TPBG作为胃癌新的预测指标的深入研究。

IF 5.3
Lianlei Yang, Chunyan Weng, Yaping Zhang, Yu Zhao, Kexin Chen, Guodong Li, Xueqing Zhong, Chenghai He
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引用次数: 0

摘要

滋养细胞糖蛋白(TPBG)在特定癌症的生长中起着重要作用,但其与胃癌(GC)的关系尚不清楚。本研究旨在分析胃癌中TPBG水平的波动,并评估TPBG表达与胃癌患者预后的关系。在Cancer Genome Atlas (TCGA)和Genotype-Tissue expression (GTEx)数据库中检测胃癌组织和正常胃组织中TPBG的表达,并进一步从HPA数据库中提取免疫组化图像,进行Western blot验证。采用Kaplan-Meier和COX回归分析探讨TPBG与胃癌患者生存率的关系。利用GO和KEGG数据富集与TPBG相关的基因。采用体外和体内肿瘤模型评价TPBG在胃癌中的作用。Western blot检测TPBG敲除后PI3K/AKT信号通路蛋白的表达。采用CIBERSOFT和ssGSEA方法分析免疫浸润。通过使用GSVA评估TPBG与浸润肿瘤的免疫细胞之间的关系。TPBG在一些肿瘤组织(包括胃癌)中的表达高于邻近的非癌组织。TPBG水平升高预示着较差的预后,如GC患者的总生存期、病理分期和治疗反应较差。富集分析主要集中于生物过程,如外部包封结构的组织、细胞外结构和胶原蛋白代谢。生物学实验进一步证明,TPBG敲低成功地抑制了GC细胞的进展、迁移和侵袭。Western blot分析显示,TPBG敲低抑制PI3K/AKT信号通路。此外,TPBG与GC中免疫细胞的浸润有关,而免疫细胞的浸润与巨噬细胞的表达相关。TPBG与胃癌组织和细胞的恶性行为呈正相关,提示TPBG可用于胃癌的诊断和预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In-Depth Examination of TPBG as a New Predictive Indicator for Gastric Cancer

In-Depth Examination of TPBG as a New Predictive Indicator for Gastric Cancer

Trophoblast glycoprotein (TPBG) plays a significant part in the growth of specific cancers, yet its connection to gastric cancer (GC) remains uncertain. This research seeks to analyse the fluctuation in TPBG levels in GC and evaluate how TPBG expression relates to the prognosis of GC patients. TPBG expression in GC and normal gastric tissues was investigated in The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) database, further extracting the immunohistochemistry images from HPA database and validating by Western blot. The connection between TPBG and GC patients' survival rates was investigated by Kaplan–Meier and COX regression analysis. Genes related to TPBG were enriched using GO and KEGG data. In vitro and in vivo tumour models were utilised to evaluate the function of TPBG in GC. Western blot analysis was performed to detect the expression of PI3K/AKT signalling pathway proteins following TPBG knockdown. Immune infiltration was analysed using the CIBERSOFT and ssGSEA methods. The association between TPBG and immune cells that infiltrate tumours was evaluated through the utilisation of GSVA. TPBG expression increased in several tumour tissues (including GC) more than in adjacent noncancerous tissues. Elevated TPBG level predicted worse outcomes, such as poorer overall survival, pathological stage, and therapy response in GC. Enrichment analysis primarily focused on biological processes like the organisation of external encapsulating structures, extracellular structure, and collagen metabolism. Biological experiments further demonstrated that TPBG knockdown successfully inhibits the progression, migration, and invasion of GC cells. Western blot analysis revealed that TPBG knockdown inhibits the PI3K/AKT signalling pathway. Furthermore, TPBG is associated with the infiltration of immune cells in GC, which correlates with the expression of macrophage cells. There is a positive relationship between TPBG and malignant behaviour of GC tissues and cells, suggesting that TPBG can be useful for diagnosing and prognosing GC.

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来源期刊
CiteScore
11.50
自引率
0.00%
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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