Arakawa Noriyuki, Irisawa Atsushi, Ishida Kazuyuki, Tsunoda Takuya, Yamaguchi Yoshiko, Shibukawa Goro, Eizuka Makoto, Tokioka Shunzo, Wakabayashi Hiroto
Department of Gastroenterology, Takeda General Hospital, Aizuwakamatsu 965-8585, Japan.
Department of Gastroenterology, Dokkyo Medical University School of Medicine, Mibu 321-0293, Japan.
J Clin Med. 2022 Jan 21;11(3):544. doi: 10.3390/jcm11030544.
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.
c-Myc是一种在多种癌症中失调的癌基因。据报道,具有c-Myc表达的早期胃肿瘤是一种更具恶性的病变。本研究基于世界卫生组织(WHO)分类法阐明了早期胃肿瘤中c-Myc表达的差异。对2020年3月至2021年1月间接受内镜黏膜下剥离术的100例分化型早期胃肿瘤患者的样本进行c-Myc染色。100个病变被分类为低级别异型增生、高级别异型增生或黏膜内腺癌。对染色强度和范围进行评分。对各组间进行临床病理分析的层次聚类分析、卡方检验、Bonferroni校正和残差分析。第一组和第二组由39例患者组成;而第三组由22例患者组成。这些亚组之间在各种特征上观察到显著差异。第三组中低级别异型增生的频率显著更高,而高级别异型增生的频率显著更低。第一组中黏膜内腺癌的频率显著更高。与第三组相比,第一组中c-Myc阳性率显著更高。早期胃肿瘤中c-Myc表达明显不同。c-Myc阴性的低级别异型增生可能与c-Myc阳性的低级别异型增生、高级别异型增生和黏膜内腺癌分开分类。