Evidence map›Paper›PMID 38510491›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2024

miR-539-5p targets BMP2 to regulate Treg activation in B-cell acute lymphoblastic leukemia through TGF-β/Smads/MAPK.

Qingkai Dai, Rui Shi, Ge Zhang, Yuefang Wang, Lei Ye, Luyun Peng, Siqi Guo, Jiajing He, Hao Yang, Yongmei Jiang

Open access · diamondAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. miR-539-5p Regulates Irritable Bowel Syndrome Pathological Processes by Targeting KDM6A.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
    Article
  3. 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 1 institution in 1 country.

Qingkai Dai *Department of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Rui Shi *Department of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Ge ZhangDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Yuefang WangDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Lei YeDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Luyun PengDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Siqi GuoDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Jiajing HeDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Hao YangDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Yongmei JiangDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Ministry of Education of the People's Republic of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (mRNAs) were believed to play an important role in cancers, and this study aimed to explore the mechanism of miRNA regulating Treg in B-cell acute lymphoblastic leukemia (B-ALL). Firstly, the differentially expressed miRNAs and target genes significantly associated with Tregs were screened out by high-throughput sequencing, and their enrichment pathways were analyzed. The binding relationship between miRNA and target genes was further verified, and the effects of miRNA on the proliferation and apoptosis of B-ALL Nalm-6 cells and Treg activation were analyzed. Results showed that differentially expressed miR-539-5p was significantly under-expressed, and its target gene BMP2 was significantly over-expressed in B-ALL, and significantly enriched in the TGF-β1 pathway. In addition, both miR-539-5p and BMP2 were significantly correlated with Treg activity in B-ALL.

Indexed as

MicroRNAsPrecursor Cell Lymphoblastic Leukemia-LymphomaBone Morphogenetic Protein 2Cell ProliferationHumansT-Lymphocytes, RegulatoryTransforming Growth Factor betaTransforming Growth Factor beta1BMP2 protein, humanBone Morphogenetic Protein 2MicroRNAsMIRN539 microRNA, humanTransforming Growth Factor betaTransforming Growth Factor beta1B-cell acute lymphoblastic leukemiaBMP2miR-539-5pTGF-βTreg

Identifiers

PMID38510491
PMCPMC10954254
OpenAlexW4391779978

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.