Evidence map›Paper›PMID 31119871›Full record

ArticleJournal of cellular and molecular medicine2019

Long non-coding RNA SNHG6 promotes cell proliferation and migration through sponging miR-4465 in ovarian clear cell carcinoma.

Yong Wu, Yu Deng, Qinhao Guo, Jun Zhu, Lijie Cao, Xueqi Guo, Fei Xu, Weiwei Weng, Xingzhu Ju, Xiaohua Wu

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 3 pooled it
3.1field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 3 syntheses or guidelines pooled it, 57 citations in OpenAlex.

  1. Pooled it
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  9. LncRNA SNHG6 role in clinicopathological parameters in cancers.European journal of medical research · 2023
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  19. Emerging Roles of LncRNAs in the EZH2-regulated Oncogenic Network.International journal of biological sciences · 2021
    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

10 authors at 1 institution in 1 country.

Yong WuDepartment of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.
Yu DengDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, People's Republic of China.
Qinhao GuoDepartment of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.
Jun ZhuDepartment of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.
Lijie CaoDepartment of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.
Xueqi GuoDepartment of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.
Fei XuDepartment of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.
Weiwei WengDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, People's Republic of China.ORCID 0000-0002-2964-5836
Xingzhu JuDepartment of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.
Xiaohua WuDepartment of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.ORCID 0000-0002-6889-3541
Shanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulation of small nucleolar RNA host gene 6 (SNHG6) exerts critical oncogenic effects and facilitates tumourigenesis in human cancers. However, little information about the expression pattern of SNHG6 in ovarian clear cell carcinoma (OCCC) is available, and the contributions of this long non-coding RNA to the tumourigenesis and progression of OCCC are unclear. In the present study, we showed via quantitative real-time PCR that SNHG6 expression was abnormally up-regulated in OCCC tissues relative to that in unpaired normal ovarian tissues. High SNHG6 expression was correlated with vascular invasion, distant metastasis and poor survival. Further functional experiments demonstrated that knockdown of SNHG6 in OCCC cells inhibited cell proliferation, migration and invasion in vitro as well as tumour growth in vivo. Moreover, SNHG6 functioned as a competing endogenous RNA (ceRNA), effectively acting as a sponge for miR-4465 and thereby modulating the expression of enhancer of zeste homolog 2 (EZH2). Taken together, our data suggest that SNHG6 is a novel molecule involved in OCCC progression and that targeting the ceRNA network involving SNHG6 may be a treatment strategy in OCCC.

Indexed as

AnimalsCarcinogenesisCarcinomaCell Line, TumorCell MovementCell ProliferationEnhancer of Zeste Homolog 2 ProteinFemaleHumansMiceMice, Inbred BALB CMice, NudeMicroRNAsMiddle AgedOvarian NeoplasmsPrognosisEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanlong non-coding RNA SNHG6, humanMicroRNAsRNA, Long Noncodingcell migrationEZH2miR-4465ovarian clear cell carcinomaSNHG6

Identifiers

PMID31119871
PMCPMC6653241
OpenAlexW2946476051

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.