Evidence map›Paper›PMID 32655783›Full record

ArticleAmerican journal of translational research2020

LncRNA LINC00265/miR-485-5p/IRF2-mediated autophagy suppresses apoptosis in acute myeloid leukemia cells.

Feng Zhang, Qianwen Li, Kai Zhu, Junfeng Zhu, Jiajia Li, Yuan Yuan, Pingping Zhang, Lili Zhou, Lin Liu

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed, 27 citations in OpenAlex.

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  8. Silencing of the long non-coding RNAOncology research · 2024
    Article
  9. Review
  10. The dual role of autophagy in acute myeloid leukemia.Journal of hematology & oncology · 2022
    Review
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  12. Article
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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 1 institution in 1 country.

Feng ZhangDepartment of Hematology, The First Affiliated Hospital of Bengbu Medical College Bengbu 233004, Anhui, PR China.
Qianwen LiDepartment of Hematology, The First Affiliated Hospital of Bengbu Medical College Bengbu 233004, Anhui, PR China.
Kai ZhuDepartment of Hematology, The First Affiliated Hospital of Bengbu Medical College Bengbu 233004, Anhui, PR China.
Junfeng ZhuDepartment of Hematology, The First Affiliated Hospital of Bengbu Medical College Bengbu 233004, Anhui, PR China.
Jiajia LiDepartment of Hematology, The First Affiliated Hospital of Bengbu Medical College Bengbu 233004, Anhui, PR China.
Yuan YuanDepartment of Hematology, The First Affiliated Hospital of Bengbu Medical College Bengbu 233004, Anhui, PR China.
Pingping ZhangDepartment of Hematology, The First Affiliated Hospital of Bengbu Medical College Bengbu 233004, Anhui, PR China.
Lili ZhouDepartment of Hematology Laboratory, The First Affiliated Hospital of Bengbu Medical College Bengbu 233004, Anhui, PR China.
Lin LiuDepartment of Hematology, The First Affiliated Hospital of Bengbu Medical College Bengbu 233004, Anhui, PR China.
First Affiliated Hospital of Bengbu Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExtensive studies have shown that long non-coding RNAs (lncRNAs) play important roles in multiple cancers. The present study aimed to investigate the role and mechanism of lncRNA LINC00265 in the regulation of apoptosis in acute myeloid leukemia (AML) cells.

methodsGain- or loss-of-function experiments were conducted in AML cells to explore the effect of LINC00265 on AML. Autophagy was assessed by examining levels of Beclin-1, p62, and ratio of LC3-II/LC3-I. Cell proliferation and apoptosis of AML cells were evaluated by CCK-8 assay and flow cytometry, respectively. RNA pull-down was performed to enrich miR-485-5p interacted with LINC00265. The interaction between miR-485-5p and IRF2 3'UTR was analyzed by luciferase reporter assay.

resultsLINC00265 expression was significantly up-regulated, whereas miR-485-5p was down-regulated in serum of AML patients and AML cell lines. LINC00265 promoted, whereas miR-485-5p suppressed autophagy in AML cells. Mechanistically, LINC00265 functioned as a ceRNA for miR-485-5p to facilitate IRF2 expression. More importantly, LINC00265 overexpression or miR-485-5p inhibitor reversed the 3-methyladenine (3-MA, an autophagy inhibitor)-mediated proliferation-inhibitory and pro-apoptotic effects, whereas LINC00265 silencing or miR-485-5p mimic overturned the proliferation-promoting and anti-apoptotic effects of autophagy activator rapamycin.

conclusionLINC00265 attenuates AML cell apoptosis by inducing autophagy via miR-485/IRF2 axis.

Indexed as

acute myeloid leukemiaapoptosisautophagyLINC00265

Identifiers

PMID32655783
PMCPMC7344095
OpenAlexW3042549089

What OpenQuestion holds

Textmetadata
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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.