Evidence map›Paper›PMID 31176655›Full record

ArticleToxicology and applied pharmacology2019

Overexpression of hsa-miR-186 induces chromosomal instability in arsenic-exposed human keratinocytes.

Jiguo Wu, Ana P Ferragut Cardoso, Vanessa A R States, Laila Al-Eryani, Mark Doll, Sandra S Wise, Shesh N Rai, J Christopher States

Open access · greenAbstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  5. Article
  6. Article
  7. Article
  8. Review
  9. miR-186 induces tetraploidy in arsenic exposed human keratinocytes.Ecotoxicology and environmental safety · 2023
    Article
  10. Arsenic and cancer: Evidence and mechanisms.Advances in pharmacology (San Diego, Calif.) · 2023
    Article
  11. The Role of Non-Coding RNAs in Chromosomal Instability in Cancer.The Journal of pharmacology and experimental therapeutics · 2023
    Review
  12. Review
  13. Review
  14. Review
  15. Arsenic-Induced Carcinogenesis and Immune Dysregulation.International journal of environmental research and public health · 2019
    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

8 authors at 1 institution in 2 countries.

Jiguo WuDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA; Department of Environmental Health Science, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou 510515, China.
Ana P Ferragut CardosoDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA.
Vanessa A R StatesDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA.
Laila Al-EryaniDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA.
Mark DollDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA.
Sandra S WiseDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA.
Shesh N RaiBiostatisitcs and Bioinformatics Shared Facility, JGB Cancer Center and Department of Bioinformatics and Biostatistics, University of Louisville, Louisville, KY 40292, USA.
J Christopher StatesDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA. Electronic address: jcstates@louisville.edu.
University of Louisville · US

Funding

Mechanism for arsenic induced carcinogenesisR01ES027778 · NIEHS · UNIVERSITY OF LOUISVILLE · PI J CHRISTOPHER STATES · 2017 to 2026
$4.3M
Differential miRNA expression & progression of arsenic induced skin cancersR21ES023627 · NIEHS · UNIVERSITY OF LOUISVILLE · PI STATES, J CHRISTOPHER · 2015 to 2016
$422k
NIEHS NIH HHS R01 ES027778NIEHS NIH HHS R21 ES023627
6 · The paper itself

Abstract

The mechanism of arsenic-induced skin carcinogenesis is not yet fully understood. Chromosomal instability contributes to aneuploidy and is a driving force in carcinogenesis. Arsenic causes mitotic arrest and induces aneuploidy. hsa-miR-186 overexpression is associated with metastatic cancers as well as arsenic-induced squamous cell carcinoma and is reported to target several mitotic regulators. Decreased levels of these proteins can dysregulate chromatid segregation contributing to aneuploidy. This work investigates the potential aneuploidogenic role of hsa-miR-186 in arsenic carcinogenesis. Clones of immortalized human keratinocytes (HaCaT) stably transfected with a hsa-miR-186 expression or empty vector were isolated. Three clones with high and low hsa-miR-186 expression determined by RT-qPCR were selected for further analysis and cultured with 0 or 100 nM NaAsO

Indexed as

ArsenicArsenitesCarcinogenesisCell LineChromosomal InstabilityHumansKeratinocytesMicroRNAsArsenicarseniteArsenitesMicroRNAsMIRN186 microRNA, humanArsenicCarcinogenesisChromosomal InstabilityKeratinocytesmiR-186Skin Cancer

Identifiers

PMID31176655
PMCPMC6746570
OpenAlexW2954285789

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.