Evidence map›Paper›PMID 18699730›Full record

ReviewAntioxidants & redox signaling2009

Redox regulation of multidrug resistance in cancer chemotherapy: molecular mechanisms and therapeutic opportunities.

Macus Tien Kuo

Abstract readReview
In one paragraph

Review in Antioxidants & redox signaling, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
–field-weighted citation impact
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

54 citing papers in PubMed.

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  14. A NovelLife (Basel, Switzerland) · 2021
    Review
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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

1 author.

Macus Tien KuoDepartment of Molecular Pathology (Unit 951), The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA. tkuo@mdanderson.org

Funding

Genomic Instability and Evolution of Drug ResistanceR01CA089541 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KUO, MACUS T · 2004 to 2008
$1.4M
Redox Regulation of Multidrug Resistance Gene ExpressionR01CA079085 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KUO, MACUS T · 1999 to 2009
$1.3M
REGULATION OF MDR GENE EXPRESSION IN LIVER CANCERSR01CA072404 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI KUO, MACUS T · 1997 to 2004
$1.2M
NCI NIH HHS CA72404NCI NIH HHS CA79085NCI NIH HHS R01 CA079085NCI NIH HHS R01 CA089541
6 · The paper itself

Abstract

The development of multidrug resistance to cancer chemotherapy is a major obstacle to the effective treatment of human malignancies. It has been established that membrane proteins, notably multidrug resistance (MDR), multidrug resistance protein (MRP), and breast cancer resistance protein (BCRP) of the ATP binding cassette (ABC) transporter family encoding efflux pumps, play important roles in the development of multidrug resistance. Overexpression of these transporters has been observed frequently in many types of human malignancies and correlated with poor responses to chemotherapeutic agents. Evidence has accumulated showing that redox signals are activated in response to drug treatments that affect the expression and activity of these transporters by multiple mechanisms, including (a) conformational changes in the transporters, (b) regulation of the biosynthesis cofactors required for the transporter's function, (c) regulation of the expression of transporters at transcriptional, posttranscriptional, and epigenetic levels, and (d) amplification of the copy number of genes encoding these transporters. This review describes various specific factors and their relevant signaling pathways that are involved in the regulation. Finally, the roles of redox signaling in the maintenance and evolution of cancer stem cells and their implications in the development of intrinsic and acquired multidrug resistance in cancer chemotherapy are discussed.

Indexed as

AnimalsAntineoplastic AgentsATP-Binding Cassette, Sub-Family C ProteinsDrug Resistance, MultipleDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticGenes, MDRHumansModels, BiologicalNeoplasm ProteinsNeoplasmsOxidation-ReductionAntineoplastic AgentsATP-Binding Cassette, Sub-Family C ProteinsNeoplasm Proteins

Identifiers

PMID18699730
PMCPMC2577715

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.