Evidence map›Paper›PMID 34408205›Full record

ArticleScientific reports2021

CRNDE enhances the expression of MCM5 and proliferation in acute myeloid leukemia KG-1a cells by sponging miR-136-5p.

Chen Liu, Liang Zhong, Chenlan Shen, Xuan Chu, Xu Luo, Lihua Yu, Jiao Ye, Ling Xiong, Wenran Dan, Jian Li and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 26 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

11 authors at 1 institution in 1 country.

Chen LiuCentral Laboratory of Yong-Chuan Hospital, Chongqing Medical University, Chongqing, 402160, China.
Liang ZhongKey Laboratory of Laboratory Medical Diagnostics, Ministry of Education, Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, China.
Chenlan ShenCentral Laboratory of Yong-Chuan Hospital, Chongqing Medical University, Chongqing, 402160, China.
Xuan ChuCentral Laboratory of Yong-Chuan Hospital, Chongqing Medical University, Chongqing, 402160, China.
Xu LuoCentral Laboratory of Yong-Chuan Hospital, Chongqing Medical University, Chongqing, 402160, China.
Lihua YuClinical Laboratory of Yong-Chuan Hospital, Chongqing Medical University, Chongqing, 402160, China.
Jiao YeKey Laboratory of Laboratory Medical Diagnostics, Ministry of Education, Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, China.
Ling XiongCentral Laboratory of Yong-Chuan Hospital, Chongqing Medical University, Chongqing, 402160, China.
Wenran DanCentral Laboratory of Yong-Chuan Hospital, Chongqing Medical University, Chongqing, 402160, China.
Jian LiKey Laboratory of Laboratory Medical Diagnostics, Ministry of Education, Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, China.
Beizhong LiuCentral Laboratory of Yong-Chuan Hospital, Chongqing Medical University, Chongqing, 402160, China. liubeizhong@cqmu.edu.cn.
Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The long-noncoding RNA colorectal neoplasia differentially expressed (CRNDE) gene has been considered to be crucial in tumor malignancy. Although CRNDE is highly expressed in acute myeloid leukemia (AML), its mechanism of action remains unknown. In this study, GEPIA and qRT-PCR were performed to confirm the expression of CRNDE in AML samples and cell lines, respectively. CRNDE shRNA vectors were transfected to explore the biological functions of CRNDE. The cell proliferation was assessed by the CCK8 assay, while apoptosis and cell cycle distribution were measured by flow cytometry and Western blotting. The results showed that CRNDE was overexpressed in both AML samples and cell lines. CRNDE silencing inhibited proliferation and increased apoptotic rate and cell cycle arrest of KG-1a cells. The luciferase reporter assay coupled with RIP assay revealed that CRNDE act as a ceRNA. Rescue assays demonstrated that the effects of CRNDE silencing could be reversed by miR-136-5p inhibitors. In conclusion, our results expound that the CRNDE/miR-136-5p/MCM5 axis modulates cell progression and provide a new regulatory network of CRNDE in KG-1a cells.

Indexed as

Cell ProliferationGene Expression Regulation, LeukemicCell Cycle ProteinsHEK293 CellsHL-60 CellsHumansLeukemia, Myeloid, AcuteMicroRNAsNeoplasm ProteinsRNA, Long NoncodingRNA, NeoplasmCell Cycle ProteinsCRNDE RNA, humanMCM5 protein, humanMicroRNAsMIRN136 microRNA, humanNeoplasm ProteinsRNA, Long NoncodingRNA, Neoplasm

Identifiers

PMID34408205
PMCPMC8373925
OpenAlexW3193532943

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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.