Evidence map›Paper›PMID 26884884›Full record

ArticleInternational journal of clinical and experimental pathology2015

High expression of dual-specificity phosphatase 5 pseudogene 1 (DUSP5P1) is associated with poor prognosis in acute myeloid leukemia.

Ling-Yu Zhou, Jia-Yu Yin, Qin Tang, Ling-Ling Zhai, Tin-Juan Zhang, Yu-Xin Wang, Dong-Qin Yang, Jun Qian, Jiang Lin, Zhao-Qun Deng

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Trial
  2. Pseudogenes in the carcinogenesis: epithelial-to-mesenchymal transition process and cancer initiating cells.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Pseudogenes as Biomarkers and Therapeutic Targets in Human Cancers.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  8. Low Expression of Pseudogene POU5F1B Affects Diagnosis and Prognosis in Acute Myeloid Leukemia (AML).Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  9. 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

10 authors.

Ling-Yu ZhouDepartment of Hematology, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China; Department of Laboratory Center, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China.
Jia-Yu YinDepartment of Hematology, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China; Department of Laboratory Center, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China.
Qin TangDepartment of Laboratory Center, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China; Department of Hematology, The Affiliated Jintan Hospital of Jiangsu UniversityPeople's Republic of China.
Ling-Ling ZhaiDepartment of Hematology, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China; Department of Laboratory Center, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China.
Tin-Juan ZhangDepartment of Hematology, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China; Department of Laboratory Center, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China.
Yu-Xin WangDepartment of Hematology, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China; Department of Laboratory Center, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China.
Dong-Qin YangDepartment of Hematology, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China; Department of Laboratory Center, The Affiliated People's Hospital of Jiangsu UniversityZhenjiang 212002, Jiangsu, People's Republic of China.
Jun QianDepartment of Hematology, The Affiliated People's Hospital of Jiangsu University Zhenjiang 212002, Jiangsu, People's Republic of China.
Jiang LinDepartment of Laboratory Center, The Affiliated People's Hospital of Jiangsu University Zhenjiang 212002, Jiangsu, People's Republic of China.
Zhao-Qun DengDepartment of Laboratory Center, The Affiliated People's Hospital of Jiangsu University Zhenjiang 212002, Jiangsu, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study was to investigate the expression status of Dual-Specificity Phosphatase 5 Pseudogene 1 (DUSP5P1) and its clinical relevance in patients with acute myeloid leukemia (AML). Real-time quantitative PCR (RQ-PCR) was performed to detect the status of DUSP5P1 expression in 89 patients with de novo AML and 24 normal controls. The level of DUSP5P1 expression was significantly up-regulated in AML compared to controls (P=0.031). The patients with high expression of DUSP5P1 had higher percentage of blasts in bone marrow (BM) than those without high expression (P=0.027). The occurrence rate of DUSP5P1 high expression was significantly higher in M1 (2/8, 25%) and M2 subtypes (9/33, 27%) than in M3 subtype (0/17, 0%) (P=0.034). At the same time, the frequency of DUSP5P1 high expression in patients with intermediate (13/53, 24%) and poor karyotypes (5/11, 45%) was significantly higher than that in patients with favorable karyotype (0/21, 0%) (P=0.003). Meanwhile, DUSP5P1 high-expressed patients had significantly shorter overall survival (OS) than those with low expression (median 4.5 vs. 10.5 months, respectively, P=0.038). Our findings indicated that high expression of DUSP5P1 may identify high-risk AML patients and is associated with poor prognosis in AML.

Indexed as

AdolescentAdultAgedAged, 80 and overBiomarkers, TumorCase-Control StudiesChildFemaleHumansKaplan-Meier EstimateKaryotypeLeukemia, Myeloid, AcuteMaleMiddle AgedPrognosisPseudogenesBiomarkers, Tumoracute myeloid leukemia (AML)DUSP5P1prognosticPseudogene

Identifiers

PMID26884884
PMCPMC4730097

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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.