Evidence map›Paper›PMID 32370713›Full record

ArticleCurrent pharmaceutical biotechnology2020

Evaluation of Changes in the Expression Profile of mRNA and Proteinencoding Adiponectin in Ishikawa Cell Line under the Influence of Cisplatin - Preliminary Report.

Robert Kiełabsiński, Przemysław Kieszkowski, Beniamin O Grabarek, Dariusz Boroń

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Article in Current pharmaceutical biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
–field-weighted citation impact, top 95% 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

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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

2 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Robert KiełabsińskiDepartment of Obstetrics & Gynaecology ward, Health Center in Mikołów, Mikołów, Poland
Przemysław KieszkowskiVoivodeship Specialist Hospital in Wloclawek, Wloclawek, Poland
Beniamin O GrabarekDepartment of Histology, Cytophysiology and Embryology, Faculty of Medicine, University of Technology, Zabrze, Poland
Dariusz BorońDepartment of Histology, Cytophysiology and Embryology, Faculty of Medicine, University of Technology, Zabrze, Poland
Institute of Medical Technology and Equipment · PLCuiavian University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA reduced concentration of adiponectin is considered as an independent factor of the risk of inducing endometrial cancer. Cisplatin is a drug used in the therapy of this type of neoplasm. However, knowledge of the effects of cisplatin on the adiponectin level is still limited.

objectiveThe purpose of this study was to assess the impact of cisplatin depending on the concentration and time of exposition of the cells to the drug on the adiponectin level in the endometrial cancer cell line.

methodsCells of endometrial cancer cell line Ishikawa were exposed for 12,24 and 48 hour periods to cisplatin with the following concentrations: 2.5μM, 5μM, 10μM. The changes in the expression profile of adiponectin were compared to the RtqPCR reaction and ELISA test. The STATISTICA 13.0 PL program was used for statistical analysis (p<0.05).

resultsIn the culture without the drug, the concentration of adiponectin was statistically lower than in the cell culture incubated with the drug. Changes on the mRNA level seem to be more specific than on the protein level, although in both cases, the same trend in the expression changes was noted. DISCUSSION: The longer the time of exposition of the cells to the drug, the expression of mRNA, and the adiponectin protein increased. Changes in the expression profile were characterized statistically (p<0.05).

conclusionCisplatin, in a noticeable way, changes the expression profile of adiponectin. Molecular analysis indicated that in the case of endometrial cancer therapy should be implemented with a concentration of no less than 5 μM.

Indexed as

AdiponectinAntineoplastic AgentsCell Line, TumorCisplatinDose-Response Relationship, DrugEndometrial NeoplasmsFemaleGene ExpressionHumansRNA, MessengerAdiponectinAntineoplastic AgentsCisplatinRNA, MessengerAdiponectincisplatinendometrial cancerIshikawa cell linemolecular marker

Identifiers

PMID32370713
PMCPMC7604769
OpenAlexW3023460863

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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.