Evidence map›Paper›PMID 36210981›Full record

ArticleComputational intelligence and neuroscience2022

The Drosha-Independent MicroRNA6778-5p/GSK3

Mingjun Ren, Li Xing, Wanping Wang, Wanying Bi, Wanjun Wu, Gui Jiang, Weiji Wang, Xingdong Liang, Manran Liu, Shifu Tang

Open access · hybridAbstract read
In one paragraph

Article in Computational intelligence and neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 60% 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

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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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 3 institutions in 1 country.

Mingjun RenDepartment of Laboratory Medicine, Liuzhou People's Hospital, Liu Zhou 545006, China.ORCID https://orcid.org/0000-0002-4628-6900
Li XingGraduate School, Guangxi University of Chinese Medicine, Nanning 530000, China.
Wanping WangGraduate School, Guangxi University of Chinese Medicine, Nanning 530000, China.
Wanying BiGraduate School, Guangxi University of Chinese Medicine, Nanning 530000, China.
Wanjun WuDepartment of Laboratory Medicine, Liuzhou Traditional Chinese Medicine Hospital, Liu Zhou 545006, China.
Gui JiangDepartment of Laboratory Medicine, Liuzhou Traditional Chinese Medicine Hospital, Liu Zhou 545006, China.
Weiji WangGastrointestinal Surgery, Liuzhou People's Hospital, Liu Zhou 545006, China.
Xingdong LiangDepartment of Laboratory Medicine, Liuzhou People's Hospital, Liu Zhou 545006, China.
Manran LiuLaboratory Medical College, Chongqing Medical University, Chongqing 400016, China.
Shifu TangDepartment of Laboratory Medicine, Liuzhou People's Hospital, Liu Zhou 545006, China.ORCID https://orcid.org/0000-0003-1680-5041
Guangxi University · CNLiuzhou General Hospital · CNChongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gastric cancer (GC) is a primary cause of cancer death around the world. Previous studies have found that Drosha plays a significant role in the development of tumor cells. Soon after, we unexpectedly found that the expression of microRNA6778-5p (miR6778-5p) is unconventionally high in the gastric cancer cells low-expressing Drosha. So, we designed the Drosha interference sequence and recombined it into a lentiviral vector to construct Drosha knockdown lentivirus and transfected the Drosha knockdown lentivirus into gastric cancer cells to establish Drosha knockdown gastric cancer cell lines. We aimed to explore the effect of microRNA6778-5p on the proliferation of gastric cancer cells with Drosha knockdown and its intrinsic mechanism. Methods: We designed the Drosha interference sequence and recombined it into a lentiviral vector to construct Drosha knockdown lentivirus and transfected the Drosha knockdown lentivirus into gastric cancer cells to establish Drosha knockdown gastric cancer cell lines. After transfecting miR6778-5p mimics and inhibitor into gastric cancer cell lines with Drosha knockdown, the expression levels of miR6778-5p mimics in Drosha low-expressing gastric cancer cells increased, while miR6778-5p inhibitor decreased the expression levels of miR6778-5p. The Cell Counting Kit-8 (CCK-8) experiment was used to detect the proliferation ability of gastric cancer cells after overexpression or knockdown of miR6778-5p and bioinformatics predicted the relationship between miR6778-5p and glycogen synthase kinase-3 Results: After infection with the Drosha knockdown lentivirus, Drosha's mRNA and protein levels were significantly downregulated in gastric cancer cells. The expression levels of miR6778-5p mimics in Drosha low-expressing gastric cancer cells increased, while miR6778-5p inhibitor decreased the expression levels of miR6778-5p. Overexpression of miR6778-5p significantly enhanced the proliferation ability of Drosha low-expression gastric cancer cells; on the contrary, knocking down miR6778-5p weakened the proliferation ability of Drosha low-expression gastric cancer cells. Bioinformatics predicted that miR6778-5p targeted glycogen synthase kinase-3 Conclusion: miR6778-5p promotes the proliferation of Drosha low-expressing gastric cancer cells by targeting GSK3

Indexed as

MicroRNAsStomach NeoplasmsCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticGlycogen Synthase Kinase 3 betaHumansRibonuclease IIIRNA, MessengerDROSHA protein, humanGlycogen Synthase Kinase 3 betaMicroRNAsRibonuclease IIIRNA, Messenger

Identifiers

PMID36210981
PMCPMC9546646
OpenAlexW4298108692

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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.