Evidence map›Paper›PMID 30862962›Full record

ArticlePediatric research2019

CD82 supports survival of childhood acute myeloid leukemia cells via activation of Wnt/β-catenin signaling pathway.

Hongyan Ji, Li Chen, Yuqian Xing, Shanshan Li, Jianjian Dai, Ping Zhao, Yulin Wang

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Pediatric 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
0.9field-weighted citation impact, top 28% 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, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Wnt regulation of hematopoietic stem cell development and disease.Current topics in developmental biology · 2023
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Wnt Signaling in Leukemia and Its Bone Marrow Microenvironment.International journal of molecular sciences · 2020
    Review
  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

7 authors at 4 institutions in 1 country.

Hongyan JiDepartment of Pediatrics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, China.
Li ChenDepartment of Pediatrics, Anhui Provincial Cancer Hospital, Hefei, Anhui, China.
Yuqian XingDepartment of Pediatrics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, China.
Shanshan LiNursing Department, Shandong University Second Affiliated Hospital, Jinan, Shandong, China.
Jianjian DaiDepartment of Health Oncology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, China.
Ping ZhaoDepartment of Pediatrics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, China. slyyzp123@163.com.
Yulin WangDepartment of Pediatrics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, China.
Shandong Provincial Hospital · CNShandong University · CNAnhui Provincial Hospital · CNSecond Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStem cell marker CD82 plays a vital role in the oncogenesis and progression of acute myelogenous leukemia (AML), especially in sharing properties of leukemia stem cells (LSCs). The Wnt/β-catenin pathway is required for the development of LSCs in AML. The present study aimed to validate whether CD82 supports the survival of LSCs in pediatric AML via activation of Wnt/β-catenin signaling pathway.

methodsCD82 expression and its correlation with molecules downstream of Wnt/β-catenin pathway in samples from pediatric AML patients were analyzed. Forced or downregulated expression of CD82 in AML cells was evaluated for the effects of CD82 on cell proliferation, cycle regulation, apoptosis, and adriamycin chemoresistance and to validate the underlying mechanism.

resultAberrant expression of CD82 in pediatric AML patients was found. CD82 messenger RNA expression correlated positively with downstream molecules of Wnt/β-catenin pathway in AML children. Knockdown of CD82 induced apoptosis, suppressed growth, and decreased adriamycin chemoresistance in AML cells. CD82 accelerated β-catenin nuclear location and then stimulated the expression of downstream molecules of Wnt/β-catenin pathway.

conclusionCD82 regulates the proliferation and chemotherapy resistance of AML cells via activation of the Wnt/β-catenin pathway, which suggest that the CD82 may be a potential therapeutic target in AML children.

Indexed as

Wnt Signaling Pathwaybeta CateninCell Line, TumorCell SurvivalChildHumansKangai-1 ProteinLeukemia, Myeloid, Acutebeta CateninCD82 protein, humanCTNNB1 protein, humanKangai-1 Protein

Identifiers

PMID30862962
OpenAlexW2920881827

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.