Evidence map›Paper›PMID 21872824›Full record

ArticleCancer genetics2011

Evaluation of PPP2R2A as a prostate cancer susceptibility gene: a comprehensive germline and somatic study.

Yu Cheng, Wennuan Liu, Seong-Tae Kim, Jishan Sun, Lingyi Lu, Jielin Sun, Siqun Lilly Zheng, William B Isaacs, Jianfeng Xu

Abstract read
In one paragraph

Article in Cancer genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

47 citing papers in PubMed, 62 citations in OpenAlex.

  1. Trial
  2. Article
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  4. Article
  5. Targeting PP2A in cancer: an underrated option.Journal of experimental & clinical cancer research : CR · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. LowTheranostics · 2024
    Article
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  18. Article
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  20. Molecular crosstalk between cancer and neurodegenerative diseases.Cellular and molecular life sciences : CMLS · 2020
    Review
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 2 institutions in 1 country.

Yu ChengCenter for Cancer Genomics, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Wennuan Liu
Seong-Tae Kim
Jishan Sun
Lingyi Lu
Jielin Sun
Siqun Lilly Zheng
William B Isaacs
Jianfeng Xu
Wake Forest University · USJohns Hopkins University · US

Funding

Mapping Prostate Cancer Susceptibility Genes at 8p22-23R01CA095052 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI XU, JIANFENG · 2003 to 2007
$1.4M
NCI NIH HHS CA95052NCI NIH HHS R01 CA095052
6 · The paper itself

Abstract

PPP2R2A, mapped to 8p21.2, codes for the α isoform of the regulatory B55 subfamily of protein phosphatase 2 (PP2A). PP2A is one of the four major serine/threonine phosphatases and is implicated in the negative control of cell growth and division. Because of its known functions and location within a chromosomal region where evidence for linkage and somatic loss of heterozygosity was found, we hypothesized that either somatic copy number changes or germline sequence variants in PPP2R2A may increase prostate cancer (PCa) risk. We examined PPP2R2A deletion status in 141 PCa samples using Affymetrix SNP arrays. It was found that PPP2R2A was commonly (67.1%) deleted in tumor samples, including a homozygous deletion in three tumors (2.1%). We performed a mutation screen for PPP2R2A in 96 probands of hereditary prostate cancer families. No high risk mutations were identified. In addition, we re-analyzed 10 SNPs of PPP2R2A in sporadic PCa cases and controls. No significant differences in the allele and genotype frequencies were observed among either PCa cases and controls or PCa aggressive and non-aggressive cases. Taken together, these results suggest that a somatic deletion rather than germline sequence variants of PPP2R2A may play a more important role in PCa susceptibility.

Indexed as

Genetic Predisposition to Disease3' Untranslated Regions5' Untranslated RegionsAllelesDNA Copy Number VariationsDNA Mutational AnalysisDNA, NeoplasmExonsGene DeletionGene FrequencyGenetic LinkageGerm-Line MutationHumansMaleMiddle AgedPolymorphism, Single Nucleotide3' Untranslated Regions5' Untranslated RegionsDNA, NeoplasmPPP2R2A protein, humanProtein Phosphatase 2

Identifiers

PMID21872824
PMCPMC3722858
OpenAlexW2164348209

What OpenQuestion holds

Textmetadata
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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.