Evidence map›Paper›PMID 32428870›Full record

ArticleAging2020

lncRNA OGFRP1 functions as a ceRNA to promote the progression of prostate cancer by regulating SARM1 level via miR-124-3p.

Keqiang Yan, Lifang Hou, Tiantian Liu, Wei Jiao, Qian Ma, Zhiqing Fang, Shimin Zhang, Daoqing Song, Jikai Liu, Xinghua Gao and 1 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Regulation of TIR-1/SARM-1 by miR-71 Protects Dopaminergic Neurons in aInternational journal of molecular sciences · 2024
    Article
  8. Review
  9. HRCT1, negatively regulated by miR-124-3p, promotes tumor metastasis and the growth of gastric cancer by activating the ERBB2-MAPK pathway.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2023
    Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. EpCAM as a Novel Biomarker for Survivals in Prostate Cancer Patients.Frontiers in cell and developmental biology · 2022
    Article
  18. Article
  19. Article
  20. 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

11 authors at 3 institutions in 1 country.

Keqiang YanDepartment of Urology, QiLu Hospital of Shandong University, Jinan 250012, Shandong, P.R. China.
Lifang HouDepartment of Gynecology, Jinan Central Hospital, Jinan 250012, Shandong, P.R. China.
Tiantian LiuPathology department, Basic Mmedical School, Shandong University, Jinan 250012, Shandong, P.R. China.
Wei JiaoDepartment of Urology, QiLu Hospital of Shandong University, Jinan 250012, Shandong, P.R. China.
Qian MaDepartment of Urology, QiLu Hospital of Shandong University, Jinan 250012, Shandong, P.R. China.
Zhiqing FangDepartment of Urology, QiLu Hospital of Shandong University, Jinan 250012, Shandong, P.R. China.
Shimin ZhangDepartment of Urology, Jinan Central Hospital Affiliated to Shandong First Medical University, Jinan 250012, Shandong, P.R. China.
Daoqing SongDepartment of Urology, QiLu Hospital of Shandong University, Jinan 250012, Shandong, P.R. China.
Jikai LiuDepartment of Urology, QiLu Hospital of Shandong University, Jinan 250012, Shandong, P.R. China.
Xinghua GaoDepartment of Urology, Jinan Central Hospital Affiliated to Shandong First Medical University, Jinan 250012, Shandong, P.R. China.
Yidong FanDepartment of Urology, QiLu Hospital of Shandong University, Jinan 250012, Shandong, P.R. China.
Qilu Hospital of Shandong University · CNJinan Central Hospital · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

lncRNA can interact with miRNA as a ceRNA to participate in the regulation of target gene expression, thus playing an important role in the development of malignant tumors. In this research, we found that OGFRP1 was up-regulated in prostate cancer (PCa) clinical samples and cell lines. Additionally, OGFRP1 is significantly associated with TNM stages III and IV and perineural invasion. Knockdown of OGFRP1 inhibited the growth of PCa cells, suggesting a promotional effect of OGFRP1 in tumor progression. Interestingly, OGFRP1 primarily localized in the cytoplasm, while miR-124-3p was found to bind to OGFRP1. Therefore, we further analyzed the downstream target of miR-124-3p using TargetScan. The result of the luciferase reporter gene assay displayed that SARM1 was a downstream target of miR-124-3p in two PCa cell lines. The overexpression of SARM1 promoted growth and metastasis in PCa cells. Knockdown of OGFRP1 and overexpression of miR-124-3p markedly restored the promotion of SARM1 to PCa cells. In conclusion, lncRNA OGFRP1 completely bound to miR-124-3p and relieved their inhibition on SARM1, thus promoting the growth of PCa cells. This report extended our understanding of the underlying molecular mechanisms of lncRNAs in PCa, which could help us find novel diagnostic and therapeutic targets.

Indexed as

Armadillo Domain ProteinsCytoskeletal ProteinsMicroRNAsProstatic NeoplasmsRNA, Long NoncodingCell Line, TumorDisease ProgressionHumansMaleArmadillo Domain ProteinsCytoskeletal ProteinsMicroRNAsMIRN1243 microRNA, humanRNA, Long NoncodingSARM1 protein, humanceRNAlong non-coding RNAsmiR-124-3pprostate cancerSARM1

Identifiers

PMID32428870
PMCPMC7288971
OpenAlexW3028488594

What OpenQuestion holds

Textmetadata
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.