Evidence map›Paper›PMID 25361006›Full record

ArticleOncotarget2014

Down-regulation of miRNA-106b inhibits growth of melanoma cells by promoting G1-phase cell cycle arrest and reactivation of p21/WAF1/Cip1 protein.

Ram Prasad, Santosh K Katiyar

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
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  13. MicroRNA-5110 regulates pigmentation by cotargeting melanophilin and WNT family member 1.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  14. Article
  15. Serum miR-106b upregulation predicts poor prognosis in patients with colorectal cancer.International journal of clinical and experimental pathology · 2018
    Article
  16. MicroRNA-Directed Cancer Therapies: Implications in Melanoma Intervention.The Journal of pharmacology and experimental therapeutics · 2018
    Review
  17. Article
  18. 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

2 authors at 2 institutions in 1 country.

Ram PrasadDepartment of Dermatology, University of Alabama at Birmingham, Birmingham, AL, USA.
Santosh K KatiyarDepartment of Dermatology, University of Alabama at Birmingham, Birmingham, AL, USA. Environmental Health Sciences, University of Alabama at Birmingham, Birmingham, AL, USA. Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA. Birmingham Veterans Affairs Medical Center, Birmingham, AL, USA.
Birmingham VA Medical Center · USUniversity of Alabama at Birmingham · US

Funding

UAB Skin Diseases Research CenterP30AR050948 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ELMETS, CRAIG A · 2004 to 2013
$5.5M
Proanthocyanidins,Novel bioactive components for prevention of melanoma invasionR21CA166883 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KATIYAR, SANTOSH KUMAR · 2013 to 2014
$346k
Prevention of photocarcinogenesis by dietary immunomodulationI01BX001410 · VA · BIRMINGHAM VA MEDICAL CENTER · PI KATIYAR, SANTOSH KUMAR · 2012 to 2015
–
BLRD VA I01 BX001410NCI NIH HHS CA166883NCI NIH HHS R21 CA166883NIAMS NIH HHS AR050948NIAMS NIH HHS P30 AR050948
6 · The paper itself

Abstract

MiR-106b is overexpressed in various types of cancers and is associated with the regulation of the carcinogenic processes. Using RT-PCR, we have identified overexpression of miRNA-106b in various melanoma cell lines (A375, Hs294t, SK-Mel28, SK-Mel 119, Mel 1241, Mel 1011 and Mel 928) as compared to its expression in normal human epidermal melanocytes (NHEM). The overexpression of miR-106b in melanoma cells (A375, Hs294t) was associated with greater cell proliferation capacity than NHEM. Treatment of A375 and Hs294t cells with anti-miR-106b resulted in inhibition of cell proliferation as well as G1-phase arrest. We determined the effects of grape seed proanthocyanidins (GSPs) on the expression of miRNA-106b and its underlying molecular targets. Treatment of A375 and Hs294t cells with GSPs resulted in suppression of the levels of miRNA-106b, cytotoxicity, G1-phase arrest and reactivation of p21/WAF1/Cip1. Dietary GSPs significantly inhibited growth of A375 melanoma cell tumor xenografts in nude mice, which was associated with reduction in the levels of miRNA-106b, tumor cell proliferation and increases in the levels of p21/WAF1/Cip1 protein. These studies suggest that miRNA-106b plays a crucial role in melanoma growth and that GSPs act as an inhibitor of miR-106b thereby blocking melanoma growth in vitro and in vivo models.

Indexed as

Cell ProliferationG1 Phase Cell Cycle CheckpointsAnimalsApoptosisBlotting, WesternCell CycleCyclin-Dependent Kinase Inhibitor p21Down-RegulationFemaleFlow CytometryGrape Seed ExtractHumansImmunoenzyme TechniquesIn Situ Hybridization, FluorescenceMelanomaMiceCyclin-Dependent Kinase Inhibitor p21Grape Seed ExtractGrape Seed ProanthocyanidinsMicroRNAsMIRN106 microRNA, humanProanthocyanidinsRNA, MessengerTumor Suppressor Protein p53

Identifiers

PMID25361006
PMCPMC4279399
OpenAlexW2141301290

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.