Evidence map›Paper›PMID 33616835›Full record

ReviewMolecular biology reports2021

ABC transporter superfamily. An updated overview, relevance in cancer multidrug resistance and perspectives with personalized medicine.

Pérez-De Marcos Juan-Carlos, Pérez-Pineda Perla-Lidia, Méndez-Morales Stephanie-Talia, Arellano-Mendoza Mónica-Griselda, Torres-Espíndola Luz-María

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
6.3field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 77 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

5 authors at 2 institutions in 2 countries.

Pérez-De Marcos Juan-CarlosLaboratory of Pharmacology, National Institute of Pediatrics, Mexico City, México.ORCID https://orcid.org/0000-0003-4634-8267
Pérez-Pineda Perla-LidiaLaboratory of Pharmacology, National Institute of Pediatrics, Mexico City, México.ORCID https://orcid.org/0000-0001-9902-4376
Méndez-Morales Stephanie-TaliaLaboratory of Chronic-Degenerative Diseases, National Polytechnic Institute, Mexico City, México.ORCID https://orcid.org/0000-0002-6500-3224
Arellano-Mendoza Mónica-GriseldaLaboratory of Chronic-Degenerative Diseases, National Polytechnic Institute, Mexico City, México.ORCID https://orcid.org/0000-0003-2462-4363
Torres-Espíndola Luz-MaríaLaboratory of Pharmacology, National Institute of Pediatrics, Mexico City, México. luzmtorres@gmail.com.ORCID http://orcid.org/0000-0001-9929-9361
Tecnológico Nacional de México · MXVietnam National Children's Hospital · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ATP binding-cassette superfamily corresponds the mostly transmembrane transporters family found in humans. These proteins actively transport endogenous and exogenous substrates through biological membranes in body tissues, so they have an important role in the regulation of many physiological functions necessary for human homeostasis, as well as in response regulation to several pharmacological substrates. The development of multidrug resistance has become one of the main troubles in conventional chemotherapy in different illnesses including cancer, being the increased efflux of antineoplastic drugs the main reason for this multidrug resistance, with a key role of the ABC superfamily. Likely, the interindividual variability in the pharmacological response among patients is well known, and may be due to intrinsically factors of the disease, genetic and environmental ones. Thus, the understanding of this variability, especially the genetic variability associated with the efficacy and toxicity of drugs, can provide a safer and more effective pharmacological treatment, so ABC genes are considered as important regulators due to their relationship with the reduction in pharmacological response. In this review, updated information about transporters belonging to this superfamily was collected, the possible role of these transporters in cancer, the role of genetic variability in their genes, as well as some therapeutic tools that have been tried to raise against main transporters associated with chemoresistance in cancer.

Indexed as

Antineoplastic AgentsATP-Binding Cassette TransportersDrug Resistance, MultipleDrug Resistance, NeoplasmHumansNeoplasmsPharmacogeneticsPrecision MedicineAntineoplastic AgentsATP-Binding Cassette TransportersABC transportersCancerMolecular biologyMultidrug resistancePersonalized medicinePharmacogenomics

Identifiers

PMID33616835
OpenAlexW3130681257

What OpenQuestion holds

Textmetadata
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.