Evidence map›Paper›PMID 26203261›Full record

ArticleOncoTargets and therapy2015

The prognostic significance of protein tyrosine phosphatase 4A2 in breast cancer.

Duanzheng Zhao, Libin Guo, Henrique Neves, Hiu-Fung Yuen, Shu-Dong Zhang, Cian M McCrudden, Qing Wen, Jin Zhang, Qi Zeng, Hang Fai Kwok and 1 more

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2015. 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
0.9field-weighted citation impact, top 26% 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, 17 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 2 institutions in 2 countries.

Duanzheng ZhaoCollege of Continuing Education, Nanjing University of Aeronautics and Astronautics, Nanjing, Jiangsu, People's Republic of China.
Libin GuoCollege of Life Sciences, Fujian Normal University, Fuzhou, Fujian, People's Republic of China.
Henrique NevesFaculty of Health Sciences, University of Macau, Avenida de Universidade, Taipa, Macau Special Administrative Region, People's Republic of China.
Hiu-Fung YuenInstitute of Molecular and Cell Biology, Biopolis Drive, Proteos, Singapore.
Shu-Dong ZhangCenter for Cancer Research and Cell Biology, Queen's University of Belfast, Belfast, UK.
Cian M McCruddenSchool of Pharmacy, Queen's University of Belfast, Belfast, UK.
Qing WenCenter for Cancer Research and Cell Biology, Queen's University of Belfast, Belfast, UK.
Jin ZhangCollege of Life Sciences, Fujian Normal University, Fuzhou, Fujian, People's Republic of China.
Qi ZengInstitute of Molecular and Cell Biology, Biopolis Drive, Proteos, Singapore.
Hang Fai KwokFaculty of Health Sciences, University of Macau, Avenida de Universidade, Taipa, Macau Special Administrative Region, People's Republic of China ; Center for Cancer Research and Cell Biology, Queen's University of Belfast, Belfast, UK ; School of Pharmacy, Queen's University of Belfast, Belfast, UK.
Yao LinCollege of Life Sciences, Fujian Normal University, Fuzhou, Fujian, People's Republic of China.
Queen's University Belfast · GBFujian Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although PTP4A3 has been shown to be a very important factor in promoting cancer progression, the role of its close family member PTP4A2 is still largely unknown. Recent reports have shown contradicting results on the role of PTP4A2 in breast cancer progression. Considering this, we aimed to investigate the prognostic value of PTP4A2 in five independent breast cancer data sets (minimum 198 patients per cohort, totaling 1,124 patients) in the Gene Expression Omnibus Database. We found that high expression of PTP4A2 was a favorable prognostic marker in all five independent breast cancer data sets, as well as in the combined cohort, with a hazard ratio of 0.68 (95% confidence interval =0.56-0.83; P<0.001). Low PTP4A2 expression was associated with estrogen receptor-negative tumors and tumors with higher histological grading; furthermore, low expression was inversely correlated with the expression of genes involved in proliferation, including MKI67 and the MCM gene family encoding the minichromosome maintenance proteins. These findings suggest that PTP4A2 may play a role in breast cancer progression by dysregulating cell proliferation. PTP4A2 expression was positively correlated with ESR1, the gene encoding estrogen receptor-alpha, and inversely correlated with EGFR expression, suggesting that PTP4A2 may be involved in these two important oncogenic pathways. Together, our results suggest that expression of PTP4A2 is a favorable prognostic marker in breast cancer.

Indexed as

breast cancerminichromosome maintenance proteinsoverexpressionprognostic markerPTP4A2survival

Identifiers

PMID26203261
PMCPMC4508076
OpenAlexW1862488265

What OpenQuestion holds

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LicenceCC BY-NC
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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.