Evidence map›Paper›PMID 24650256›Full record

ArticleJournal of biomedical science2014

SNP rs10248565 in HDAC9 as a novel genomic aberration biomarker of lung adenocarcinoma in non-smoking women.

Liang-Chuan Lai, Mong-Hsun Tsai, Pei-Chun Chen, Lee H Chen, Jen-Hao Hsiao, Shin-Kuang Chen, Tzu-Pin Lu, Jang-Ming Lee, Chung-Ping Hsu, Chuhsing K Hsiao and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of biomedical science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

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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 4 institutions in 1 country.

Liang-Chuan LaiGraduate Institute of Physiology, National Taiwan University, Taipei, Taiwan. llai@ntu.edu.tw.
Mong-Hsun Tsai
Pei-Chun Chen
Lee H Chen
Jen-Hao Hsiao
Shin-Kuang Chen
Tzu-Pin Lu
Jang-Ming Lee
Chung-Ping Hsu
Chuhsing K Hsiao
Eric Y Chuang
National Taiwan University · TWNational Taiwan University Hospital · TWProvidence University · TWTaichung Veterans General Hospital · TW

Funding

ORGANIZATION AND FUNCTIONS OF CELLULAR STRUCTUREST32GM007184 · NIGMS · DUKE UNIVERSITY · PI JINKS-ROBERTSON, SUE · 1985 to 2019
$18.2M
NIGMS NIH HHS T32 GM007184
6 · The paper itself

Abstract

backgroundNumerous efforts have been made to elucidate the etiology and improve the treatment of lung cancer, but the overall five-year survival rate is still only 15%. Although cigarette smoking is the primary risk factor for lung cancer, only 7% of female lung cancer patients in Taiwan have a history of smoking. Since cancer results from progressive accumulation of genetic aberrations, genomic rearrangements may be early events in carcinogenesis.

resultsIn order to identify biomarkers of early-stage adenocarcinoma, the genome-wide DNA aberrations of 60 pairs of lung adenocarcinoma and adjacent normal lung tissue in non-smoking women were examined using Affymetrix Genome-Wide Human SNP 6.0 arrays. Common copy number variation (CNV) regions were identified by ≥30% of patients with copy number beyond 2 ± 0.5 of copy numbers for each single nucleotide polymorphism (SNP) and at least 100 continuous SNP variant loci. SNPs associated with lung adenocarcinoma were identified by McNemar's test. Loss of heterozygosity (LOH) SNPs were identified in ≥18% of patients with LOH in the locus. Aberration of SNP rs10248565 at HDAC9 in chromosome 7p21.1 was identified from concurrent analyses of CNVs, SNPs, and LOH.

conclusionThe results elucidate the genetic etiology of lung adenocarcinoma by demonstrating that SNP rs10248565 may be a potential biomarker of cancer susceptibility.

Indexed as

Genome-Wide Association StudyAdenocarcinomaAdenocarcinoma of LungAgedFemaleGenetic Predisposition to DiseaseGenome, HumanHistone DeacetylasesHumansLoss of HeterozygosityLung NeoplasmsMicroarray AnalysisMiddle AgedPolymorphism, Single NucleotideRepressor ProteinsSmokingHDAC9 protein, humanHistone DeacetylasesRepressor Proteins

Identifiers

PMID24650256
PMCPMC3994426
OpenAlexW2155602190

What OpenQuestion holds

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LicenceCC BY
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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.