Evidence map›Paper›PMID 16756719›Full record

ArticleNeoplasia (New York, N.Y.)2006

Candidate tumor-suppressor gene DLEC1 is frequently downregulated by promoter hypermethylation and histone hypoacetylation in human epithelial ovarian cancer.

Joseph Kwong, Ji-Young Lee, Kwong-Kwok Wong, Xiaofeng Zhou, David T W Wong, Kwok-Wai Lo, William R Welch, Ross S Berkowitz, Samuel C Mok

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
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  3. PMEnvironmental health and preventive medicine · 2020
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  11. Experimental and therapeutic medicine · 2016
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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

9 authors at 5 institutions in 2 countries.

Joseph KwongLaboratory of Gynecologic Oncology, Division of Gynecology Oncology, Department of Obstetrics, Gynecology, and Reproductive Biology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA. jkwong@rics.bwh.harvard.edu
Ji-Young Lee
Kwong-Kwok Wong
Xiaofeng Zhou
David T W Wong
Kwok-Wai Lo
William R Welch
Ross S Berkowitz
Samuel C Mok
Brigham and Women's Hospital · USHarvard University Press · USUniversity of California, Los Angeles · USPrince of Wales Hospital · CNThe University of Texas MD Anderson Cancer Center · US

Funding

Prognostic markers for ovarian cancerR33CA103595 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MOK, SAMUEL C · 2003 to 2006
$1.8M
Genomic Predictors of Oral Premalignancy ProgressionK22DE014847 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ZHOU, XIAOFENG · 2004 to 2009
$619k
NCI NIH HHS P50CA165009NCI NIH HHS R33 CA103595NCI NIH HHS R33CA103595NIDCR NIH HHS K22 DE014847NIDCR NIH HHS K22DE014847
6 · The paper itself

Abstract

Suppression of ovarian tumor growth by chromosome 3p was demonstrated in a previous study. Deleted in Lung and Esophageal Cancer 1 (DLEC1) on 3p22.3 is a candidate tumor suppressor in lung, esophageal, and renal cancers. The potential involvement of DLEC1 in epithelial ovarian cancer remains unknown. In the present study, DLEC1 downregulation was found in ovarian cancer cell lines and primary ovarian tumors. Focus-expressed DLEC1 in two ovarian cancer cell lines resulted in 41% to 52% inhibition of colony formation. No chromosomal loss of chromosome 3p22.3 in any ovarian cancer cell line or tissue was found. Promoter hypermethylation of DLEC1 was detected in ovarian cancer cell lines with reduced DLEC1 transcripts, whereas methylation was not detected in normal ovarian epithelium and DLEC1-expressing ovarian cancer cell lines. Treatment with demethylating agent enhanced DLEC1 expression in 90% (9 of 10) of ovarian cancer cell lines. DLEC1 promoter methylation was examined in 13 high-grade ovarian tumor tissues with DLEC1 downregulation, in which 54% of the tumors showed DLEC1 methylation. In addition, 80% of ovarian cancer cell lines significantly upregulated DLEC1 transcripts after histone deacetylase inhibitor treatment. Therefore, our results suggested that DLEC1 suppressed the growth of ovarian cancer cells and that its downregulation was closely associated with promoter hypermethylation and histone hypoacetylation.

Indexed as

Gene Expression Regulation, NeoplasticHistone Deacetylase InhibitorsPromoter Regions, GeneticCell Line, TumorDNA MethylationEnzyme InhibitorsFemaleHistonesHumansLoss of HeterozygosityOvarian NeoplasmsTumor Suppressor ProteinsUp-RegulationDLEC1 protein, humanEnzyme InhibitorsHistone Deacetylase InhibitorsHistonesTumor Suppressor Proteins

Identifiers

PMID16756719
PMCPMC1600675
OpenAlexW1966490076

What OpenQuestion holds

Textmetadata
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.