Evidence map›Paper›PMID 30723145›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

Integrated Genomic and Functional microRNA Analysis Identifies miR-30-5p as a Tumor Suppressor and Potential Therapeutic Nanomedicine in Head and Neck Cancer.

Anthony D Saleh, Hui Cheng, Scott E Martin, Han Si, Pinar Ormanoglu, Sophie Carlson, Paul E Clavijo, Xinping Yang, Rita Das, Shaleeka Cornelius and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

51 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
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  9. Deregulation of All-International journal of molecular sciences · 2023
    Review
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  20. Dihydroartemisinin ameliorates chronic nonbacterial prostatitis and epithelial cellular inflammation by blocking the E2F7/HIF1α pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    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

26 authors at 11 institutions in 3 countries.

Anthony D SalehTumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland.
Hui ChengTumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland.
Scott E MartinRNAi Screening Facility, National Center for Advancing Translational Sciences, NIH, Bethesda, Maryland.
Han SiMolecular Characterization & Clinical Assay Development Laboratory, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, Maryland.
Pinar OrmanogluRNAi Screening Facility, National Center for Advancing Translational Sciences, NIH, Bethesda, Maryland.
Sophie CarlsonTumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland.
Paul E ClavijoTumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland.
Xinping YangTumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland.
Rita DasTumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland.
Shaleeka CorneliusTumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland.
Jamie CouperTumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland.
Douglas ChepehaDepartment of Otolaryngology-Head and Neck Surgery, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0001-9062-3719
Ludmila DanilovaDepartment of Medical Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0003-2813-3094
Thomas M HarrisDepartment of Pathology, Einstein School of Medicine, Bronx, New York.
Michael B PrystowskyDepartment of Pathology, Einstein School of Medicine, Bronx, New York.
Geoffrey J ChildsDepartment of Pathology, Einstein School of Medicine, Bronx, New York.
Richard V SmithDepartment of Otorhinolaryngology-Head and Neck Surgery, Montefiore Medical Center, Bronx, New York.
A Gordon RobertsonCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, British Columbia, Canada.ORCID 0000-0002-2839-596X
Steven J M JonesCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, British Columbia, Canada.ORCID 0000-0003-3394-2208
Andrew D CherniackCancer Program, Broad Institute of Harvard and MIT, Cambridge, Massachusetts.ORCID 0000-0003-0470-0111
Sang S KimDepartments of Oncology and Otolaryngology at the Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Georgetown, Washington DC.
Antonina RaitDepartments of Oncology and Otolaryngology at the Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Georgetown, Washington DC.
Kathleen F PirolloDepartments of Oncology and Otolaryngology at the Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Georgetown, Washington DC.
Esther H ChangDepartments of Oncology and Otolaryngology at the Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Georgetown, Washington DC.
Zhong ChenTumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland. vanwaesc@nidcd.nih.gov chenz@nidcd.nih.gov.
Carter Van WaesTumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland. vanwaesc@nidcd.nih.gov chenz@nidcd.nih.gov.
National Institute on Deafness and Other Communication Disorders · USGeorgetown University · USAlbert Einstein College of Medicine · USCanada's Michael Smith Genome Sciences Centre · CANational Center for Advancing Translational Sciences · USBroad Institute · USCASI Pharmaceuticals (United States) · USJohns Hopkins University · USLeidos (United States) · USMontefiore Medical Center · USUniversity of Michigan · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
Genomics and Proteomics of Head and Neck CancerZIADC000074 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI VAN WAES, CARTER · 2009 to 2022
$11.1M
Trans-NIH RNAi Facility (TNRF)ZICTR000041 · NCATS · NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES · PI CHENG, KEN · 2015 to 2025
$9.4M
NF-kappaB in pathogenesis and therapy of head and neck cancerZIADC000016 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI VAN WAES, CARTER · 2009 to 2022
$9.3M
Signal and Transcription Factor Network interactions in Head and Neck CancerZIADC000073 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI VAN WAES, CARTER · 2009 to 2022
$9.1M
Intramural NIH HHS ZIA DC000016Intramural NIH HHS ZIA DC000073Intramural NIH HHS ZIA DC000074NCI NIH HHS P30 CA006973
6 · The paper itself

Abstract

purposeTo identify deregulated and inhibitory miRNAs and generate novel mimics for replacement nanomedicine for head and neck squamous cell carcinomas (HNSCC). EXPERIMENTAL

designWe integrated miRNA and mRNA expression, copy number variation, and DNA methylation results from The Cancer Genome Atlas (TCGA), with a functional genome-wide screen.

resultsWe reveal that the miR-30 family is commonly repressed, and all 5 members sharing these seed sequence similarly inhibit HNSCC proliferation

conclusionsWe identify the miR-30 family as an important regulator of signal networks and tumor suppressor in a subset of HNSCC patients, which may benefit from miRNA replacement nanomedicine therapy.

Indexed as

Genes, Tumor SuppressorAnimalsApoptosisBiomarkers, TumorCase-Control StudiesCell MovementCell ProliferationDNA Copy Number VariationsFemaleFollow-Up StudiesGene Expression ProfilingGene Expression Regulation, NeoplasticGenomicsHead and Neck NeoplasmsHumansMiceBiomarkers, TumorMicroRNAsMIRN30b microRNA, human

Identifiers

PMID30723145
PMCPMC6497577
OpenAlexW2912476769

What OpenQuestion holds

Textmetadata
LicenceTDM
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.