Evidence map›Paper›PMID 17890317›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

MicroRNA-29 family reverts aberrant methylation in lung cancer by targeting DNA methyltransferases 3A and 3B.

Muller Fabbri, Ramiro Garzon, Amelia Cimmino, Zhongfa Liu, Nicola Zanesi, Elisa Callegari, Shujun Liu, Hansjuerg Alder, Stefan Costinean, Cecilia Fernandez-Cymering and 8 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02009852 (The Role of microRNA-29b in the Oral Squamous Cell Carcinoma), which is not on this map. Cited by 837 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
837citing papers in PubMed, 2 pooled it
34.2field-weighted citation impact, top 1% 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.

NCT02009852 unknown statusnot on this mapstarted 2014, after this paper: background citation

The Role of microRNA-29b in the Oral Squamous Cell Carcinoma

Typeobservational_patient_registrySponsorNational Taiwan University HospitalRan2014Enrolled100ConditionsOral Cancer
3 · Its place in the literature

Who cites it

837 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,655 citations in OpenAlex.

  1. Pooled it
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  4. Tuning epigenetics to enhance cancer virotherapy.Acta pharmaceutica Sinica. B · 2026
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777 more citing papers are in PubMed but not listed here.

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

18 authors at 5 institutions in 3 countries.

Muller FabbriDepartment of Molecular Virology, Immunology, and Medical Genetics, Comprehensive Cancer Center, and College of Pharmacy, Ohio State University, Columbus, OH 43210, USA.
Ramiro Garzon
Amelia Cimmino
Zhongfa Liu
Nicola Zanesi
Elisa Callegari
Shujun Liu
Hansjuerg Alder
Stefan Costinean
Cecilia Fernandez-Cymering
Stefano Volinia
Gulnur Guler
Carl D Morrison
Kenneth K Chan
Guido Marcucci
George A Calin
Kay Huebner
Carlo M Croce
The Ohio State University · USComprehensive Blood & Cancer Center · USHacettepe University · TRRoswell Park Comprehensive Cancer Center · USUniversity of Campania "Luigi Vanvitelli" · IT

Funding

Wwox as a Critical Signal Mediator in Breast CancerR01CA120516 · NCI · OHIO STATE UNIVERSITY · PI HUEBNER, KAY · 2006 to 2013
$1.3M
Fhit modulation of cell cycle progression and DNA damage responseR01CA132453 · NCI · OHIO STATE UNIVERSITY · PI HUEBNER, KAY · 2007 to 2010
$1.3M
NCI NIH HHS R01 CA120516NCI NIH HHS R01 CA132453
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small, noncoding RNAs that regulate expression of many genes. Recent studies suggest roles of miRNAs in carcinogenesis. We and others have shown that expression profiles of miRNAs are different in lung cancer vs. normal lung, although the significance of this aberrant expression is poorly understood. Among the reported down-regulated miRNAs in lung cancer, the miRNA (miR)-29 family (29a, 29b, and 29c) has intriguing complementarities to the 3'-UTRs of DNA methyltransferase (DNMT)3A and -3B (de novo methyltransferases), two key enzymes involved in DNA methylation, that are frequently up-regulated in lung cancer and associated with poor prognosis. We investigated whether miR-29s could target DNMT3A and -B and whether restoration of miR-29s could normalize aberrant patterns of methylation in non-small-cell lung cancer. Here we show that expression of miR-29s is inversely correlated to DNMT3A and -3B in lung cancer tissues, and that miR-29s directly target both DNMT3A and -3B. The enforced expression of miR-29s in lung cancer cell lines restores normal patterns of DNA methylation, induces reexpression of methylation-silenced tumor suppressor genes, such as FHIT and WWOX, and inhibits tumorigenicity in vitro and in vivo. These findings support a role of miR-29s in epigenetic normalization of NSCLC, providing a rationale for the development of miRNA-based strategies for the treatment of lung cancer.

Indexed as

DNA MethylationCarcinoma, Non-Small-Cell LungDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNA Methyltransferase 3BDNA, NeoplasmGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHumansLungLung NeoplasmsMicroRNAsPrognosisRNA, NeoplasmSurvival AnalysisDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNA Methyltransferase 3BDNA, NeoplasmDNMT3A protein, humanMicroRNAsRNA, Neoplasm

Identifiers

PMID17890317
PMCPMC2000384
OpenAlexW2103177465

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.