Evidence map›Paper›PMID 34587164›Full record

ArticlePloS one2021

MiR-20a-5p functions as a potent tumor suppressor by targeting PPP6C in acute myeloid leukemia.

Fengchang Bao, Lei Zhang, Xiaohang Pei, Cheng Lian, Yanhui Liu, Hongna Tan, Pingchong Lei

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 34% 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, 1 synthesis or guideline pooled it, 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

7 authors at 1 institution in 1 country.

Fengchang BaoDepartment of Hematology, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Lei ZhangBlood institute, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Xiaohang PeiDepartment of Hematology, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Cheng LianDepartment of Hematology, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Yanhui LiuDepartment of Hematology, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Hongna TanMedical Imaging Center, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Pingchong LeiDepartment of Hematology, Henan Provincial People's Hospital, Zhengzhou, Henan, China.ORCID 0000-0002-7148-1652
Henan Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is as a highly aggressive and heterogeneous hematological malignancy. MiR-20a-5p has been reported to function as an oncogene or tumor suppressor in several tumors, but the clinical significance and regulatory mechanisms of miR-20a-5p in AML cells have not been fully understood. In this study, we found miR-20a-5p was significantly decreased in bone marrow from AML patients, compared with that in healthy controls. Moreover, decreased miR-20a-5p expression was correlated with risk status and poor survival prognosis in AML patients. Overexpression of miR-20a-5p suppressed cell proliferation, induced cell cycle G0/G1 phase arrest and apoptosis in two AML cell lines (THP-1 and U937) using CCK-8 assay and flow cytometry analysis. Moreover, miR-20a-5p overexpression attenuated tumor growth in vivo by performing tumor xenograft experiments. Luciferase reporter assay and western blot demonstrated that protein phosphatase 6 catalytic subunit (PPP6C) as a target gene of miR-20a-5p was negatively regulated by miR-20a-5p in AML cells. Furthermore, PPP6C knockdown imitated, while overexpression reversed the effects of miR-20a-5p overexpression on AML cell proliferation, cell cycle G1/S transition and apoptosis. Taken together, our findings demonstrate that miR-20a-5p/PPP6C represent a new therapeutic target for AML and a potential diagnostic marker for AML therapy.

Indexed as

Gene Expression Regulation, LeukemicAdultAnimalsApoptosisBase SequenceBone MarrowCase-Control StudiesCell Cycle CheckpointsCell Line, TumorCell ProliferationFemaleHumansLeukemia, Myeloid, AcuteMaleMiceMice, KnockoutMicroRNAsMIRN20a microRNA, humanPhosphoprotein Phosphatasesprotein phosphatase 6

Identifiers

PMID34587164
PMCPMC8480815
OpenAlexW3202283796

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.