Evidence map›Paper›PMID 39237917›Full record

ArticleBMC cancer2024

Prognostic value of nucleotide excision repair and translesion DNA synthesis proteins in muscle-infiltrating bladder carcinoma.

Patrik Palacka, Andrea Holíčková, Jan Roška, Peter Makovický, Miroslava Vallová, Csaba Biró, Eveline Órásová, Jana Obertová, Jozef Mardiak, Thomas A Ward and 2 more

Abstract read
In one paragraph

Article in BMC cancer, 2024. 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

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Patrik Palacka *2nd Department of Oncology, Comenius University, Faculty of Medicine and National Cancer Institute, Bratislava, Slovakia. pal_patrick@yahoo.co.uk.
Andrea Holíčková *Cancer Research Institute, Biomedical Research Center of the Slovak Academy of Sciences, Bratislava, Slovakia.
Jan RoškaCancer Research Institute, Biomedical Research Center of the Slovak Academy of Sciences, Bratislava, Slovakia.
Peter MakovickýCancer Research Institute, Biomedical Research Center of the Slovak Academy of Sciences, Bratislava, Slovakia.
Miroslava VallováDepartment of Pathology, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
Csaba BiróDepartment of Pathology, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
Eveline ÓrásováCancer Research Institute, Biomedical Research Center of the Slovak Academy of Sciences, Bratislava, Slovakia.
Jana Obertová2nd Department of Oncology, Comenius University, Faculty of Medicine and National Cancer Institute, Bratislava, Slovakia.
Jozef Mardiak2nd Department of Oncology, Comenius University, Faculty of Medicine and National Cancer Institute, Bratislava, Slovakia.
Thomas A WardXCellR8 Ltd, Sci-Tech Daresbury, Cheshire, WA4 4AB, UK.
Karol KajoDepartment of Pathology, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
Miroslav ChovanecCancer Research Institute, Biomedical Research Center of the Slovak Academy of Sciences, Bratislava, Slovakia. miroslav.chovanec@savba.sk.

Funding

Integrated infrastructure operational program for the projects 'Systemic public research infrastructure - Biobank for cancer and rare diseases' co-financed by the European Regional Development Fund 313011AFG5VEGA Agency of the Slovak Republic 2/0075/23
6 · The paper itself

Abstract

backgroundCisplatin (CDDP) remains a key agent in the treatment of muscle-infiltrating bladder carcinoma (MIBC). However, a proportion of MIBC patients do not respond to chemotherapy, which may be caused by the increased repair of CDDP-induced DNA damage. The purpose of this study was to explore the prognostic value of proteins involved in nucleotide excision repair (NER) and translesion DNA synthesis (TLS) in MIBC patients.

methodsThis is a retrospective analysis of 86 MIBC patients. The XPA, XPF, XPG, ERCC1, POLI, POLH and REV3L proteins were stained in primary bladder tumors and their levels were analyzed both in the total cohort and in a subgroup with metastatic urothelial carcinoma (mUC) that received gemcitabine and CDDP as a first-line therapy. Both cohorts were divided by percentage of cancer cells stained positive for each protein into subgroups with high and low expression. In the same manner, the combined expression of NER (XPA + ERCC1 + XPF + XPG) and TLS (POLI + POLH + REV3L), as the whole pathways, was analyzed.

resultsMortality was 89.5% at the median follow-up of 120.2 months. In the total cohort, patients with tumors stained positive for XPA, XPG and POLI had significantly worse overall survival (OS) compared to those with negative staining [hazard ratio (HR) = 0.60, 0.62 and 0.53, respectively]. Both XPG and POLI were independent prognostic factors in multivariate analyses (MVA). In addition, an increase in NER and TLS pathway expression was significantly associated with worse OS in the total cohort (HR = 0.54 and 0.60, respectively). In the mUC subgroup, high POLI expression was associated with significant deterioration of OS (HR = 0.56) in univariate analyses, and its independent prognostic value was shown in MVA.

conclusionsOur study showed significant correlations between the tumor expression of XPG and POLI, as well as NER and TLS as the whole pathways, and inferior OS. Hence, they could constitute prognostic biomarkers and potentially promising therapeutic targets in MIBC. However, a prospective trial is required for further validation, thereby overcoming the limitations of this study.

Indexed as

DNA RepairUrinary Bladder NeoplasmsAdultAgedAged, 80 and overBiomarkers, TumorCisplatinDeoxycytidineDNA-Binding ProteinsEndonucleasesExcision RepairFemaleHumansMaleMiddle AgedPrognosisBiomarkers, TumorCisplatinDeoxycytidineDNA-Binding ProteinsEndonucleasesBladder carcinomaCisplatinDNA damageGemcitabineMuscle-infiltrating bladder carcinomaNucleotide excision repairTranslesion DNA synthesis

Identifiers

PMID39237917
PMCPMC11376035

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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.