Evidence map›Paper›PMID 31632581›Full record

ArticleAmerican journal of translational research2019

Prognostic value of the PDLIM family in acute myeloid leukemia.

Longzhen Cui, Zhiheng Cheng, Kai Hu, Yifan Pang, Yan Liu, Tingting Qian, Liang Quan, Yifeng Dai, Ying Pang, Xu Ye and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  3. Article
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  6. Article
  7. Review
  8. Article
  9. Article
  10. PDLIM2: Signaling pathways and functions in cancer suppression and host immunity.Biochimica et biophysica acta. Reviews on cancer · 2021
    Review
  11. Article
  12. Article
  13. Article
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

12 authors at 6 institutions in 3 countries.

Longzhen CuiDepartment of Hematology, The Second Affiliated Hospital of Guangzhou Medical University Guangzhou 510260, Guangdong, China.
Zhiheng ChengDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen Groningen, Netherlands.
Kai HuDepartment of Hematology and Lymphoma Research Center, Peking University, Third Hospital Beijing 100191, China.
Yifan PangDepartment of Medicine, William Beaumont Hospital Royal Oak, MI 48073, USA.
Yan LiuTranslational Medicine Center, Huaihe Hospital of Henan University Kaifeng 475000, Henan, China.
Tingting QianDepartment of Hematology, The Second Affiliated Hospital of Guangzhou Medical University Guangzhou 510260, Guangdong, China.
Liang QuanDepartment of Hematology, The Second Affiliated Hospital of Guangzhou Medical University Guangzhou 510260, Guangdong, China.
Yifeng DaiImmunoendocrinology, Division of Medical Biology, Department of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen Groningen, Netherlands.
Ying PangDepartment of Hematology, The Second Affiliated Hospital of Guangzhou Medical University Guangzhou 510260, Guangdong, China.
Xu YeDepartment of Hematology, The Second Affiliated Hospital of Guangzhou Medical University Guangzhou 510260, Guangdong, China.
Jinlong ShiDepartment of Medical Big Data, Chinese PLA General Hospital Beijing 100853, China.
Lin FuDepartment of Hematology, The Second Affiliated Hospital of Guangzhou Medical University Guangzhou 510260, Guangdong, China.
Second Affiliated Hospital of Guangzhou Medical University · CNHenan University Huaihe Hospital and Huaihe Clinical Institute · CNUniversity Medical Center Groningen · NLBeaumont Hospital, Royal Oak · USChinese PLA General Hospital · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a genetically complex, highly aggressive hematological malignancy. Prognosis is usually with grim. PDZ and LIM domain proteins (PDLIM) are involved in the regulation of a variety of biological processes, including cytoskeletal organization, cell differentiation, organ development, neural signaling or tumorigenesis. The clinical and prognostic value of the PDLIM family in AML is unclear. To understand the role of PDLIM expression in AML, The Cancer Genome Atlas (TCGA) database was screened and 155 de novo AML patients with complete clinical information and the expression data of the PDLIM family were included in the study. The clinical and molecular characteristics associated with the expression of different members of the PDLIM family were summarized using various statistical methods. In 84 patients who only received chemotherapy, univariate analysis indicated that high expression of PDLIM2 or PDLIM7 was associated with shorter EFS and OS (both P<0.05 for PDLIM2, and both P<0.01 for PDLIM7). Multivariate analysis suggested that high expression of PDLIM7 was an independent risk factor for EFS and OS (both P<0.05). In the other 71 patients who underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT), survival was unaffected by PDLIM expressions. In summary, high expression of

Indexed as

Acute myeloid leukemiamutational spectrumnext generation sequencingPDLIMprognosis

Identifiers

PMID31632581
PMCPMC6789254
OpenAlexW2988815622

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.