Evidence map›Paper›PMID 31292714›Full record

ReviewJournal of cancer research and clinical oncology2019

Models used to screen for the treatment of multidrug resistant cancer facilitated by transporter-based efflux.

Clarissa Willers, Hanna Svitina, Michael J Rossouw, Roan A Swanepoel, Josias H Hamman, Chrisna Gouws

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cancer research and clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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 1 institution in 1 country.

Clarissa WillersPharmacen™, Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom, 2520, South Africa.ORCID http://orcid.org/0000-0003-2481-6998
Hanna SvitinaPharmacen™, Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom, 2520, South Africa.ORCID http://orcid.org/0000-0003-4811-3787
Michael J RossouwPharmacen™, Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom, 2520, South Africa.ORCID http://orcid.org/0000-0002-3401-8829
Roan A SwanepoelPharmacen™, Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom, 2520, South Africa.ORCID http://orcid.org/0000-0003-2280-6235
Josias H HammanPharmacen™, Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom, 2520, South Africa.ORCID http://orcid.org/0000-0002-8916-3927
Chrisna GouwsPharmacen™, Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom, 2520, South Africa. chrisna.gouws@nwu.ac.za.ORCID http://orcid.org/0000-0001-5747-8214
North-West University · ZA

Funding

National Research Foundation 115245National Research Foundation 91460National Research Foundation 98939South African Medical Research Council Self-initiated Research Grant
6 · The paper itself

Abstract

purposeEfflux transporters of the adenosine triphosphate-binding cassette (ABC)-superfamily play an important role in the development of multidrug resistance (multidrug resistant; MDR) in cancer. The overexpression of these transporters can directly contribute to the failure of chemotherapeutic drugs. Several in vitro and in vivo models exist to screen for the efficacy of chemotherapeutic drugs against MDR cancer, specifically facilitated by efflux transporters.

resultsThis article reviews a range of efflux transporter-based MDR models used to test the efficacy of compounds to overcome MDR in cancer. These models are classified as either in vitro or in vivo and are further categorised as the most basic, conventional models or more complex and advanced systems. Each model's origin, advantages and limitations, as well as specific efflux transporter-based MDR applications are discussed. Accordingly, future modifications to existing models or new research approaches are suggested to develop prototypes that closely resemble the true nature of multidrug resistant cancer in the human body.

conclusionsIt is evident from this review that a combination of both in vitro and in vivo preclinical models can provide a better understanding of cancer itself, than using a single model only. However, there is still a clear lack of progression of these models from basic research to high-throughput clinical practice.

Indexed as

Drug Resistance, MultipleDrug Resistance, NeoplasmModels, BiologicalAntineoplastic AgentsATP-Binding Cassette TransportersBiological TransportCulture TechniquesDecision Support TechniquesDrug Screening Assays, AntitumorHumansOrgan SpecificityPatient SelectionAntineoplastic AgentsATP-Binding Cassette TransportersCancerCell cultureEfflux transporterGenetically engineered mouse modelMultidrug resistancePreclinical screening model

Identifiers

PMID31292714
PMCPMC11810382
OpenAlexW2957484702

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.