Evidence map›Paper›PMID 35845310›Full record

ArticleGastroenterology and hepatology from bed to bench2022

Clinical significance of TRIM29 expression in patients with gastric cancer.

Javad Farhadi, Jamshid Mehrzad, Hassan Mehrad-Majd, Alireza Motavalizadehkakhky

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Article in Gastroenterology and hepatology from bed to bench, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 citing papers in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Javad FarhadiDepartment of Biochemistry, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran.
Jamshid MehrzadDepartment of Biochemistry, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran.
Hassan Mehrad-MajdCancer Molecular Pathology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Alireza MotavalizadehkakhkyDepartment of Chemistry, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: The present study aimed to evaluate the expression profile, prognostic value, and possible correlation of TRIM29 with β-catenin, Cyclin D, and Bcl2 in Iranian patients with GC. Background: Tripartite Motif Containing 29 (TRIM29) has been reported to function as an oncogene or a tumor suppressor depending on the tumor type. This contextual function has created a controversial situation that needs to be fully delineated in various cancers. Although few studies have reported an elevated TRIM29 expression in gastric cancer (GC), its clinicopathological and prognostic values as well as possible molecular mechanisms are yet to be re-evaluated in different populations. Methods: Real-time quantitative PCR was used to detect TRIM29, β-catenin, Cyclin D, and Bcl-2 expression in 40 GC and their adjacent normal tissues. Patients were further stratified into high and low expression subgroups based on their TRIM29 expression levels. The association of TRIM29 expression level with β-catenin, Cyclin D, BCL2, some clinicopathological features, and patients' overall survival (OS) was assessed using appropriate statistical analyses. Results: The results showed a significantly higher TRIM29 expression level in GC tissues compared with their corresponding normal tissues (fold change=2.94, Conclusion: Overexpression of TRIM29 is associated with poor prognosis in patients with GC and is probably mediated through β-catenin/Cyclin D/Bcl2 pathway and can be considered as a potential independent prognostic marker.

Indexed as

Bcl-2Cyclin DGastric CancerPrognosisSurvivalTRIM29Β-Catenin

Identifiers

PMID35845310
PMCPMC9275739

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