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p53和Rb的表达揭示了具有不同预后的胃神经内分泌癌亚型。

Expression of p53 and Rb reveal subtypes of gastric neuroendocrine carcinoma with distinct prognosis.

作者信息

Xing Jiazhang, Chen Jingci, You Tingting, Sun Zhao, Lu Tao, Cheng Yuejuan, Wu Huanwen, Bai Chunmei

机构信息

Department of Medical Oncology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.

Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.

出版信息

J Neuroendocrinol. 2023 Apr;35(4):e13257. doi: 10.1111/jne.13257. Epub 2023 Mar 25.

Abstract

Gastric neuroendocrine carcinoma (NEC) is a rare tumor with a poor prognosis. Due to its rarity and disparity in prevalence across populations, there is limited data on gastric NEC. TP53 and RB1 genetic alterations or expression were reported for predictive value in neuroendocrine neoplasm and classification in pulmonary large cell NEC. This study investigated the genetic alteration and protein expression of TP53 and RB1 in gastric NEC. Thirty-nine patients were categorized as type A and B subtypes by p53 and Rb expression. Patients with concurrent abnormal p53 and Rb expression were defined as the type A group, and the remainder were defined as the type B group. Significant differences in TNM stages, tumor size, and lymph node metastasis were observed between the two subtypes. Type A characteristic is an independent predictor for worse overall survival (HR: 3.27; 95% CI: 1.12-9.58; p = .022). We further evaluated and compared immunotherapy-related markers, including PD-L1 expression, CD8 T cell infiltration, tumor mutation burden, and microsatellite instability in these two subtypes, whereas no significant differences were detected.

摘要

胃神经内分泌癌(NEC)是一种罕见的肿瘤,预后较差。由于其罕见性以及不同人群中患病率的差异,关于胃NEC的数据有限。据报道,TP53和RB1基因改变或表达在神经内分泌肿瘤中具有预测价值,并且在肺大细胞NEC的分类中也有应用。本研究调查了胃NEC中TP53和RB1的基因改变及蛋白表达情况。39例患者根据p53和Rb表达分为A、B亚型。p53和Rb表达均异常的患者被定义为A组,其余患者被定义为B组。观察到这两种亚型在TNM分期、肿瘤大小和淋巴结转移方面存在显著差异。A亚型特征是总体生存较差的独立预测因素(HR:3.27;95%CI:1.12 - 9.58;p = 0.022)。我们进一步评估并比较了这两种亚型中与免疫治疗相关的标志物,包括PD-L1表达、CD8 T细胞浸润、肿瘤突变负荷和微卫星不稳定性,然而未检测到显著差异。

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