Evidence map›Paper›PMID 31332950›Full record

ArticleThe Kaohsiung journal of medical sciences2019

MicroRNA-498 promotes proliferation, migration, and invasion of prostate cancer cells and decreases radiation sensitivity by targeting PTEN.

Xiu-Mei Duan, Xiao-Na Liu, Yu-Xin Li, Yu-Qing Cao, Aidaeraili Silayiding, Rong-Kui Zhang, Ji-Ping Wang

Abstract read
In one paragraph

Article in The Kaohsiung journal of medical sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Review
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  10. Review
  11. MicroRNA: a novel implication for damage and protection against ionizing radiation.Environmental science and pollution research international · 2021
    Review
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  13. Review
  14. Observational
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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

7 authors.

Xiu-Mei DuanDepartment of Pathology, The First Hospital, Jilin University, China.
Xiao-Na LiuDepartment of Pathology, The First Hospital, Jilin University, China.
Yu-Xin LiDepartment of Pathology, The First Hospital, Jilin University, China.
Yu-Qing CaoDepartment of Pathology, The First Hospital, Jilin University, China.
Aidaeraili SilayidingDepartment of Pathology, The First Hospital, Jilin University, China.
Rong-Kui ZhangDepartment of Radiology, The First Hospital, Jilin University, China.
Ji-Ping WangDepartment of Radiology, The First Hospital, Jilin University, China.ORCID https://orcid.org/0000-0003-2764-487X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer (PCa) remains the secondary highest cause of cancer-related death in the United States in men. It has been reported that microRNAs can serve as key regulators in tumor development and progression in various cancers including PCa. In this study, we examined the effect of miR-498 on proliferation, radiosensitivity, invasion, and migration of PCa cells. The proliferation of LNCaP and DU-145 PCa cells with altered expression of miR-498 was evaluated by MTT assay. The invasion and migration of LNCaP and DU-145 PCa cells were assess by matrigel invasion assay and transwell migration assay. The protein expression level in PCa cells was examined by western blot. The function of miR-498 on radiation-induced apoptosis in LNCaP and DU-145 PCa cells was detected by Caspase-Glo3/7 assay. Forced expression of miR-498 improved the proliferation, invasion and migration in PCa cells. Furthermore, miR-498 decreased the sensitivity of PCa cells after ionizing radiation treatment. MiR-498 reduced the radiation-induced apoptosis in PCa cells by regulation of BAX and Bcl-2 expression. Meanwhile, miR-498 altered the expression of E-cadherin, N-cadherin, snail, and Vimentin in both LNCaP and DU-145 PCa cells and regulated epithelial to mesenchymal transition (EMT). Further study showed that aberrant expression of miR-498 changed the expression levels of phosphatase and tensin homolog and p-AKT in LNCaP and DU-145 PCa cells. In a summary, miR-498 displayed important roles in tumor development and progression in PCa cells, and might act as a potential prognostic biomarker and predict radiotherapy response in PCa.

Indexed as

3' Untranslated RegionsApoptosisBase SequenceBiomarkers, TumorCell Line, TumorCell MovementCell ProliferationCell SurvivalDown-RegulationEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansMaleMicroRNAsNeoplasm InvasivenessProstatic Neoplasms3' Untranslated RegionsBiomarkers, TumorMicroRNAsMIRN498 microRNA, humanProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanAKTapoptosismiR-498prostate cancer

Identifiers

PMID31332950
PMCPMC11900769

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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.