Evidence map›Paper›PMID 34079223›Full record

ArticleDrug design, development and therapy2021

Enhanced Accumulation of Cisplatin in Ovarian Cancer Cells from Combination with Wedelolactone and Resulting Inhibition of Multiple Epigenetic Drivers.

Sadia Sarwar, Abir A Alamro, Amani A Alghamdi, Komal Naeem, Salamat Ullah, Muazzam Arif, Jun Qing Yu, Fazlul Huq

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

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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

8 authors at 4 institutions in 4 countries.

Sadia SarwarDiscipline of Biomedical Sciences, Sydney Medical School, The University of Sydney, Cumberland Campus, Sydney, NSW, Australia.ORCID 0000-0002-2514-8306
Abir A AlamroDepartment of Biochemistry, College of Science, King Saud University, Riyadh, 11495, Saudi Arabia.ORCID 0000-0002-6950-0092
Amani A AlghamdiDepartment of Biochemistry, College of Science, King Saud University, Riyadh, 11495, Saudi Arabia.ORCID 0000-0002-7251-1972
Komal NaeemDepartment of Pharmacology, Riphah Institute of Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Riphah International University, Islamabad, 44000, Pakistan.ORCID 0000-0001-8913-6825
Salamat UllahAcute Medicine, Northampton General Hospital, NHS, UK.ORCID 0000-0003-1822-3635
Muazzam ArifDepartment of Pharmaceutical Chemistry, Riphah Institute of Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.
Jun Qing YuDiscipline of Biomedical Sciences, Sydney Medical School, The University of Sydney, Cumberland Campus, Sydney, NSW, Australia.
Fazlul HuqEman Research Journal, Eman Research, Sydney, NSW, Australia.
King Saud University · SARiphah International University · PKThe University of Sydney · AUNorthampton General Hospital NHS Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCisplatin resistance is a major concern in ovarian cancer treatment. The aim of this study was to investigate if wedelolactone could perform better in resistant ovarian cancer cells when used in combination with cisplatin.

methodsGrowth inhibitory potential of wedelolactone and cisplatin was investigated through MTT reduction assay in ovarian cancer cell lines including A2780 (sensitive), A2780

resultsCisplatin and wedelolactone showed a dose-dependent growth inhibitory effect. RF value of wedelolactone was 1.1 in the case of A2780

conclusionThese findings have shown that additive outcome of drug combination in A2780

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCell Line, TumorCell ProliferationCisplatinCoumarinsDrug Resistance, NeoplasmDrug Screening Assays, AntitumorEpigenesis, GeneticFemaleHumansMolecular Docking SimulationOvarian NeoplasmsCisplatinCoumarinswedelolactoneA2780chemotherapy resistancecoumestangrowth inhibition

Identifiers

PMID34079223
PMCPMC8164677
OpenAlexW3164209971

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.