Evidence map›Paper›PMID 37614375›Full record

ArticleMolecular and clinical oncology2023

Prognostic value of translationally controlled tumor protein in colon cancer.

Dragomir Svetozarov Stoyanov, Nikolay Vladimirov Conev, Mariya Ivanova Penkova-Ivanova, Ivan Shterev Donev

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Article in Molecular and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Dragomir Svetozarov StoyanovDepartment of Oncology, Medical University Varna, Varna 9002, Bulgaria.
Nikolay Vladimirov ConevDepartment of Oncology, Medical University Varna, Varna 9002, Bulgaria.
Mariya Ivanova Penkova-IvanovaDepartment of Oncology, Medical University Varna, Varna 9002, Bulgaria.
Ivan Shterev DonevClinic of Medical Oncology, Nadezhda Hospital, Sofia 1330, Bulgaria.
Medical University of Varna · BG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The translationally controlled tumor protein (TCTP) is a highly conserved protein involved in a variety of normal cell functions and disease processes. Preclinical studies revealed that TCTP has anti-apoptotic properties, promotes cell growth and division and is involved in cancer progression by promoting invasion and metastasis. The present study explored the potential value of TCTP as a prognostic marker in colon cancer. A retrospective analysis of 74 patients with colon cancer was performed. Using immunohistochemistry, TCTP levels in the primary tumor were assessed semi-quantitatively by the calculation of cytoplasmic and nuclear H-score. Cytoplasmic TCTP levels in the primary tumor had no statistically significant association with disease-free survival (DFS), progression-free survival (PFS) and overall survival (OS) in the present patient population. Patients whose primary tumors had a negative nuclear TCTP expression had significantly improved clinical outcomes. The PFS for the negative nuclear TCTP expression group was 7.7 months [95% confidence interval (CI), 5.8-9.5] compared with 5.5 months (95% CI, 3.2-7.8) in the group with positive nuclear expression (P=0.023, Mantel-Cox log-rank). Patients with a negative nuclear expression of TCTP had a significantly higher median OS (22.2 months; 95% CI, 16.1-28.3) compared with those with positive TCTP nuclear expression (median 13.2 months; 95% CI, 10.1-16.3; P=0.008, Mantel-Cox log-rank). In a multivariate Cox regression model, a positive nuclear TCTP H-score was an independent risk factor for worse PFS and OS. The 1-year OS rate in the group with negative nuclear TCTP expression was 86.3% compared with 56.5% in patients with positive nuclear TCTP expression (P=0.008). The present study suggested that semiquantitative H-score measurement of TCTP levels in the nuclei of tumor cells from the primary tumor is a potential prognostic marker for clinical outcomes in patients with colon cancer.

Indexed as

colon cancerprognostic markersurvivaltranslationally controlled tumor protein

Identifiers

PMID37614375
PMCPMC10442730
OpenAlexW4385943976

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.