Evidence map›Paper›PMID 30578412›Full record

ArticleCancer gene therapy2020

Overexpression of PDK2 and PDK3 reflects poor prognosis in acute myeloid leukemia.

Longzhen Cui, Zhiheng Cheng, Yan Liu, Yifeng Dai, Yifan Pang, Yang Jiao, Xiaoyan Ke, Wei Cui, Qingyi Zhang, Jinlong Shi and 1 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 51 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 9 institutions in 3 countries.

Longzhen Cui *Translational Medicine Center, Huaihe Hospital of Henan University, Kaifeng, 475000, China.
Zhiheng Cheng *Translational Medicine Center, Huaihe Hospital of Henan University, Kaifeng, 475000, China.
Yan LiuTranslational Medicine Center, Huaihe Hospital of Henan University, Kaifeng, 475000, China.
Yifeng DaiLaboratory of Environmental Medicine and Developmental Toxicology, Shantou University Medical College, Shantou, 515041, China.
Yifan PangDepartment of Medicine, William Beaumont Hospital, Royal Oak, MI, 48073, USA.
Yang JiaoLife Sciences Institute and Innovation Center for Cell Signaling Network, Zhejiang University, Hangzhou, 310058, China.ORCID http://orcid.org/0000-0002-1077-6422
Xiaoyan KeDepartment of Hematology and Lymphoma Research Center, Peking University, Third Hospital, Beijing, 100191, China.
Wei Cui *Department of Clinical Laboratory, Beijing Haidian Hospital, Beijing Haidian Section of Peking University Third Hospital, Beijing, 100080, China.
Qingyi Zhang *Department of Hematology of Air Force PLA General Hospital, Beijing, China.
Jinlong Shi *Translational Medicine Center, Huaihe Hospital of Henan University, Kaifeng, 475000, China.
Lin Fu *Translational Medicine Center, Huaihe Hospital of Henan University, Kaifeng, 475000, China. fulin022@126.com.ORCID http://orcid.org/0000-0002-2416-7572
Peking University · CNAir Force General Hospital PLA · CNBeaumont Hospital, Royal Oak · USBeijing Haidian Hospital · CNChinese PLA General Hospital · CNHenan University Huaihe Hospital and Huaihe Clinical Institute · CNShantou University · CNUniversity Medical Center Groningen · NLZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a hematological malignancy characterized by the proliferation of immature myeloid cells, with impaired differentiation and maturation. Pyruvate dehydrogenase kinase (PDK) is a pyruvate dehydrogenase complex (PDC) phosphatase inhibitor that enhances cell glycolysis and facilitates tumor cell proliferation. Inhibition of its activity can induce apoptosis of tumor cells. Currently, little is known about the role of PDKs in AML. Therefore, we screened The Cancer Genome Atlas (TCGA) database for de novo AML patients with complete clinical information and PDK family expression data, and 84 patients were included for the study. These patients did not undergo allogeneic hematopoietic stem cell transplantation (allo-HSCT). Univariate analysis showed that high expression of PDK2 was associated with shorter EFS (P = 0.047), and high expression of PDK3 was associated with shorter OS (P = 0.026). In multivariate analysis, high expression of PDK3 was an independent risk factor for EFS and OS (P < 0.05). In another TCGA cohort of AML patients who underwent allo-HSCT (n = 71), PDK expression was not associated with OS (all P > 0.05). Our results indicated that high expressions of PDK2 and PDK3, especially the latter, were poor prognostic factors of AML, and the effect could be overcome by allo-HSCT.

Indexed as

Hematopoietic Stem Cell TransplantationAdultAgedAged, 80 and overBiomarkers, TumorBone MarrowDatasets as TopicDisease-Free SurvivalFemaleGene Expression Regulation, LeukemicHumansKaplan-Meier EstimateLeukemia, Myeloid, AcuteMaleMiddle AgedPrognosisBiomarkers, TumorPDK2 protein, humanPDK3 protein, humanPyruvate Dehydrogenase Acetyl-Transferring Kinase

Identifiers

PMID30578412
OpenAlexW2905857451

What OpenQuestion holds

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Registered trials

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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.