Evidence map›Paper›PMID 20812902›Full record

ReviewCurrent drug metabolism2010

Structure and function of the human breast cancer resistance protein (BCRP/ABCG2).

Zhanglin Ni, Zsolt Bikadi, Mark F Rosenberg, Qingcheng Mao

Open access · bronzeAbstract readReview
In one paragraph

Review in Current drug metabolism, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

107 citing papers in PubMed, 267 citations in OpenAlex.

  1. Review
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  12. Molecular Characteristics and Polymorphisms of Buffalo (Animals : an open access journal from MDPI · 2023
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  20. Characterization of a Potent, Selective, and Safe Inhibitor, Ac15(Az8)International journal of molecular sciences · 2022
    Article

47 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

Zhanglin NiDepartment of Pharmaceutics, School of Pharmacy, University of Washington, Health Science Building H272, 1959 NE Pacific Street, Seattle, Washington 98195-7610, USA.
Zsolt Bikadi
Mark F Rosenberg
Qingcheng Mao
University of Washington · USUniversity of Manchester · GB

Funding

Mechanism of Drug Transport by BCRP/ABCG2R01GM073715 · NIGMS · UNIVERSITY OF WASHINGTON · PI MAO, QINGCHENG · 2006 to 2010
$1.3M
NIGMS NIH HHS GM073715NIGMS NIH HHS R01 GM073715Wellcome TrustWellcome Trust 081406/Z/06/Z
6 · The paper itself

Abstract

The human breast cancer resistance protein (BCRP/ABCG2) is the second member of the G subfamily of the large ATP-binding cassette (ABC) transporter superfamily. BCRP was initially discovered in multidrug resistant breast cancer cell lines where it confers resistance to chemotherapeutic agents such as mitoxantrone, topotecan and methotrexate by extruding these compounds out of the cell. BCRP is capable of transporting non-chemotherapy drugs and xenobiotiocs as well, including nitrofurantoin, prazosin, glyburide, and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine. BCRP is frequently detected at high levels in stem cells, likely providing xenobiotic protection. BCRP is also highly expressed in normal human tissues including the small intestine, liver, brain endothelium, and placenta. Therefore, BCRP has been increasingly recognized for its important role in the absorption, elimination, and tissue distribution of drugs and xenobiotics. At present, little is known about the transport mechanism of BCRP, particularly how it recognizes and transports a large number of structurally and chemically unrelated drugs and xenobiotics. Here, we review current knowledge of structure and function of this medically important ABC efflux drug transporter.

Indexed as

Antineoplastic AgentsATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 2Drug Resistance, MultipleDrug Resistance, NeoplasmHumansModels, MolecularMolecular StructureMutant ProteinsNeoplasm ProteinsStructural Homology, ProteinSubstrate SpecificityXenobioticsABCG2 protein, humanAntineoplastic AgentsATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 2Mutant ProteinsNeoplasm ProteinsXenobiotics

Identifiers

PMID20812902
PMCPMC2950214
OpenAlexW2137683119

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.