Evidence map›Paper›PMID 32338183›Full record

ArticleCancer biology & therapy2020

LINC01128 resisted acute myeloid leukemia through regulating miR-4260/NR3C2.

Haixia Li, Xuefei Tian, Paoqiu Wang, Jihong Hu, Rong Qin, Ronghua Xu, Kai Liu, Jingquan Hao, Nie Tian

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Haixia LiThe Third Department of Rehabilitation (Department of Integrated Chinese and Western Medicine), Hunan Children's Hospital , Changsha, Hunan, China.
Xuefei TianCollege of Integrated Chinese and Western Medicine, Hunan University of Chinese Medicine.
Paoqiu WangThe Third Department of Rehabilitation (Department of Integrated Chinese and Western Medicine), Hunan Children's Hospital , Changsha, Hunan, China.
Jihong HuThe First Department of Rehabilitation, Hunan Children's Hospital , Changsha, Hunan, China.
Rong QinThe Second Department of Rehabilitation, Hunan Children's Hospital , Changsha, Hunan, China.
Ronghua XuDepartment of Hematology, The First Hospital of Hunan University of Traditional Chinese Medicine , Changsha, Hunan, China.
Kai LiuDepartment of Hematology, The First Hospital of Hunan University of Traditional Chinese Medicine , Changsha, Hunan, China.
Jingquan HaoDepartment of Hematology, The First Hospital of Hunan University of Traditional Chinese Medicine , Changsha, Hunan, China.
Nie TianDepartment of Hematology, The First Hospital of Hunan University of Traditional Chinese Medicine , Changsha, Hunan, China.
First Affiliated Hospital of Hunan University of Traditional Chinese Medicine · CNHunan Children's Hospital · CNHunan University · CNHunan University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a prevalent class of blood disease with a high occurrence rate and relapse rate. The role of dysregulated microRNAs (miRNAs) in AML is emerging. MiR-4260 was identified to be a carcinogenic miRNA in colorectal cancer, but never has it been reported in AML. We aimed to study the function and mechanism of miR-4260 in AML. The miR-4260 level was higher in AML cell lines than the normal cell lines. Inhibition of miR-4260 hindered proliferation and increased apoptosis of AML cells. Mechanistically, long intergenic non-protein coding RNA 1128 (LINC01128) competed with nuclear receptor subfamily 3 group C member 2 (NR3C2) for miR-4260 so as to upregulate NR3C2. We identified the reduced levels of LINC01128 and NR3C2 in AML and it was suggested through rescue assays that LINC01128 repressed AML progression through regulating miR-4260/NR3C2 axis. In conclusion, we firstly uncovered that LINC01128 resisted acute myeloid leukemia through regulating miR-4260/NR3C2, providing novel clues for the treatment improvement of AML.

Indexed as

ApoptosisHEK293 CellsHL-60 CellsHumansLeukemia, Myeloid, AcuteReceptors, MineralocorticoidRNA, Long NoncodingTHP-1 CellsTransfectionU937 CellsUp-RegulationNR3C2 protein, humanReceptors, MineralocorticoidRNA, Long NoncodingAMLLINC01128miR-4260NR3C2

Identifiers

PMID32338183
PMCPMC7515539
OpenAlexW3018456970

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.