Evidence map›Paper›PMID 25764126›Full record

ArticlePloS one2015

Functions of MiRNA-128 on the regulation of head and neck squamous cell carcinoma growth and apoptosis.

Belinda Hauser, Yuan Zhao, Xiaowu Pang, Zhiqiang Ling, Ernest Myers, Paul Wang, Joseph Califano, Xinbin Gu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.3field-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

29 citing papers in PubMed, 48 citations in OpenAlex.

  1. Expression ofInternational journal of molecular sciences · 2026
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  5. miRNA in head and neck squamous cell carcinomas: promising but still distant future of personalized oncology.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2023
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  17. MiRNA373 induces cervical squamous cell carcinoma SiHa cell apoptosis.Cancer biomarkers : section A of Disease markers · 2018
    Article
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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

8 authors at 2 institutions in 1 country.

Belinda HauserDepartment of Genetics and Human Genetics, Howard University, Washington, DC, United States of America.
Yuan ZhaoDepartment of Oral Pathology, Howard University, Washington DC, United States of America.
Xiaowu PangDepartment of Oral Pathology, Howard University, Washington DC, United States of America.
Zhiqiang LingZhejiang Cancer Research Institute, Hangzhou, China.
Ernest MyersDepartment of Otolaryngology-Head and Neck Surgery, Howard University, Washington, DC, United States of America.
Paul WangDepartment of Radiology, Howard University, Washington DC, United States of America; Cancer Center, Howard University, Washington, District of Columbia, United States of America.
Joseph CalifanoDepartments of Otolaryngology-Head and Neck Surgery, and Head & Neck Research Division, Johns Hopkins University, Baltimore, Maryland, United states of America.
Xinbin GuDepartment of Genetics and Human Genetics, Howard University, Washington, DC, United States of America; Department of Oral Pathology, Howard University, Washington DC, United States of America; Cancer Center, Howard University, Washington, District of Columbia, United States of America.
Howard University · USJohns Hopkins University · US

Funding

STRUCTURAL/FUNCTIONAL CHARACTERIZATION OF AMINOGLYCOSIDEG12RR003048 · NCRR · HOWARD UNIVERSITY · PI SOUTHERLAND, WILLIAM M. · 1985 to 2011
$19.0M
PROTEOMICS CORE FACILITYG12MD007597 · NIMHD · HOWARD UNIVERSITY · PI SOUTHERLAND, WILLIAM M. · 2012 to 2018
$14.8M
Train-Edu-Prog, Collaborative Cancer Research Training and Education Program Leading to Minority InitiativeP20CA192989 · NCI · HOWARD UNIVERSITY · PI GU, XINBIN · 2014 to 2017
$801k
HU/JHU Head and Neck Cancer Translational Research and *P20CA118770 · NCI · HOWARD UNIVERSITY · PI GU, XINBIN · 2005 to 2008
$793k
NCI NIH HHS CA192989-01NCI NIH HHS P20 CA118770NCI NIH HHS P20 CA192989NCRR NIH HHS 2G12RR003048NCRR NIH HHS G12 RR003048NIMHD NIH HHS G12 MD007597
6 · The paper itself

Abstract

backgroundIncidence of head and neck squamous cell carcinoma (HNSCC) has continuously increased in past years while its survival rate has not been significantly improved. There is a critical need to better understand the genetic regulation of HNSCC tumorigenesis and progression. In this study, we comprehensively analyzed the function of miRNA-128 (miR-128) in the regulation of HNSCC growth and its putative targets in vitro and in vivo systems.

methodsThe function and targets of miR-128 were investigated in human HNSCC cell lines (JHU-13 and JHU-22), which were stably transfected with the miR-128 gene using a lentiviral delivery system. The expression levels of miR-128 and its targeted proteins were analyzed with qRT-PCR, Western blotting and flow cytometry. The binding capacity of miRNA-128 to its putative targets was determined using a luciferase report assay. MTT, colony formation, and a tumor xenograft model further evaluated the effects of miR-128 on HNSCC growth.

resultsWe generated two miR-128 stably transfected human HNSCC cell lines (JHU-13miR-128 and JHU-22miR-128). Enforced expression of miR-128 was detected in both cultured JHU-13miR-128 and JHU-22miR-128 cell lines, approximately seventeen to twenty folds higher than in vector control cell lines. miRNA-128 was able to bind with the 3'-untranslated regions of BMI-1, BAG-2, BAX, H3f3b, and Paip2 mRNAs, resulting in significant reduction of the targeted protein levels. We found that upregulated miR-128 expression significantly inhibited both JHU-13miR-128 and JHU-22miR-128 cell viability approximately 20 to 40%, and the JHU-22miR-128 tumor xenograft growth compared to the vector control groups.

conclusionsmiR-128 acted as a tumor suppressor inhibiting the HNSCC growth by directly mediating the expression of putative targets. Our results provide a better understanding of miRNA-128 function and its potential targets, which may be valuable for developing novel diagnostic markers and targeted therapy.

Indexed as

AnimalsApoptosisbcl-2-Associated X ProteinCarcinoma, Squamous CellCell Line, TumorCell ProliferationHead and Neck NeoplasmsHumansMaleMiceMice, NudeMicroRNAsMolecular ChaperonesNeoplasm TransplantationPolycomb Repressive Complex 1Repressor ProteinsBAG2 protein, humanBAX protein, humanbcl-2-Associated X ProteinBMI1 protein, humanMicroRNAsMIRN128 microRNA, humanMolecular ChaperonesPAIP2 protein, humanPolycomb Repressive Complex 1Repressor ProteinsRNA-Binding Proteins

Identifiers

PMID25764126
PMCPMC4357443
OpenAlexW2020926751

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.