Evidence map›Paper›PMID 36293346›Full record

ArticleInternational journal of molecular sciences2022

Response of the Urothelial Carcinoma Cell Lines to Cisplatin.

Andrea Holíčková, Jan Roška, Eveline Órásová, Vladimíra Bruderová, Patrik Palacka, Dana Jurkovičová, Miroslav Chovanec

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Andrea HolíčkováBiomedical Research Center, Department of Genetics, Cancer Research Institute, Dúbravská cesta 9, 845 05 Bratislava, Slovakia.
Jan RoškaBiomedical Research Center, Department of Genetics, Cancer Research Institute, Dúbravská cesta 9, 845 05 Bratislava, Slovakia.
Eveline ÓrásováBiomedical Research Center, Department of Genetics, Cancer Research Institute, Dúbravská cesta 9, 845 05 Bratislava, Slovakia.
Vladimíra BruderováBiomedical Research Center, Department of Genetics, Cancer Research Institute, Dúbravská cesta 9, 845 05 Bratislava, Slovakia.
Patrik PalackaNational Cancer Institute, Klenová 1, 833 10 Bratislava, Slovakia.ORCID 0000-0003-4505-0952
Dana JurkovičováBiomedical Research Center, Department of Genetics, Cancer Research Institute, Dúbravská cesta 9, 845 05 Bratislava, Slovakia.
Miroslav ChovanecBiomedical Research Center, Department of Genetics, Cancer Research Institute, Dúbravská cesta 9, 845 05 Bratislava, Slovakia.ORCID 0000-0001-9120-5084
Cancer Research Institute of the Slovak Academy of Sciences · SKComenius University Bratislava · SK

Funding

Integrated Infrastructure Operational Program for the projects "Systemic public research infrastructure - biobank for cancer and rare diseases" ITMS: 313011AFG5Ministry of Education, Science Research and Sport of the Slovak Republic MVTS 34097104Ministry of Health of the Slovak Republic 2019/57-BMCSAV-1Slovak Research and Development Agency APVV-19-0286VEGA Grant Agency of the Slovak Republic 2/0053/19
6 · The paper itself

Abstract

Cisplatin (CDDP)-based chemotherapy is the standard of care in patients with muscle-invasive bladder cancer. However, in a large number of cases, the disease becomes resistant or does not respond to CDDP, and thus progresses and disseminates. In such cases, prognosis of patients is very poor. CDDP manifests its cytotoxic effects mainly through DNA damage induction. Hence, response to CDDP is mainly dependent on DNA damage repair and tolerance mechanisms. Herein, we have examined CDDP response in a panel of the urothelial carcinoma cell (UCC) lines. We characterized these cell lines with regard to viability after CDDP treatment, as well as kinetics of induction and repair of CDDP-induced DNA damage. We demonstrate that repair of CDDP-induced DNA lesions correlates, at least to some extent, with CDDP sensitivity. Furthermore, we monitored expression of the key genes involved in selected DNA repair and tolerance mechanisms, nucleotide excision repair, homologous recombination and translesion DNA synthesis, and show that it differs in the UCC lines and positively correlates with CDDP resistance. Our data indicate that CDDP response in the UCC lines is dependent on DNA damage repair and tolerance factors, which may, therefore, represent valuable therapeutic targets in this malignancy.

Indexed as

Antineoplastic AgentsCarcinoma, Transitional CellUrinary Bladder NeoplasmsCell LineCisplatinDNADNA RepairHumansAntineoplastic AgentsCisplatinDNAbladder cancercisplatinDNA damage repair and tolerancehomologous recombinationnucleotide excision repairtranslesion DNA synthesis

Identifiers

PMID36293346
PMCPMC9604399
OpenAlexW4306765597

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.