Evidence map›Paper›PMID 30289952›Full record

ArticlePloS one2018

Smoking-induced control of miR-133a-3p alters the expression of EGFR and HuR in HPV-infected oropharyngeal cancer.

Reniqua House, Mrinmoyee Majumder, Harinarayan Janakiraman, Besim Ogretmen, Masanari Kato, Evren Erkul, Elizabeth Hill, Carl Atkinson, Jeremy Barth, Terrence A Day and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 25% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

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  10. Biomedicines · 2021
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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

11 authors at 2 institutions in 2 countries.

Reniqua HouseDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Mrinmoyee MajumderDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Harinarayan JanakiramanDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Besim OgretmenDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Masanari KatoStony Brook University School of Medicine, Stony Brook, NY, United States of America.
Evren ErkulDepartment of Otolaryngology and Head and Neck Surgery, College of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Elizabeth HillDepartment of Public Health Sciences, College of Medicine, Medical University of South Carolina, Charleston, United States of America.
Carl AtkinsonDepartment of Microbiology & Immunology, College of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Jeremy BarthDepartment of Regenerative Medicine & Cell Biology, College of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Terrence A DayStony Brook University School of Medicine, Stony Brook, NY, United States of America.
Viswanathan PalanisamyDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.ORCID 0000-0001-5128-2878
Medical University of South Carolina · USStony Brook University · US

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
Project 3: Targeting SK2/S1P Signaling for the Regulation of c-Myc and Tumor SuppressionP01CA203628 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI OGRETMEN, BESIM · 2016 to 2021
$8.9M
Ceramide Signaling in the Regulation of Head & Neck Cancer Cell Death and TherapyR01DE016572 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI OGRETMEN, BESIM · 2005 to 2025
$7.4M
Pilot and Feasibility Project ProgramP30GM103331 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI WESTWATER, CAROLINE · 2012 to 2016
$5.2M
Mechanisms Of RNA-Binding Protein-Mediated Apoptosis In Oral MucositisR01DE022776 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PALANISAMY, VISWANATHAN · 2013 to 2017
$2.1M
Comprehensive Identification of FXR1 Targets Using pSILAC-BONCAT ProteomicsR21DE025920 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PALANISAMY, VISWANATHAN · 2017 to 2018
$411k
NCATS NIH HHS UL1 TR001450NCI NIH HHS P01 CA203628NIDCR NIH HHS R01 DE016572NIDCR NIH HHS R01 DE022776NIDCR NIH HHS R21 DE025920NIGMS NIH HHS P30 GM103331
6 · The paper itself

Abstract

purposeHuman papillomavirus (HPV) infected oropharyngeal squamous cell carcinoma (OPSCC) patients have a better prognosis compared to HPV(-) counterparts. However, a subset of HPV(+) patients with a smoking history fail to respond to the standard of care treatments such as radiation and chemotherapy. To understand the underlying mechanism driving HPV(+) OPSCC patient resistance to treatment and recurrence, we sought to identify and characterize the differentially expressed miRNAs and their target genes in HPV(+) smokers and non-smokers. EXPERIMENTAL

designMicroRNA expression analysis was performed using Nanostring in tumor tissues isolated from a prospective cohort of HPV(+) smoking (n = 9) and HPV(+) (n = 13) non-smoking OPSCC patients. Identified miRNAs of interest were further validated using qRT-PCR in cigarette smoke extract (CSE) treated HPV(+) and E6/E7 overexpressing HPV(-) cells.

resultsIn comparison to OPSCC HPV(+) non-smokers, 38 miRNAs were significantly altered in the HPV(+) smoker patients cohort and out of that 9 were downregulated. Altered miRNA expression was also detected in the serum and metastatic lymph nodes of HPV(+) smokers versus non-smokers. Expression of miR-133a-3p was significantly downregulated in OPSCC smokers, HPV(+) cells and E6/E7 overexpressing HPV(-) cells treated with CSE. Reduction of miR-133a-3p induced the upregulation of miR-133a-3p target mRNAs EGFR and HuR.

conclusionsOur results indicate that miR-133a-3p is a target of smoking-induced changes in HPV(+) patients and alters the expression of EGFR and HuR which may promote HPV associated oropharyngeal cancer. Therefore, future treatment strategies for HPV(+) OPSCC smokers should focus on EGFR inhibition and the development of selective therapies to target HuR.

Indexed as

AdultAgedCell Line, TumorCohort StudiesELAV-Like Protein 1ErbB ReceptorsFemaleGene Expression Regulation, NeoplasticHumansMaleMicroRNAsMiddle AgedOropharyngeal NeoplasmsPapillomaviridaePapillomavirus InfectionsProspective StudiesEGFR protein, humanELAVL1 protein, humanELAV-Like Protein 1ErbB ReceptorsMicroRNAsMIRN133 microRNA, humanRNA, MessengerTobacco Smoke Pollution

Identifiers

PMID30289952
PMCPMC6173415
OpenAlexW2894719749

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.