Evidence map›Paper›PMID 33447422›Full record

ArticleJournal of thoracic disease2020

Low expression of long non-coding RNA ARAP1-AS1 can inhibit lung cancer proliferation by inducing G0/G1 cell cycle organization.

Xinlu Tao, Yan Zhang, Jiaping Li, Zhengzheng Ni, Zheng Tao, Qi You, Zhijie He, Dengjun Huang, Shiying Zheng

Open access · diamondAbstract read
In one paragraph

Article in Journal of thoracic disease, 2020. 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
0.6field-weighted citation impact, top 37% 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, 16 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

9 authors at 2 institutions in 1 country.

Xinlu TaoDepartment of Thoracic Surgery, The First Affiliated Hospital of Soochow University, Suzhou, China.
Yan ZhangDepartment of Thoracic Surgery, Yijishan Hospital, First Affiliated Hospital of Wannan Medical College, Wuhu, China.
Jiaping LiDepartment of Thoracic Surgery, Yijishan Hospital, First Affiliated Hospital of Wannan Medical College, Wuhu, China.
Zhengzheng NiDepartment of Thoracic Surgery, Yijishan Hospital, First Affiliated Hospital of Wannan Medical College, Wuhu, China.
Zheng TaoDepartment of Thoracic Surgery, Yijishan Hospital, First Affiliated Hospital of Wannan Medical College, Wuhu, China.
Qi YouDepartment of Thoracic Surgery, Yijishan Hospital, First Affiliated Hospital of Wannan Medical College, Wuhu, China.
Zhijie HeDepartment of Thoracic Surgery, Yijishan Hospital, First Affiliated Hospital of Wannan Medical College, Wuhu, China.
Dengjun HuangDepartment of Thoracic Surgery, Yijishan Hospital, First Affiliated Hospital of Wannan Medical College, Wuhu, China.
Shiying ZhengDepartment of Thoracic Surgery, The First Affiliated Hospital of Soochow University, Suzhou, China.
First Affiliated Hospital of Wannan Medical College · CNFirst Affiliated Hospital of Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis paper examines the expression, function, and molecular mechanism of long non-coding ribonucleic acid (lncRNA) ARAP1 antisense RNA 1 (ARAP1-AS1) in lung cancer. Specifically, it aims to clarify the molecular mechanism of lncRNA ARAP1-AS1 that affects the occurrence and development of lung cancer, and provide a theoretical basis and molecular targets for targeted therapy or early diagnosis of lung cancer.

methodsFluorescence quantitative detection of lncRNA ARAP1-AS1 expression in lung cancer tissues and cell lines, and methylthiazolyldiphenyl-tetrazolium (MTT), plate cloning experiment, and flow cytometry were used to detect the effect of knockdown of lncRNA ARAP1-AS1 on cell proliferation, clone formation, and the cell cycle, respectively. Western blotting was used to detect the expression of cell cycle-related proteins as well as the effect of knockdown of lncRNA ARAP1-AS1 on lung cancer. Cell proliferation was assessed by a nude mouse subcutaneous tumor formation experiment.

resultsLncRNA ARAP1-AS1 is highly expressed in lung cancer tissues and cells. Knockdown of LncRNA ARAP1-AS1 can significantly inhibit the proliferation and clonal formation of lung cancer cells and induce G0/G1 cell cycle arrest. Knockdown of ARAP1-AS1 can markedly inhibit the expression of cell cycle-related protein cyclin D1, but has no significant effect on the expression of cyclin-dependent kinase (CDK)4 and CDK6. Furthermore, knockdown of ARAP1-AS1 can also notably inhibit the growth of lung cancer cells and substantially reduce the expression of Ki-67 in tumor-bearing tissues in nude mice.

conclusionsLncRNA ARAP1-AS1 is highly expressed in lung cancer. Knocking down of this gene can significantly inhibit cell proliferation

Indexed as

cell proliferationcycle arrestlong non-coding ribonucleic acid ARAP1 antisense RNA 1 (lncRNA ARAP1-AS1)Lung cancernude mice

Identifiers

PMID33447422
PMCPMC7797826
OpenAlexW3115832529

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.