Evidence map›Paper›PMID 22468217›Full record

ArticleKorean journal of urology2012

DNA methylation of GSTP1 in human prostate tissues: pyrosequencing analysis.

Hyung-Yoon Yoon, Young-Won Kim, Ho-Won Kang, Won Tae Kim, Seok-Joong Yun, Sang-Cheol Lee, Wun-Jae Kim, Yong-June Kim

Abstract read
In one paragraph

Article in Korean journal of urology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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. Article
  2. Identification of a 24-gene panel and a novel marker ofComputational and structural biotechnology journal · 2023
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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Hyung-Yoon YoonDepartment of Urology, Chungbuk National University College of Medicine, Cheongju, Korea.
Young-Won Kim
Ho-Won Kang
Won Tae Kim
Seok-Joong Yun
Sang-Cheol Lee
Wun-Jae Kim
Yong-June Kim

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDNA methylation is an important epigenetic mechanism of gene regulation and plays essential roles in tumor initiation and progression. Differences in methylation patterns between neoplastic and normal cells can be used to detect the presence of cancer. The aim of the present study was to evaluate the usefulness of glutathione-S-transferase-Pi (GSTP1) hypermethylation in discriminating between normal and prostate cancer (PCa) cells and in predicting tumor characteristics by use of quantitative pyrosequencing analysis. MATERIALS AND

methodsA total of 100 human prostate tissues obtained from our institute were used in this study: 45 for benign prostatic hyperplasia (BPH) and 55 for PCa. The methylation level of GSTP1 was examined by a quantitative pyrosequencing analysis. The associations between GSTP1 methylation level and clinico-pathological parameter were also compared.

resultsThe level of GSTP1 methylation was significantly higher in PCa samples than in BPH samples (56.7±32.7% vs. 1.6±2.2%, p<0.001). The sensitivity and specificity of GSTP1 methylation status in discriminating between PCa and BPH reached 85.5% and 100%, respectively. Even after stratification by stage, Gleason score, and prostate-specific antigen (PSA) level, similar results were obtained. A positive correlation between GSTP1 methylation level and serum PSA level was observed (r=0.303, p=0.002). There were no associations between GSTP1 methylation level and age, Gleason score, and staging.

conclusionsOur study demonstrates that GSTP1 methylation is associated with the presence of PCa and PSA levels. This methylation marker is a potentially useful indicator for the detection and monitoring of PCa.

Indexed as

GSTP1MethylationNeoplasmsProstate

Identifiers

PMID22468217
PMCPMC3312070

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