Evidence map›Paper›PMID 36243865›Full record

ArticleJournal of ovarian research2022

Circular RNA hsa_circ_0000144 aggravates ovarian Cancer progression by regulating ELK3 via sponging miR-610.

Dandan Wu, Jia Liu, Liji Yu, Shaofang Wu, Xiaomei Qiu

Abstract read
In one paragraph

Article in Journal of ovarian research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Circular RNAs and Cancers.Advances in experimental medicine and biology · 2025
    Review
  4. Review
  5. Serum hsa_circ_0007534 as a diagnostic biomarker for ovarian cancer.American journal of translational research · 2024
    Article
  6. Review
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

5 authors.

Dandan WuDepartment of Obstetrics and Gynecology, The First Hospital of Quanzhou Affiliated to Fujian Medical University, Quanzhou, 362000, China. dandan28121@163.com.
Jia LiuDepartment of Obstetrics and Gynecology, The First Hospital of Quanzhou Affiliated to Fujian Medical University, Quanzhou, 362000, China.
Liji YuDepartment of Obstetrics and Gynecology, The First Hospital of Quanzhou Affiliated to Fujian Medical University, Quanzhou, 362000, China.
Shaofang WuDepartment of Obstetrics and Gynecology, The First Hospital of Quanzhou Affiliated to Fujian Medical University, Quanzhou, 362000, China.
Xiaomei QiuDepartment of Obstetrics and Gynecology, The First Hospital of Quanzhou Affiliated to Fujian Medical University, Quanzhou, 362000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOvarian cancer is a common cause of death among women and a health problem worldwide. Circ_0000144 has been confirmed to be an oncogene involved in cancer progression, such as gastric cancer. However, the role of circ_0000144 in ovarian cancer remains unclear and needs to be elucidated. This retrospective study aimed to investigate the underlying mechanism of circ_0000144 in ovarian cancer.

methodsDifferentially expressed circ_0000144 expression in ovarian cancer and normal tissues was identified by quantitative reverse transcriptase polymerase chain reaction (qRT-PCR). In vitro assays were performed to explore the biological functions of circ_0000144 in ovarian cancer cells. An in vivo xenograft model was used to investigate the efficacy of circ_0000144 in the progression of ovarian cancer.

resultsCirc_0000144 was significantly upregulated in ovarian cancer cells and tissues. Circ_0000144 overexpression significantly promoted ovarian cancer cell proliferation, migration, and invasion. This study further demonstrated that circ_0000144 downregulated ELK3 levels by sponging miR-610 in ovarian cancer cells. Moreover, circ_0000144 significantly promotes ovarian cancer tumorigenesis in vivo.

conclusionOur data indicate that circ_0000144 could enhance the carcinogenesis of ovarian cancer by specifically targeting miR-610, which may serve as a novel target for the diagnosis and prognosis of ovarian cancer.

Indexed as

MicroRNAsOvarian NeoplasmsCarcinogenesisCarcinoma, Ovarian EpithelialCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansProto-Oncogene Proteins c-etsRetrospective StudiesRNA, CircularElk3 protein, humanMicroRNAsMIRN610 microRNA, humanProto-Oncogene Proteins c-etsRNA, Circularcirc_0000144ELK3miR-610Ovarian cancerProliferation

Identifiers

PMID36243865
PMCPMC9569040

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.