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Oncology Reports
Article
License: CC BY NC ND
Data sources: UnpayWall
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PubMed Central
Other literature type . 2018
Data sources: PubMed Central
Oncology Reports
Article . 2018 . Peer-reviewed
Data sources: Crossref
Oncology Reports
Article . 2018
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miR‑590‑5p inhibits tumor growth in malignant melanoma by suppressing YAP1 expression

Authors: Mou, Kuanhou; Ding, Meiling; Han, Dan; Zhou, Yan; Mu, Xin; Liu, Wenli; Wang, Lijuan;

miR‑590‑5p inhibits tumor growth in malignant melanoma by suppressing YAP1 expression

Abstract

The microRNAs (miRNAs/miRs) involved in the carcinogenesis and progression of malignant melanoma (MM) remain unclear. In the present study, miR‑590‑5p was identified to be upregulated in MM cells compared with human melanocytes using a reverse transcription‑quantitative polymerase chain reaction to screen established oncogenic and tumor suppressor miRNAs. miR‑590‑5p was demonstrated to inhibit the cell proliferation and tumor growth of MM cells in vitro and in vivo by performing Cell Counting Kit‑8 and tumour xenograft assays, respectively. In addition, flowcytometry assays indicated that miR‑590‑5p induced cell apoptosis and cell cycle arrest at the G1 stage in MM cells. Finally, luciferase assays and western blot analysis results confirmed that the transcriptional regulator Yes‑associated protein 1 (YAP1) is upregulated and inversely associated with miR‑590‑5p expression in MM cells, and is the direct target and functional mediator of miR‑590‑5p in MM. Altogether these results reveal the functional and mechanistic link between miR‑590‑5p and YAP1 in the progression of MM. Therefore, miR‑590‑5p is a potential therapeutic target in MM.

Keywords

Mice, Inbred BALB C, Cell Cycle, Mice, Nude, Apoptosis, YAP-Signaling Proteins, Articles, Phosphoproteins, Xenograft Model Antitumor Assays, Gene Expression Regulation, Neoplastic, Mice, MicroRNAs, Cell Movement, Biomarkers, Tumor, Tumor Cells, Cultured, Animals, Humans, Female, Melanoma, Adaptor Proteins, Signal Transducing, Cell Proliferation, Transcription Factors

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    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
10
Top 10%
Average
Top 10%
Green
hybrid