Evidence map›Paper›PMID 34717915›Full record

ArticleChemico-biological interactions2022

A new porphyrin as selective substrate-based inhibitor of breast cancer resistance protein (BCRP/ABCG2).

Ingrid Fatima Zattoni, Thales Kronenberger, Diogo Henrique Kita, Lais Danciguer Guanaes, Matheus Murmel Guimarães, Larissa de Oliveira Prado, Melanie Ziasch, Luis C Vesga, Fabiane Gomes de Moraes Rego, Geraldo Picheth and 9 more

Open access · greenAbstract read
In one paragraph

Article in Chemico-biological interactions, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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  9. The frequency of rs2231142 inPharmacogenomics · 2023
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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

19 authors at 5 institutions in 4 countries.

Ingrid Fatima ZattoniPharmaceutical Sciences Graduate Program, Laboratory of Cancer Drug Resistance, Federal University of Parana, Curitiba, PR, Brazil.
Thales KronenbergerSchool of Pharmacy, University of Eastern Finland, Faculty of Health Sciences, Kuopio, 70211, Finland; Department of Medical Oncology and Pneumology, Internal Medicine VIII, University Hospital of Tübingen, Otfried-Müller-Strasse 14, 72076, Tübingen, Germany.
Diogo Henrique KitaPharmaceutical Sciences Graduate Program, Laboratory of Cancer Drug Resistance, Federal University of Parana, Curitiba, PR, Brazil; Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Lais Danciguer GuanaesDepartment of Pharmacy, Federal University of Parana, Curitiba, PR, Brazil.
Matheus Murmel GuimarãesDepartment of Pharmacy, Federal University of Parana, Curitiba, PR, Brazil.
Larissa de Oliveira PradoDepartment of Clinical Analysis, Federal University of Parana, Curitiba, PR, Brazil.
Melanie ZiaschDepartment of Clinical Analysis, Federal University of Parana, Curitiba, PR, Brazil.
Luis C VesgaSchool of Pharmacy, University of Eastern Finland, Faculty of Health Sciences, Kuopio, 70211, Finland; Research Group in Biochemistry and Microbiology (GIBIM), School of Chemistry, Industrial University of Santander, A.A. 678, Bucaramanga, Colombia; Research Group on Organic Compounds of Medicinal Interest (CODEIM), Technological Park of Guatiguara, Industrial University of Santander, A. A. 678, Piedecuesta, Colombia.
Fabiane Gomes de Moraes RegoDepartment of Clinical Analysis, Federal University of Parana, Curitiba, PR, Brazil.
Geraldo PichethDepartment of Clinical Analysis, Federal University of Parana, Curitiba, PR, Brazil.
Marcos Brown GonçalvesDepartment of Physics, Federal Technological University of Paraná, 80230-901 Curitiba, Parana, Brazil.
Miguel D NosedaDepartment of Biochemistry and Molecular Biology, Federal University of Paraná, Curitiba, Paraná, Brazil.
Diogo R B DucattiDepartment of Biochemistry and Molecular Biology, Federal University of Paraná, Curitiba, Paraná, Brazil.
Antti PosoSchool of Pharmacy, University of Eastern Finland, Faculty of Health Sciences, Kuopio, 70211, Finland; Department of Medical Oncology and Pneumology, Internal Medicine VIII, University Hospital of Tübingen, Otfried-Müller-Strasse 14, 72076, Tübingen, Germany.
Robert W RobeyLaboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Suresh V AmbudkarLaboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Vivian Rotuno MourePharmaceutical Sciences Graduate Program, Laboratory of Cancer Drug Resistance, Federal University of Parana, Curitiba, PR, Brazil; Department of Clinical Analysis, Federal University of Parana, Curitiba, PR, Brazil.
Alan Guilherme GonçalvesDepartment of Pharmacy, Federal University of Parana, Curitiba, PR, Brazil. Electronic address: alan.goncalves@ufpr.br.
Glaucio ValdameriPharmaceutical Sciences Graduate Program, Laboratory of Cancer Drug Resistance, Federal University of Parana, Curitiba, PR, Brazil; Department of Clinical Analysis, Federal University of Parana, Curitiba, PR, Brazil. Electronic address: gvaldameri@ufpr.br.
Universidade Federal do Paraná · BRNational Institutes of Health · USUniversity of Eastern Finland · FIIndustrial University of Santander · COUniversidade Tecnológica Federal do Paraná · BR

Funding

Biochemical Analysis of Multidrug Resistance-linked Transport ProteinsZIABC010030 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI AMBUDKAR, SURESH · 2009 to 2025
$21.6M
Intramural NIH HHS ZIA BC010030
6 · The paper itself

Abstract

The ABCG2 transporter plays a pivotal role in multidrug resistance, however, no clinical trial using specific ABCG2 inhibitors have been successful. Although ABC transporters actively extrude a wide variety of substrates, photodynamic therapeutic agents with porphyrinic scaffolds are exclusively transported by ABCG2. In this work, we describe for the first time a porphyrin derivative (4B) inhibitor of ABCG2 and capable to overcome multidrug resistance in vitro. The inhibition was time-dependent and 4B was not itself transported by ABCG2. Independently of the substrate, the porphyrin 4B showed an IC

Indexed as

Adenosine TriphosphatasesATP Binding Cassette Transporter, Subfamily G, Member 2Cell Line, TumorDrug Evaluation, PreclinicalDrug Resistance, MultipleEnzyme InhibitorsHEK293 CellsHumansIrinotecanMolecular Docking SimulationMolecular Dynamics SimulationMolecular StructureNeoplasm ProteinsPorphyrinsProtein BindingProtein ConformationABCG2 protein, humanAdenosine TriphosphatasesATP Binding Cassette Transporter, Subfamily G, Member 2Enzyme InhibitorsIrinotecanNeoplasm ProteinsPorphyrinsABCG2 inhibitorABC transporterCancerMultidrug resistance

Identifiers

PMID34717915
PMCPMC10263179
OpenAlexW3209248260

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.