Evidence map›Paper›PMID 27516205›Full record

ArticleJournal of hematology & oncology2016

MiR-124-3p/B4GALT1 axis plays an important role in SOCS3-regulated growth and chemo-sensitivity of CML.

Yu-Xiao Liu, Li Wang, Wen-Jia Liu, Hai-Tao Zhang, Jing-Hui Xue, Zhi-Wen Zhang, Chun-Ji Gao

Open access · goldAbstract read
In one paragraph

Article in Journal of hematology & oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

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  9. DF-MDA: An effective diffusion-based computational model for predicting miRNA-disease association.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
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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 2 institutions in 1 country.

Yu-Xiao LiuDepartment of Neurosurgery, The First Affiliated Hospital of Chinese PLA General Hospital, 51 Fushi Road, Beijing, 100048, People's Republic of China.
Li WangDepartment of Hematology, Chinese PLA General Hospital, Laoshan Branch, No. 401, Qingdao, 266100, People's Republic of China.
Wen-Jia LiuGenetic Laboratory of Development and Diseases, Beijing Institute of Biotechnology, Beijing, 100071, People's Republic of China.
Hai-Tao ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Chinese PLA General Hospital, 51 Fushi Road, Beijing, 100048, People's Republic of China.
Jing-Hui XueDepartment of Neurosurgery, The First Affiliated Hospital of Chinese PLA General Hospital, 51 Fushi Road, Beijing, 100048, People's Republic of China. xuejh629@163.com.
Zhi-Wen ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Chinese PLA General Hospital, 51 Fushi Road, Beijing, 100048, People's Republic of China.
Chun-Ji GaoDepartment of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, People's Republic of China. gaochunji@hotmail.com.
First Affiliated Hospital of Chinese PLA General Hospital · CNChinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAbnormal expression of SOCS3 has been implicated in myeloproliferative neoplasms, but the role of SOCS3 in the pathogenesis of leukemia remains largely unknown. Here, we examined the function of SOCS3 in the growth and chemo-sensitivity of chronic myeloid leukemia (CML) and explored the involved mechanisms.

methodsExpression levels of SOCS3 in several leukemia cell lines and bone marrow mononuclear cells (BMNCs) from CML patients were determined using quantitative real-time PCR (qPCR) and Western blotting (WB). The roles of SOCS3 in the proliferation, apoptosis, and drug resistance of CML cells were examined by clonogenic progenitor cell assay, flow cytometry, and CCK-8 assay. A detailed analysis of the underlying mechanism of SOCS3 in K562 cells was performed using the Human HT-12 v4 Expression BeadChip, which has more than 48000 gene probes including 600 microRNAs (miRNA) probes. The correlation between the mRNA expression of SOCS3 and miR-124-3p in BMNCs from 30 CML patients was tested by qPCR and analyzed by Pearson correlation and linear regression analysis. The potential target of miR-124-3p in CML cells was explored using the luciferase reporter assay, qPCR, and WB. The effect of SOCS3 on the miR-124-3p/B4GALT1 axis was investigated by qPCR, WB, CCK-8 assay, and tumorigenicity assays in nude mice.

resultsSOCS3 was down-regulated in CML cell lines and most of BMNCs from CML patients, and the expression level of SOCS3 was associated with the inhibition of cell proliferation and drug resistance of CML cells. Over-expression of SOCS3 in K562 cells inhibited the expression of leukemia-specific genes and promoted the expression of some miRNAs, among which miR-124-3p was the highest. SOCS3 over-expression enhanced the expression of miR-124-3p and vice versa. The mRNA expression of miR-124-3p and SOCS3 in BMNCs from 30 CML patients was positively correlated. Consistently, the tumor suppressing effects of SOCS3 were partially neutralized by the miR-124-3p inhibitor. B4GALT1 was downstream of miR-124-3p and regulated by SOCS3/miR-124-3p in vitro. Furthermore, SOCS3 over-expression could inhibit the growth and B4GALT expression of K562 cells in vivo.

conclusionsSOCS3/miR-124-3p/B4GALT1 axis plays an important role in the pathogenesis of CML.

Indexed as

AnimalsBone Marrow CellsCell Line, TumorCell ProliferationCells, CulturedDrug Resistance, NeoplasmGalactosyltransferasesGene Expression Regulation, LeukemicHumansK562 CellsLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLeukocytes, MononuclearMice, NudeMicroRNAsRNA, MessengerSuppressor of Cytokine Signaling 3 Proteinbeta-1,4-galactosyltransferase IGalactosyltransferasesMicroRNAsMIRN124 microRNA, humanRNA, MessengerSOCS3 protein, humanSuppressor of Cytokine Signaling 3 ProteinB4GALT1Chemo-sensitivityLeukemogenesismiR-124SOCS3

Identifiers

PMID27516205
PMCPMC4982324
OpenAlexW2512216010

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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.