Evidence map›Paper›PMID 30883341›Full record

ArticleCancer biomarkers : section A of Disease markers2019

MiR-19b and miR-20a suppress apoptosis, promote proliferation and induce tumorigenicity of multiple myeloma cells by targeting PTEN.

Jie Yuan, Zhangyao Su, Wenchao Gu, Xianjuan Shen, Qiumin Zhao, Linying Shi, Chunjing Jin, Xudong Wang, Hui Cong, Shaoqing Ju

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
2.9field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Multiple Myeloma: Genetic and Epigenetic Biomarkers with Clinical Potential.International journal of molecular sciences · 2024
    Article
  6. Article
  7. Dysregulated transfer RNA-derived small RNAs as potential gastric cancer biomarkers.Experimental biology and medicine (Maywood, N.J.) · 2024
    Article
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  11. Review
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  20. Expression of miRNA-25 in young and old lung adenocarcinoma.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2021
    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

10 authors at 2 institutions in 1 country.

Jie YuanDepartment of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Zhangyao SuNantong University, Nantong, Jiangsu, China.
Wenchao GuDepartment of Rheumatology, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Xianjuan ShenResearch Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Qiumin ZhaoNantong University, Nantong, Jiangsu, China.
Linying ShiNantong University, Nantong, Jiangsu, China.
Chunjing JinDepartment of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Xudong WangDepartment of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Hui CongDepartment of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Shaoqing JuDepartment of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Nantong University · CNAffiliated Hospital of Nantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a common hematological malignancy that is often associated with osteolytic lesions, anemia and renal impairment. Deregulation of miRNA has been implicated in the pathogenesis of MM. It was found in our study that miR-19b and miR-20a as members of crucial oncogene miR-17-92 cluster were differentially expressed between patients with MM and normal controls by genechip microarray, and this result was further confirmed in sera of patients with MM by qRT-PCR. The functional effect of miR-19b/20a was analyzed and results showed that miR-19b/20a promoted cell proliferation and migration, inhibited cell apoptosis and altered cell cycle in MM cells. PTEN protein expression was reduced after transfection of miR-19b/20a, suggesting that PTEN was a direct target of miR-19b/20a. In addition, over-expression of miR-19b/20a reversed the anti-proliferation and pro-apoptosis effect of PTEN in MM cells. Finally, our in vivo experiment demonstrated that lentivirus-mediated delivery of miR-20a promoted tumor growth in murine xenograft model of MM, which provide evidence that miR-20a inhibitor exerts therapeutic activity in preclinical models and supports a framework for the development of miR-19b/20a-based treatment strategies for MM patients.

Indexed as

AgedAged, 80 and overAnimalsApoptosisBiomarkers, TumorCase-Control StudiesCell CycleCell Line, TumorCell MovementCell ProliferationCell Transformation, NeoplasticComputational BiologyDisease Models, AnimalFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticBiomarkers, TumorMicroRNAsMIRN19A microRNA, humanMIRN20a microRNA, humanPTEN PhosphohydrolasePTEN protein, humanmiR-19bmiR-20aMultiple myelomaPTEN

Identifiers

PMID30883341
PMCPMC13082517
OpenAlexW2920925845

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.