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胃癌患者 TRIM44 表达的临床意义。

Clinical Significance of TRIM44 Expression in Patients with Gastric Cancer.

机构信息

Department of Gastroenterology and Hepatology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Department of Biochemistry, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran.

出版信息

Asian Pac J Cancer Prev. 2022 May 1;23(5):1725-1731. doi: 10.31557/APJCP.2022.23.5.1725.

DOI:10.31557/APJCP.2022.23.5.1725
PMID:35633558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9587887/
Abstract

BACKGROUND

Despite the tremendous efforts in finding a valuable markers for risk stratifying gastric cancer (GC) patients; still, management of this cancer faces multiple obstacles. Given this, we designed a study to explore the possible relationship between the tripartite motif-containing 44 (TRIM44) gene expression, and the outcome of the GC patients.

METHODS

The real-time quantitative PCR method was used to evaluate the mRNA expression level of TRIM44, and β-catenin in fresh primary tumor and adjacent normal tissues collected from 40 GC patients. The Pearson's correlation test, Kaplan-Meier method, and Cox proportional-hazards regression were performed to examine the association of TRIM44 expression with some clinicopathological data and the patients' overall survival (OS).

RESULTS

The expression level of both TRIM44 and β-catenin was remarkably higher in GC tissues than in normal tissues (Fold change=1.71, p=0.004). In subgroup analysis based on the TRIM44 expression, pateints with high TRIM44 expression level exhibited poorer overall survival (HR = 1.46, 95% CI: 1.07-1.98, p=0.016). More strikingly, a positive correlation was also found between the expression of TRIM44 and β-catenin in GC, indicating that TRIM44 might exert its oncogenic activities probably through the β-catenin axis.

CONCLUSION

This study highlighted the potent value of TRIM44 as an independent prognostic factor in gastric cancer and shed light on the probable interplay between this tripartite motif-containing protein and β-catenin. However, further investigations, especially with a larger sample size, are required to study the effect of TRIM44 in GC more precisely.

摘要

背景

尽管在寻找有价值的胃癌(GC)患者风险分层标志物方面付出了巨大努力,但这种癌症的治疗仍然面临诸多障碍。有鉴于此,我们设计了一项研究,旨在探索三肽基含 44 (TRIM44)基因表达与 GC 患者预后之间的可能关系。

方法

采用实时定量 PCR 方法检测 40 例 GC 患者新鲜原发肿瘤及相邻正常组织中 TRIM44 和 β-catenin 的 mRNA 表达水平。采用 Pearson 相关检验、Kaplan-Meier 法和 Cox 比例风险回归分析 TRIM44 表达与部分临床病理数据及患者总生存期(OS)的关系。

结果

GC 组织中 TRIM44 和 β-catenin 的表达水平均明显高于正常组织(Fold change=1.71,p=0.004)。基于 TRIM44 表达的亚组分析显示,高 TRIM44 表达水平的患者总生存期较差(HR=1.46,95%CI:1.07-1.98,p=0.016)。更引人注目的是,GC 中 TRIM44 表达与 β-catenin 之间存在正相关,表明 TRIM44 可能通过 β-catenin 轴发挥其致癌活性。

结论

本研究强调了 TRIM44 作为独立预后因素在胃癌中的潜在价值,并揭示了这种三肽基含蛋白与 β-catenin 之间可能的相互作用。然而,需要进一步的研究,特别是更大的样本量,以更精确地研究 TRIM44 在 GC 中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0140/9587887/0761d058d291/APJCP-23-1725-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0140/9587887/66acfc4f3056/APJCP-23-1725-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0140/9587887/3f360e7807a8/APJCP-23-1725-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0140/9587887/0761d058d291/APJCP-23-1725-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0140/9587887/66acfc4f3056/APJCP-23-1725-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0140/9587887/3f360e7807a8/APJCP-23-1725-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0140/9587887/0761d058d291/APJCP-23-1725-g003.jpg

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本文引用的文献

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The PI3K/Akt/mTOR signaling pathway in gastric cancer; from oncogenic variations to the possibilities for pharmacologic interventions.胃癌中的 PI3K/Akt/mTOR 信号通路:从致癌变异到药物干预的可能性。
Eur J Pharmacol. 2021 May 5;898:173983. doi: 10.1016/j.ejphar.2021.173983. Epub 2021 Feb 26.
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Decreased expression of TRIM3 gene predicts a poor prognosis in gastric cancer.
TRIM蛋白在胃癌中的作用及机制
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TRIM3 基因表达降低预示胃癌预后不良。
J Gastrointest Cancer. 2022 Mar;53(1):179-186. doi: 10.1007/s12029-020-00563-0. Epub 2021 Jan 7.
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The PI3K-AKT-mTOR Pathway and Prostate Cancer: At the Crossroads of AR, MAPK, and WNT Signaling.PI3K-AKT-mTOR 通路与前列腺癌:AR、MAPK 和 WNT 信号的十字路口。
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Family History of Gastric Cancer and Treatment.胃癌家族史和治疗。
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Knockdown of TRIM47 inhibits breast cancer tumorigenesis and progression through the inactivation of PI3K/Akt pathway.敲低 TRIM47 通过抑制 PI3K/Akt 通路抑制乳腺癌的发生发展。
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