Evidence map›Paper›PMID 31902747›Full record

ArticleMolecular therapy. Nucleic acids2020

Silencing Long Non-coding RNA LINC01224 Inhibits Hepatocellular Carcinoma Progression via MicroRNA-330-5p-Induced Inhibition of CHEK1.

Dan Gong, Peng-Cheng Feng, Xing-Fei Ke, Hui-Lan Kuang, Li-Li Pan, Qiang Ye, Jian-Bing Wu

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Molecular therapy. Nucleic acids, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.9field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 71 citations in OpenAlex.

  1. Review
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  8. Bioinformatic-based mechanism identification ofJournal of gastrointestinal oncology · 2022
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  9. Translational cancer research · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Dan GongDepartment of Oncology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, P.R. China; Jiangxi Key Laboratory of Cinical and Translational Cancer Research, Nanchang 330006, P.R. China.
Peng-Cheng FengDepartment of Oncology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, P.R. China; Jiangxi Key Laboratory of Cinical and Translational Cancer Research, Nanchang 330006, P.R. China.
Xing-Fei KeDepartment of Oncology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, P.R. China; Jiangxi Key Laboratory of Cinical and Translational Cancer Research, Nanchang 330006, P.R. China.
Hui-Lan KuangDepartment of Oncology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, P.R. China; Jiangxi Key Laboratory of Cinical and Translational Cancer Research, Nanchang 330006, P.R. China.
Li-Li PanDepartment of Oncology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, P.R. China; Jiangxi Key Laboratory of Cinical and Translational Cancer Research, Nanchang 330006, P.R. China.
Qiang YeDepartment of Oncology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, P.R. China; Jiangxi Key Laboratory of Cinical and Translational Cancer Research, Nanchang 330006, P.R. China.
Jian-Bing WuDepartment of Oncology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, P.R. China; Jiangxi Key Laboratory of Cinical and Translational Cancer Research, Nanchang 330006, P.R. China. Electronic address: wujianbing_wjb@163.com.
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) accounts for approximately 85%-90% of primary liver cancers. Based on in silico analysis, differentially expressed long non-coding RNA (lncRNA) LINC01224 in HCC, the downstream microRNA (miRNA) miR-330-5p, and its target gene checkpoint kinase 1 (CHEK1) were selected as research subjects. Herein, this study was designed to evaluate their interaction effects on the malignant phenotypes of HCC cells. LINC01224 and CHEK1 were upregulated and miR-330-5p was downregulated in HCC cells. miR-330-5p shared negative correlations with LINC01224 and CHEK1, and LINC01224 shared a positive correlation with CHEK1. Notably, LINC01224 could specifically bind to miR-330-5p, and CHEK1 was identified as a target gene of miR-330-5p. When LINC01224 was silenced or miR-330-5p was elevated, the sphere and colony formation abilities and proliferative, migrative, and invasive potentials of HCC cells were diminished, while cell cycle arrest and apoptosis were enhanced. Moreover, LINC01224 induced HCC progression in vitro and accelerated tumor formation in nude mice by increasing CHEK1 expression. The key findings of the present study demonstrated that silencing LINC01224 could downregulate the expression of CHEK1 by competitively binding to miR-330-5p, thus inhibiting HCC progression. This result highlights the LINC01224/miR-330-5p/CHEK1 axis as a novel molecular mechanism involved in the pathology of HCC.

Indexed as

cancer stem cellsCHEK1 genehepatocellular carcinomalong non-coding RNA LINC01224microRNA-330-5p

Identifiers

PMID31902747
PMCPMC6948252
OpenAlexW2980506508

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.