Evidence map›Paper›PMID 24817955›Full record

ArticleInternational journal of clinical and experimental pathology2014

Metadherin contribute to BCR signaling in chronic lymphocytic leukemia.

Pei-Pei Li, Qing-Min Yao, Hui Zhou, Li-Li Feng, Xue-Ling Ge, Xiao Lv, Na Chen, Kang Lu, Xin Wang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Targeting Btk with ibrutinib inhibit gastric carcinoma cells growth.American journal of translational research · 2016
    Article
  5. 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

9 authors at 1 institution in 1 country.

Pei-Pei LiDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University Jinan, Shandong, 250012, China.
Qing-Min YaoDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University Jinan, Shandong, 250012, China.
Hui ZhouDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University Jinan, Shandong, 250012, China.
Li-Li FengDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University Jinan, Shandong, 250012, China.
Xue-Ling GeDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University Jinan, Shandong, 250012, China.
Xiao LvDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University Jinan, Shandong, 250012, China.
Na ChenDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University Jinan, Shandong, 250012, China.
Kang LuDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University Jinan, Shandong, 250012, China.
Xin WangDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University Jinan, Shandong, 250012, China ; Institute of Diagnostics, School of Medicine, Shandong University Jinan, Shandong, 250012, China.
Shandong Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have reported Metadherin (MTDH) was proven to be overexpression and involved in malignance of chronic lymphocytic leukemia (CLL) via Wnt signaling pathway. In this study, we further investigate the role of MTDH in regulation of BCR signaling pathway in CLL. Six CLL samples whose cells were proliferation after BCR activation were chosen from patients with unmutated IgVH. CCK-8 method used to evaluate the proliferation rate. MTDH expression was measured by quantitative PCR and Western blot. After BCR activation, there exist upregulation of MTDH expression in mRNA and protein level in all six CLL patients (P<0.05). In cell line MEC-1, we observed the same pro-proliferation effect accompanying with elevated MTDH expression. The proliferation effects of BCR activation to MEC-1 can be inhibited by MTDH interference. The results of this study indicate that MTDH involved in the pro-proliferation effect of BCR activation in CLL. And the results imply that MTDH can be a potential therapy target of CLL.

Indexed as

Biomarkers, TumorCell Adhesion MoleculesCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansLeukemia, Lymphocytic, Chronic, B-CellMembrane ProteinsProto-Oncogene Proteins c-bcrRNA-Binding ProteinsSignal TransductionUp-RegulationBCR protein, humanBiomarkers, TumorCell Adhesion MoleculesMembrane ProteinsMTDH protein, humanProto-Oncogene Proteins c-bcrRNA-Binding ProteinsB cell receptorChronic lymphocytic leukemiaMetadherin

Identifiers

PMID24817955
PMCPMC4014239
OpenAlexW322585581

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.