[磷脂酶Cβ1 (PLCB1)通过诱导上皮间质转移和抑制肿瘤免疫浸润促进胃腺癌转移,与患者预后不良相关]。

细胞与分子免疫学杂志 Pub Date : 2025-05-01
Lingping Yue, Junfeng Chen, Qianqian Gao
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引用次数: 0

摘要

目的探讨PLCB1表达是否导致胃腺癌转移及预后不良,并初步分析其机制。方法选择122例胃腺癌患者及其癌旁非癌组织,采用组织芯片技术免疫组化检测PLCB1、上皮钙粘蛋白(E-cadherin)、vimentin和CD8+ T细胞的表达水平,并由2名病理医师评分。根据PLCB1免疫组化评分将患者分为PLCB1高表达组(IHC≤90)和PLCB1低表达组(IHC≤90)。比较两组患者临床病理特征、上皮间充质转化(epithelial mesenchymal transition, EMT)相关蛋白及CD8+ T细胞表达差异。收集患者总生存期,采用COX回归分析和Kaplan-Meier曲线评价PLCB1表达水平与预后的关系。结果PLCB1在55例胃腺癌组织中高表达,而在邻近非癌组织中仅高表达12例。PLCB1高表达组肿瘤侵袭深度、淋巴结转移程度、TNM分期均高于PLCB1低表达组。卡方检验显示PLCB1表达水平与E-cadherin呈负相关(r=-0.339),与vimentin呈正相关(r=0.211),与CD8+ T细胞呈负相关(r=-0.343)。Kaplan-Meier曲线分析显示,PLCB1高表达的胃腺癌患者的总生存期和无病生存期明显降低。多因素COX回归分析显示,除淋巴结转移外,肿瘤浸润深度、TNM分期、E-cadherin、vimentin也是影响胃腺癌患者预后的独立因素。结论PLCB1在胃腺癌中高表达,与肿瘤侵袭性及预后密切相关。PLCB1可能诱导EMT,抑制CD8+ T细胞浸润,影响胃腺癌转移和免疫应答。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Phospholipase Cβ1 (PLCB1) promotes gastric adenocarcinoma metastasis by inducing epithelial mesenchymal transition and inhibiting tumour immune infiltration and is associated with poor patient prognosis].

Objective To investigate whether PLCB1 expression leads to gastric adenocarcinoma metastasis and poor prognosis, and to preliminarily analyze its mechanism. Methods 122 gastric adenocarcinoma patients and their adjacent non-cancerous tissues were selected, and tissue microarray technology was used to detect the expression levels of PLCB1, epithelial cadherin(E-cadherin), vimentin and CD8+ T cells by immunohistochemistry, and scored by two pathologists. According to the immunohistochemical score of PLCB1, the patients were divided into PLCB1 high expression group (IHC>90) and PLCB1 low expression group (IHC≤90). The clinical pathological characteristics, epithelial mesenchymal transition(EMT)-related proteins and CD8+ T cells expression differences between the two groups were compared. The overall survival of the patients was collected, and COX regression analysis and Kaplan-Meier curve were used to evaluate the relationship between PLCB1 expression level and prognosis. Results PLCB1 was highly expressed in 55 cases of gastric adenocarcinoma tissues, while only 12 cases in adjacent non-cancerous tissues. The tumor invasion depth, lymph node metastasis degree and TNM stage of the PLCB1 high expression group were higher than those of the PLCB1 low expression group. Chi-square test showed that PLCB1 expression level was negatively correlated with E-cadherin (r=-0.339), positively correlated with vimentin (r=0.211), and negatively correlated with CD8+ T cells (r=-0.343). Kaplan-Meier curve analysis showed that the overall survival and disease-free survival of gastric adenocarcinoma patients with high PLCB1 expression were significantly reduced. Multivariate COX regression analysis showed that except for lymph node metastasis, tumor invasion depth, TNM stage, E-cadherin and vimentin were also independent prognostic factors for gastric adenocarcinoma patients. Conclusion PLCB1 is highly expressed in gastric adenocarcinoma, and is closely related to tumor aggressiveness and prognosis. PLCB1 may induce EMT and inhibit CD8+ T cell infiltration to affect gastric adenocarcinoma metastasis and immune response.

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