%), the mixed type was more frequent in high-grade dysplasia (HGD) (11.1%), and the depressed type was more frequent in IMA (87.5%) (p < 0.01)

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Summary

Introduction

The use of a genetic analysis to clarify the molecular pathogenesis of gastric cancer has greatly increased in recent years [1]. In Japan, an intramucosal adenocarcinoma (IMA), and low-grade dysplasia (LGD) and high-grade dysplasia (HGD) are targeted for resection. A gain in c-Myc (8q24.21) is a genetic abnormality that occurs in the early stage of the disease and may be a driver gene [3]. The CNA analysis of 84 cases of gastric intramucosal epithelial tumors showed that the frequency of 8q gain was increased in HGD and IMA rather than in LGD [4]. The gain of a gene has been reported to correlate with an increased protein expression [5]

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