Evidence map›Paper›PMID 32249364›Full record

ArticleCytotechnology2020

NOL6, a new founding oncogene in human prostate cancer and targeted by miR-590-3p.

Degang Dong, Mei Song, Xiaoli Wu, Wanchun Wang

Open access · greenAbstract read
In one paragraph

Article in Cytotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 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

4 authors at 2 institutions in 1 country.

Degang DongSchool of Life Sciences, Jiangxi University of Traditional Chinese Medicine, Nanchang, 330004, People's Republic of China.
Mei SongSchool of Science and Technology, Jiangxi University of Traditional Chinese Medicine, Nanchang, 330004, People's Republic of China.
Xiaoli WuCollege of Chinese Medicine, Hunan University of Traditional Chinese Medicine, Changsha, 410208, People's Republic of China.
Wanchun WangAffiliated Hospital of Jiangxi University of Traditional Chinese Medicine, Nanchang, 330006, People's Republic of China. 1210569577@qq.com.ORCID http://orcid.org/0000-0002-2060-1773
Jiangxi University of Traditional Chinese Medicine · CNHunan University of Traditional Chinese Medicine · CN

Funding

Jiangxi Provincial Department of Science and Technology (CN) 20141BBG70052
6 · The paper itself

Abstract

We identified a new human prostate cancer oncogene, nucleolar protein 6 (NOL6), and screened for microRNAs that interfere with its expression in prostate cancer cells. A NOL6 shRNA plasmid was constructed and packaged into lentivirus to infect PC-3 cells. The ability of cell proliferation was evaluated by cell counting and colony formation. Cell cycle progression and apoptosis of PC-3 cells were detected by flow cytometry. A retrieval database was used to screen possible target microRNAs, and the effect of target miRNA overexpression on PC-3 cells was observed. The results showed that after NOL6 gene knockdown, PC-3 cell mitosis was blocked, proliferation was decreased, and the number of apoptotic cells were increased. The microRNA, hsa-miR-590-3p, that can regulate the NOL6 gene expression was identified. Overexpression of miR-590-3p in PC-3 cells by synthetic mimics resulted in abnormal mitosis, decreased cell proliferation, and an increase in apoptosis. In summary, we identified NOL6 as a novel oncogene in the human prostate cancer PC-3 cell line. The miRNA miR-590-3p interferes with NOL6 expression making it a potential treatment for prostate cancer.

Indexed as

miR-590-3pNOL6OncogeneProstate cancer

Identifiers

PMID32249364
PMCPMC7225224
OpenAlexW3014320342

What OpenQuestion holds

Textmetadata
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.