Evidence map›Paper›PMID 33734009›Full record

ArticleBioengineered2021

Circular RNA ZNF609 functions as a competing endogenous RNA in regulating E2F transcription factor 6 through competitively binding to microRNA-197-3p to promote the progression of cervical cancer progression.

Qiao Gu, Wenjie Hou, Lijuan Shi, Huan Liu, Zonghao Zhu, Wenfeng Ye

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  12. The emerging roles of circRNAs in cancer and oncology.Nature reviews. Clinical oncology · 2022
    Review
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  19. Emerging Roles ofFrontiers in genetics · 2022
    Review
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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

6 authors at 3 institutions in 3 countries.

Qiao GuDepartment of Gynecology and Obstetrics, The Third Affiliated Hospital of Soochow University, Changzhou, P.R. China.
Wenjie HouDepartment of Gynecology and Obstetrics, Dushu Lake Hospital Affiliated to Soochow University (Medical Center of Soochow University), Suzhou, P.R. China.
Lijuan ShiDepartment of Gynecology and Obstetrics, The Third Affiliated Hospital of Soochow University, Changzhou, P.R. China.
Huan LiuDepartment of Pathology, Changzhou Hospital of Traditional Chinese Medicine, Changzhou, P.R. China.
Zonghao ZhuDepartment of Gynecology and Obstetrics, The Third Affiliated Hospital of Soochow University, Changzhou, P.R. China.
Wenfeng YeDepartment of Gynecology and Obstetrics, The Third Affiliated Hospital of Soochow University, Changzhou, P.R. China.ORCID 0000-0001-9694-8530
Soochow University · TWHangzhou Hospital of Traditional Chinese Medicine · CNUniversity Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Countless studies have demonstrated that Circular RNAs (circRNAs) exert vital effects in regulating tumorigenesis of various cancers. CircRNA ZNF609 (circ-ZNF609) has been reported as an oncogene in various human cancers. Nevertheless, its regulating effect in cervical cancer (CC) remains to be further explored. RT-qPCR was adopted to measure circ-ZNF609, miR-197-3p and E2F6 levels. CC cell proliferation, migration and invasion were analyzed via CCK-8 and transwell assays. Dual-luciferase reporter assay was adopted to confirm the interaction between miR-197-3p and circ-ZNF609 or E2F6. In the present study, it was found that circ-ZNF609 was elevated in CC tissues and cell lines, and circ-ZNF609 deletion repressed cell viability, migration and invasion in CC. Moreover, circ-ZNF609 was identified to negatively regulate miR-197-3p expression in CC cells. The inhibition of miR-197-3p abrogated the inhibitory effect on CC cell proliferation, migration and invasion induced by circ-ZNF609 knockdown. Additionally, we further demonstrated that circ-ZNF609 upregulated E2F6 by interacting with miR-197-3p. Finally, rescue assays indicated that E2F6 overexpression upended the suppression of CC progression induced by circ-ZNF609 deletion. In conclusion, circ-ZNF609 promoted CC progression through modulating the miR-197-3p/E2F6 axis as an oncogene. This finding offers a unique insight into CC molecular mechanism and suggests a potential target for CC therapy.

Indexed as

E2F6 Transcription FactorMicroRNAsRNA, CircularUterine Cervical NeoplasmsAnimalsCell Line, TumorCell ProliferationDisease ProgressionFemaleGene Knockdown TechniquesHumansMiceMice, Inbred BALB CMice, NudeReal-Time Polymerase Chain ReactionE2F6 protein, humanE2F6 Transcription FactorMicroRNAsMIRN197 microRNA, humanRNA, CircularccCirc-ZNF609e2f6miR-197-3pprogression

Identifiers

PMID33734009
PMCPMC8291891
OpenAlexW3138370230

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.