Evidence map›Paper›PMID 31410981›Full record

ArticleFEBS open bio2019

MicroRNA-488 inhibits proliferation and glycolysis in human prostate cancer cells by regulating PFKFB3.

Jun Wang, Xiaojuan Li, Zhaoming Xiao, Yu Wang, Yuefu Han, Jun Li, Weian Zhu, Qu Leng, Yuehui Wen, Xinqiao Wen

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  4. Article
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  7. Article
  8. Reference Genes for qPCR-Based miRNA Expression Profiling in 14 Human Tissues.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 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

10 authors at 5 institutions in 1 country.

Jun WangDepartment of Urology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0001-8074-789X
Xiaojuan LiCenter of Health Management, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Zhaoming XiaoDepartment of Urology, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Yu WangDepartment of Urology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yuefu HanDepartment of Urology, Yue Bei People's Hospital, Shaoguan, China.
Jun LiDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Weian ZhuDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Qu LengDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Yuehui WenDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Xinqiao WenDepartment of Urology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Southern Medical University Shenzhen Hospital · CNSun Yat-sen University · CNNanfang Hospital · CNShanghai Medical College of Fudan University · CNShantou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer (PCa) remains the second leading cause of cancer-related death among men in the United States, and its molecular mechanism remains to be elucidated. Recent studies have suggested that microRNAs may play an important role in cancer development and progression. By analyzing the Gene Expression Omnibus dataset, we found lower expression for miR-488 in PCa than in normal tissues. Moreover, CCK-8, EdU, glucose uptake, and lactate secrete assays revealed that overexpression of miR-488 in PCa cell lines PC3 and DU145 resulted in inhibition of proliferation and glycolysis. In contrast, downregulation of miR-488 expression promoted proliferation and glycolysis in PCa cells. Using a bioinformatic approach and dual-luciferase reporter assays, we identified 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase, isoform3 (PFKFB3), as a direct target of miR-488. Inhibition of PFKFB3 also suppressed PCa cell glycolysis and proliferation. Our study suggests that miR-488 inhibits PCa cell proliferation and glycolysis by targeting PFKFB3, and thus, miR-488 may be a novel therapeutic candidate for PCa.

Indexed as

ApoptosisCell MovementCell ProliferationDown-RegulationGlycolysisHumansMaleMicroRNAsPhosphofructokinase-2Prostatic NeoplasmsTumor Cells, CulturedMicroRNAsMIRN488 microRNA, humanPFKFB3 protein, humanPhosphofructokinase-2glycolysismiR-488PFKFB3proliferationprostate cancer cell

Identifiers

PMID31410981
PMCPMC6768114
OpenAlexW2967740083

What OpenQuestion holds

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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.