Evidence map›Paper›PMID 27306525›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2016

Hypoxia can impair doxorubicin resistance of non-small cell lung cancer cells by inhibiting MRP1 and P-gp expression and boosting the chemosensitizing effects of MRP1 and P-gp blockers.

Yu-Lun Chen, Tsung-Ying Yang, Kun-Chieh Chen, Chieh-Liang Wu, Shih-Lan Hsu, Chi-Mei Hsueh

Abstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 45 citations in OpenAlex.

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  16. Methanol Extract of Aerial Parts ofMolecules (Basel, Switzerland) · 2019
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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

6 authors at 2 institutions in 1 country.

Yu-Lun ChenDepartment of Life Sciences, National Chung Hsing University, 145, Hsing-Da Rd, Taichung, 40227, Taiwan.
Tsung-Ying YangDepartment of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Kun-Chieh ChenDepartment of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Chieh-Liang WuDepartment of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Shih-Lan HsuDepartment of Education and Research, Taichung Veterans General Hospital, Taichung, Taiwan.
Chi-Mei HsuehDepartment of Life Sciences, National Chung Hsing University, 145, Hsing-Da Rd, Taichung, 40227, Taiwan. cmhsueh@dragon.nchu.edu.tw.
Taichung Veterans General Hospital · TWNational Chung Hsing University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-small cell lung cancers (NSCLCs) frequently exhibit resistance to therapeutic drugs, which seriously hampers their treatment. Here, we set out to assess the roles of the multidrug resistance protein 1 (MRP1) and P-glycoprotein (P-gp) in the doxorubicin (DOX) resistance of NSCLC cells, as well as the putative therapeutic efficacy of MRP1 and P-gp blockers on DOX-treated NSCLC cells.

methodsThe impact of DOX on cell survival, DOX efflux and MRP1 and P-gp expression was assessed in 5 different NSCLC-derived cell lines (parental CH27, A549, H1299, H460, and DOX resistant CH27) in the absence or presence of MK571 (MRP1 inhibitor) or Verapamil (P-gp inhibitor), under both normoxic and hypoxic conditions.

resultsWe found that in response to DOX treatment, NSCLC cells that express high levels of MRP1 and P-gp (such as CH27) showed a better DOX efflux and a higher DOX resistance. MK571 and Verapamil were found to abolish DOX resistance and to act as chemosensitizers for DOX therapy in all cell lines tested. We also found that hypoxia could inhibit MRP1 and P-gp expression in a HIF-1α-dependent manner, abolish DOX resistance and boost the chemosensitizer effect of MK571 and Verapamil on DOX treatment of all the NSCLC cells tested, except the DOX-resistant CH27 cells.

conclusionsFrom our data we conclude that MRP1 and P-gp play critical roles in the DOX resistance of the NSCLC cells tested. MRP1 and P-gp targeted therapy using MK571, Verapamil, CoCl

Indexed as

Antineoplastic AgentsATP-Binding Cassette, Sub-Family C ProteinsATP Binding Cassette Transporter, Subfamily B, Member 1Blotting, WesternCarcinoma, Non-Small-Cell LungCell HypoxiaCell Line, TumorDoxorubicinDrug Resistance, MultipleDrug Resistance, NeoplasmFlow CytometryHumansLung NeoplasmsPropionatesQuinolinesVerapamilAntineoplastic AgentsATP-Binding Cassette, Sub-Family C ProteinsATP Binding Cassette Transporter, Subfamily B, Member 1Doxorubicinmultidrug resistance-associated protein 1PropionatesQuinolinesVerapamilverlukastDoxorubicin resistanceHIF-1αHypoxiaMRP1NSCLCP-gp

Identifiers

PMID27306525
PMCPMC13001888
OpenAlexW2439464730

What OpenQuestion holds

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Registered trials

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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.