Tang Chao-Tao, Chen Si-Hai
Department of Gastroenterology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Front Med (Lausanne). 2021 Dec 23;8:758977. doi: 10.3389/fmed.2021.758977. eCollection 2021.
The incidence of early-onset gastric cancer (GC) that was diagnosed at <50 years is increasing, but there is a knowledge gap on early-onset early-stage GC (EEGC) that was defined as early-onset GC limited to the mucosa or submucosa. Therefore, we comprehensively analysed the clinical features based on Lauren type. Logistic and Cox analyses were used to investigate risk factors for lymph node metastasis (LNM) and prognosis, respectively. Propensity score matching (PSM) was used to adjust confounding factors. Protein mass spectrometry analysis was used to explore the molecular mechanism of LNM. Our study included 581 patients with EEGC from the Surveillance, Epidemiology, and End Results (SEER) database and 226 patients with EEGC from our own centre. We identified intestinal type, T1b stage, and tumour size (>3 cm) as risk factors for LNM using SEER and our own data. We also found that the prognosis of patients with intestinal-type EEGC was poorer than patients with diffuse-type EEGC, and T1b stage and positive LNM were hazard factors for survival. After analysing the expression of proteins between positive and negative LNM in the intestinal or diffuse type, we found no similar proteins between these groups. The differentially expressed genes (DEGs) in the intestinal type functioned as epithelial cell signalling in . The DEGs in the diffuse type functioned in the tricarboxylic acid cycle (TCA cycle) and oxidative phosphorylation. For EEGC, our study was the first report to demonstrate that the intestinal type was a risk factor for LNM and survival compared to the diffuse type, and the oncogenic expression promoting the occurrence of LNM was different. These findings suggest that clinicians should pay more attention to intestinal-type EEGC than diffuse-type EEGC.
50岁以前确诊的早发性胃癌(GC)发病率正在上升,但对于定义为局限于黏膜或黏膜下层的早发性早期胃癌(EEGC),目前存在认知空白。因此,我们基于Lauren分型全面分析了其临床特征。分别采用逻辑回归和Cox分析来研究淋巴结转移(LNM)的危险因素和预后情况。使用倾向评分匹配(PSM)来调整混杂因素。采用蛋白质质谱分析来探索LNM的分子机制。我们的研究纳入了来自监测、流行病学和最终结果(SEER)数据库的581例EEGC患者以及来自我们自己中心的226例EEGC患者。利用SEER数据和我们自己的数据,我们确定肠型、T1b期和肿瘤大小(>3cm)为LNM的危险因素。我们还发现,肠型EEGC患者的预后比弥漫型EEGC患者差,且T1b期和LNM阳性是生存的危险因素。在分析肠型或弥漫型中LNM阳性和阴性之间蛋白质的表达后,我们发现这些组之间没有相似的蛋白质。肠型中的差异表达基因(DEGs)在……中发挥上皮细胞信号传导功能。弥漫型中的DEGs在三羧酸循环(TCA循环)和氧化磷酸化中发挥作用。对于EEGC,我们的研究首次表明,与弥漫型相比,肠型是LNM和生存的危险因素,且促进LNM发生的致癌表达不同。这些发现表明,临床医生应比弥漫型EEGC更关注肠型EEGC。