Evidence map›Paper›PMID 30251669›Full record

ArticleBiochimica et biophysica acta. General subjects2018

Nitric oxide reverses drug resistance by inhibiting ATPase activity of p-glycoprotein in human multi-drug resistant cancer cells.

Birandra K Sinha, Carl D Bortner, Ronald P Mason, Ronald E Cannon

Abstract read
In one paragraph

Article in Biochimica et biophysica acta. General subjects, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 37 citations in OpenAlex.

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  4. Mechanisms of Cell Death Induced by Erastin in Human Ovarian Tumor Cells.International journal of molecular sciences · 2024
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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

4 authors at 1 institution in 1 country.

Birandra K SinhaImmunity, Inflammation and Disease Laboratory, USA. Electronic address: sinha1@niehs.nih.gov.
Carl D BortnerLaboratory of Signal Transduction, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC, USA.
Ronald P MasonImmunity, Inflammation and Disease Laboratory, USA.
Ronald E CannonLaboratory of Signal Transduction, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC, USA.
National Institute of Environmental Health Sciences · US

Funding

Intramural NIH HHS Z99 ES999999
6 · The paper itself

Abstract

backgroundDevelopment of resistance to chemotherapy drugs is a significant problem in treating human malignancies in the clinic. Overexpression of drug efflux proteins, including P-170 glycoprotein (P-gp), an ATP-dependent efflux protein, is one of the main mechanisms responsible for multi-drug resistance (MDR). Because our previous studies have shown that nitric oxide (

resultsCytotoxicity and cellular accumulation studies showed that

conclusionsThe reversal of drug resistance is due to inhibition of the ATPase activity by GENERAL SIGNIFICANCE: Appropriately designed NO donors would be ideal for the treatment of P-gp-overexpressing tumors in the clinic.

Indexed as

Drug Resistance, MultipleDrug Resistance, NeoplasmAdenosine TriphosphatasesAntibiotics, AntineoplasticATP Binding Cassette Transporter, Subfamily BATP Binding Cassette Transporter, Subfamily B, Member 1Blotting, WesternCell DeathCell Line, TumorDNA DamageDoxorubicinHumansMicroscopy, ConfocalNitric OxidePaclitaxelABCB1 protein, humanAdenosine TriphosphatasesAntibiotics, AntineoplasticATP Binding Cassette Transporter, Subfamily BATP Binding Cassette Transporter, Subfamily B, Member 1DoxorubicinNitric OxidePaclitaxelAdriamycinFree radicalMulti-drug resistanceNitric OxideP-gp proteinTaxol

Identifiers

PMID30251669
PMCPMC6195836
OpenAlexW2889042148

What OpenQuestion holds

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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.