Evidence map›Paper›PMID 34793263›Full record

ArticleBioengineered2021

The miRNA mir-582-3p suppresses ovarian cancer progression by targeting AKT/MTOR signaling

Tianyu Dai, Junhui Liang, Wei Liu, Yonghui Zou, Feifei Niu, Mengqing Li, Haomeng Zhang, Changzhong Li, Mingjun Fan, Guoying Cui

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 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. The regulatory role ofOncology research · 2025
    Pooled it
  2. Article
  3. The multifaceted roles of ribosomal P complex in cancer.World journal of surgical oncology · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Frontiers in pharmacology · 2022
    Article
  13. Review
  14. Article
  15. Article
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.

Tianyu DaiDepartment of Gynecology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Junhui LiangDepartment of Gynecology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Wei LiuDepartment of Gynecology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Yonghui ZouDepartment of Gynecology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Feifei NiuDepartment of Gynecology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Mengqing LiDepartment of Gynecology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Haomeng ZhangDepartment of Gynecology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Changzhong LiDepartment of Gynecology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Mingjun FanDepartment of Gynecology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Guoying CuiDepartment of Gynecology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Shandong Provincial Hospital · CNShandong University · CNShandong First Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer (OC) is one of the most common malignancies of the female reproductive system. The miRNA miR-582-3p is associated with a variety of tumors, and the aim of this study was to investigate the role and mechanisms of miR-582-3p specifically in ovarian carcinogenesis and progression. Low expression of miR-582-3p was noted in OC tissue and cell lines, and lower expression of miR-582-3p correlated with lower overall survival in OC patients. Knockdown of miR-582-3p promoted the proliferation and migration of OC cells, while overexpression inhibited them. TUG1, a long non-coding RNA, was found to bind to miR-582-3p, and inhibition of lncRNA TUG1 decreased viability and migration and weakened the effect of miR-582-3p knockdown in OC cells. Implantation of OC cells with reduced miR-582-3p caused increased tumor growth, while lncRNA TUG1 knockdown suppressed tumor growth and relieved the impact of reduced miR-582-3p

Indexed as

AnimalsApoptosisCarcinogenesisCarcinoma, Ovarian EpithelialCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMiceMice, NudeMicroRNAsOvarian NeoplasmsProto-Oncogene Proteins c-aktRNA, Long NoncodingMicroRNAsMIRN582 microRNA, humanMTOR protein, humanProto-Oncogene Proteins c-aktRNA, Long NoncodingTOR Serine-Threonine KinasesTUG1 long noncoding RNA, humanAKT/mTOR signaling pathwaylncRNA TUG1miR-582-3povarian cancer

Identifiers

PMID34793263
PMCPMC8810093
OpenAlexW3211670342

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.