Evidence map›Paper›PMID 23137650›Full record

ArticleExperimental cell research2013

Contributions of microRNA dysregulation to cisplatin resistance in adenocarcinoma cells.

Lynn M Pouliot, Ding-Wu Shen, Toshihiro Suzuki, Matthew D Hall, Michael M Gottesman

Abstract read
In one paragraph

Article in Experimental cell research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Molecular mechanisms of cisplatin resistance in cervical cancer.Drug design, development and therapy · 2016
    Review
  10. Epigenetics of lung cancer.Translational research : the journal of laboratory and clinical medicine · 2015
    Review
  11. A three-microRNA signature predicts responses to platinum-based doublet chemotherapy in patients with lung adenocarcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2014
    Article
  12. MicroRNAs: master regulators of drug resistance, stemness, and metastasis.Journal of molecular medicine (Berlin, Germany) · 2014
    Review
  13. Article
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 4 institutions in 2 countries.

Lynn M PouliotDepartment of Microbiology and Immunology, Georgetown University, Washington, DC, USA.
Ding-Wu Shen
Toshihiro Suzuki
Matthew D Hall
Michael M Gottesman
National Institutes of Health · USGeorgetown University · USMeiji Pharmaceutical University · JPNational Cancer Institute · US

Funding

Mechanisms of non-classical multidrug resistance in cancerZIABC010830 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GOTTESMAN, MICHAEL · 2009 to 2025
$19.6M
Genetic Analysis of the Multidrug Resistance Phenotype in Tumor CellsZIABC005598 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GOTTESMAN, MICHAEL · 2009 to 2025
$11.9M
Intramural NIH HHS ZIA BC005598Intramural NIH HHS ZIA BC010830
6 · The paper itself

Abstract

Cisplatin resistance in cancer cells is due to a pleiotropic phenotype transition that allows cells to resist cell death. miRNAs have been shown to be reliable markers of phenotype, critical in cell differentiation, and dysregulated in cancer and other pathologies. Here we investigate the influence of miRNA on cisplatin resistance in KB adenocarcinoma cells. Silencing both DICER and TRBP2 in the miRNA biosynthesis pathway in KB-3-1 (sensitive parental), KB-CP.5 (cisplatin-resistant), and KB-CP20 (highly cisplatin-resistant) cells resulted in the reversal of cisplatin resistance, with no effect on cell viability in the absence of cisplatin. We found miR-181 expression differences in the cell lines using RT-PCR, with several members of the miR-181 family overexpressed in two KB cisplatin-resistant lines and in two cisplatin-resistant lung cancer lines, compared to their respective parental cells. Functional assays showed minimal effects of miR-181 on cisplatin resistance. We conclude that the miRNA biosynthesis pathway is critical for maintaining the cisplatin-resistant phenotype, but that it is difficult to determine the precise miRNAs involved in cisplatin resistance simply using expression profiles of individual miRNA species. Functional assays are needed to determine the influence of a specific miRNA and different members of the same miRNA family may have opposite effects.

Indexed as

AdenocarcinomaAntineoplastic AgentsCell Line, TumorCisplatinDEAD-box RNA HelicasesDrug Evaluation, PreclinicalDrug Resistance, NeoplasmDrug SynergismFemaleGene Expression Regulation, NeoplasticHeLa CellsHumansMicroRNAsRibonuclease IIIRNA-Binding ProteinsRNA, Small InterferingAntineoplastic AgentsCisplatinDEAD-box RNA HelicasesDICER1 protein, humanMicroRNAsRibonuclease IIIRNA-Binding ProteinsRNA, Small InterferingTrans-Activation Responsive RNA-Binding Protein

Identifiers

PMID23137650
PMCPMC3563763
OpenAlexW1975096107

What OpenQuestion holds

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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.