Evidence map›Paper›PMID 26910911›Full record

ArticleOncotarget2016

MicroRNA-27b up-regulated by human papillomavirus 16 E7 promotes proliferation and suppresses apoptosis by targeting polo-like kinase2 in cervical cancer.

Fei Liu, Shimeng Zhang, Zhen Zhao, Xinru Mao, Jinlan Huang, Zixian Wu, Lei Zheng, Qian Wang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 70 citations in OpenAlex.

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  14. Cell death pathways and viruses: Role of microRNAs.Molecular therapy. Nucleic acids · 2021
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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 3 institutions in 2 countries.

Fei LiuDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Shimeng ZhangDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Zhen ZhaoDepartment of Laboratory Medicine, NIH Clinical Center, Bethesda, MD 20892, USA.
Xinru MaoDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Jinlan HuangDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Zixian WuDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Lei ZhengDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Qian WangDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Nanfang Hospital · CNSouthern Medical University · CNNational Institutes of Health Clinical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The infection with high-risk human papillomavirus is linked to cervical cancer, nevertheless, the role of miRNAs regulated by HPV oncogenes in cancer progression remain largely unknown. Here, we knocked down endogenous E6/E7 in HPV16-positive CaSki cell lines, screened differences in miRNA expression profile with control using miRNA array. 38 miRNAs were down-regulated and 6 miRNAs were up-regulated in the E6/E7 silenced CaSki cells (>2-fold changes with P <0.05). The levels of miR-27b, miR-20a, miR-24, miR-93, and miR-106b were verified by qPCR in E6/E7 silenced CaSki and SiHa cells. MiR-27b, up-regulated by E7, promoted CaSki and SiHa cell proliferation and invasion, inhibit paclitaxel-induced apoptosis. Dual-luciferase experiment confirmed miR-27b down-regulated its target gene PLK2 through the "seed regions". The tumor suppressor PLK2 inhibited SiHa cell proliferation, reduced cell viability, and promoted paclitaxel/cisplatin -induced apoptosis. Furthermore, DGCR8 was found to mediate the up-regulation of miR-27b by HPV16 E7. Our study demonstrated that HPV16 E7 could increase DGCR8 to promote the generation of miR-27b, which accelerated cell proliferation and inhibited paclitaxel-induced cell apoptosis through down-regulating PLK2. These findings provide an insight into the interaction network of viral oncogene, miR-27b and PLK2, and support the potential strategies using antisense nucleic acid of miR-27b for therapy of cervical cancer in the future.

Indexed as

ApoptosisBlotting, WesternCell Line, TumorCell ProliferationFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHost-Pathogen InteractionsHuman papillomavirus 16HumansMicroRNAsPapillomavirus E7 ProteinsProtein Serine-Threonine KinasesRNA-Binding ProteinsRNA InterferenceUp-RegulationDGCR8 protein, humanMicroRNAsMIRN27 microRNA, humanoncogene protein E7, Human papillomavirus type 16Papillomavirus E7 ProteinsPLK2 protein, humanProtein Serine-Threonine KinasesRNA-Binding Proteinscervical cancerDGCR8HPV16 E7microRNA-27bpolo-like kinase2

Identifiers

PMID26910911
PMCPMC4991410
OpenAlexW2289358625

What OpenQuestion holds

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LicenceCC BY
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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.