Evidence map›Paper›PMID 35572733›Full record

ArticleBioMed research international2022

circZNF91 Promotes the Malignant Phenotype of Chronic Lymphocytic Leukemia Cells by Targeting the miR-1283/WEE1 Axis.

Shaoting Li, Jing Chen, Ying Fan, Xiaoli Xu, Minjian Xiong, Yonglei Qi, Wenlin Wu, Ying Zhao

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 29% 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, 2 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Epigenetics in B-CLL.International journal of genomics · 2026
    Review
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  7. Recent Progress of CircRNAs in Hematological Malignancies.International journal of medical sciences · 2024
    Review
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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

8 authors at 2 institutions in 1 country.

Shaoting Li *Department of Pharmacy, The Fifth Hospital of Wuhan, Hubei 430050, China.
Jing Chen *Department of General Medicine, Erqiao Street Community Health Service Center Affiliate of the Fifth Hospital of Wuhan, Wuhan, Hubei 430050, China.
Ying Fan *Department of Cardiology, The Fifth Hospital of Wuhan, Wuhan, Hubei 430050, China.
Xiaoli XuDepartment of Hematology, The First People's Hospital of Foshan, Foshan, Guangdong 528000, China.
Minjian XiongDepartment of Hematology, The First People's Hospital of Foshan, Foshan, Guangdong 528000, China.
Yonglei QiDepartment of Hematology, The First People's Hospital of Foshan, Foshan, Guangdong 528000, China.
Wenlin WuDepartment of Internal Medicine, Parrot Street Community Health Service Center Affiliate of the Fifth Hospital of Wuhan, Wuhan, Hubei 430050, China.ORCID https://orcid.org/0000-0002-5075-6733
Ying ZhaoDepartment of Hematology, The First People's Hospital of Foshan, Foshan, Guangdong 528000, China.ORCID https://orcid.org/0000-0002-3287-7400
First People's Hospital of Foshan · CNWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Circular RNAs (circRNAs) are frequently dysregulated in cancers and are implicated in tumorigenesis and tumor progression. In this study, we investigated the role of circZNF91 in regulating the malignant phenotype of chronic lymphocytic leukemia (CLL) cells and the underlying molecular mechanism. Material: /. Methods: The expression of circZNF91 was determined by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The binding sequences between circZNF91/miR-1283 and miR-1283/WEE1 were predicted by the bioinformatic database. The functional interactions were confirmed by the dual-luciferase reporter, RT-qPCR, and Western blot assays. The functional roles of the circZNF91/miR-1283/WEE1 axis in CLL progression were examined by cell proliferation, apoptosis, and EdU incorporation assays. Results: circZNF91 was upregulated in CLL samples. Silencing circZNF91 attenuated CLL cell proliferation and induced apoptosis and cell cycle arrest. circZNF91 could sponge miR-1283 to suppress its activity, which in turn upregulated WEE1 expression. Silencing circ-TTBK2 reduced WEE1 expression, while the inhibitor of miR-1283 enhanced WEE1 expression. The miR-1283/WEE1 axis mediated the effects of circZNF91 on cell proliferation and apoptosis, as well as induced cell cycle regulation. Conclusions: The circZNF91/miR-1283/WEE1 axis is engaged in the pathological phenotypes of CLL cells, which could serve as potential targets for future therapy development.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellMicroRNAsApoptosisCell Cycle ProteinsCell Line, TumorCell ProliferationHumansPhenotypeProtein-Tyrosine KinasesRNA, CircularCell Cycle ProteinsMicroRNAsMIRN1283 microRNA, humanProtein-Tyrosine KinasesRNA, CircularWEE1 protein, human

Identifiers

PMID35572733
PMCPMC9098290
OpenAlexW4229021925

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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.