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The micro RNA hsa-miR-377-3p inhibits tumor growth in malignant melanoma
Background/Aims: Most recently, micro RNAs (miRNAs/miRs) have been suggested to play a key role in various physiological and pathological processes by regulating the expression of specific genes. The influence of miR-377-3p on multitudinous cancer cells has been investigated; however, its function i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065064/ https://www.ncbi.nlm.nih.gov/pubmed/35516861 http://dx.doi.org/10.1039/c9ra02816a |
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author | Yuan, Jian Jiang, Lei Guo, Chaotang |
author_facet | Yuan, Jian Jiang, Lei Guo, Chaotang |
author_sort | Yuan, Jian |
collection | PubMed |
description | Background/Aims: Most recently, micro RNAs (miRNAs/miRs) have been suggested to play a key role in various physiological and pathological processes by regulating the expression of specific genes. The influence of miR-377-3p on multitudinous cancer cells has been investigated; however, its function in melanoma remains undiscovered. Armadillo repeat-containing protein 8 (ARMC8), a target of miR-377-3p, plays essential roles in proliferation, differentiation and apoptosis. Our research aimed to detect the specific roles of miR-377-3p in melanoma. Methods: The MiRNA and mRNA expressions were evaluated by a real-time quantitative polymerase chain reaction in the A375 and HEMa-LP cell lines. We predicted the possible interactions between microRNA and mRNAs by bioinformatics database and constructed them with the Cytoscape software. The proliferation and migration activities were investigated using a cell counting kit-8 (CCK8) and wound-healing assay. Validation of the correlation between miR-377-3p and ARMC8 was implemented by the luciferase reporter assay and PCR. Results: The expression of miR-377-3p was found to be lower in malignant melanoma cells. The upregulation of miR-377-3p inhibited the melanoma cell proliferation, migration, and ARMC8 expression. miR-377-3p was identified to bind to the 3′UTR region of ARMC8 directly; this indicated that miR-377-3p suppressed melanoma cell growth partly mediated via the ARMC8 expression. Conclusion: These findings show that miR-377-3p negatively regulates tumor growth in malignant melanoma, which may thus provide a potential biological target for melanoma treatment and subsequently lead to the development of potential treatments. |
format | Online Article Text |
id | pubmed-9065064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90650642022-05-04 The micro RNA hsa-miR-377-3p inhibits tumor growth in malignant melanoma Yuan, Jian Jiang, Lei Guo, Chaotang RSC Adv Chemistry Background/Aims: Most recently, micro RNAs (miRNAs/miRs) have been suggested to play a key role in various physiological and pathological processes by regulating the expression of specific genes. The influence of miR-377-3p on multitudinous cancer cells has been investigated; however, its function in melanoma remains undiscovered. Armadillo repeat-containing protein 8 (ARMC8), a target of miR-377-3p, plays essential roles in proliferation, differentiation and apoptosis. Our research aimed to detect the specific roles of miR-377-3p in melanoma. Methods: The MiRNA and mRNA expressions were evaluated by a real-time quantitative polymerase chain reaction in the A375 and HEMa-LP cell lines. We predicted the possible interactions between microRNA and mRNAs by bioinformatics database and constructed them with the Cytoscape software. The proliferation and migration activities were investigated using a cell counting kit-8 (CCK8) and wound-healing assay. Validation of the correlation between miR-377-3p and ARMC8 was implemented by the luciferase reporter assay and PCR. Results: The expression of miR-377-3p was found to be lower in malignant melanoma cells. The upregulation of miR-377-3p inhibited the melanoma cell proliferation, migration, and ARMC8 expression. miR-377-3p was identified to bind to the 3′UTR region of ARMC8 directly; this indicated that miR-377-3p suppressed melanoma cell growth partly mediated via the ARMC8 expression. Conclusion: These findings show that miR-377-3p negatively regulates tumor growth in malignant melanoma, which may thus provide a potential biological target for melanoma treatment and subsequently lead to the development of potential treatments. The Royal Society of Chemistry 2019-06-17 /pmc/articles/PMC9065064/ /pubmed/35516861 http://dx.doi.org/10.1039/c9ra02816a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Yuan, Jian Jiang, Lei Guo, Chaotang The micro RNA hsa-miR-377-3p inhibits tumor growth in malignant melanoma |
title | The micro RNA hsa-miR-377-3p inhibits tumor growth in malignant melanoma |
title_full | The micro RNA hsa-miR-377-3p inhibits tumor growth in malignant melanoma |
title_fullStr | The micro RNA hsa-miR-377-3p inhibits tumor growth in malignant melanoma |
title_full_unstemmed | The micro RNA hsa-miR-377-3p inhibits tumor growth in malignant melanoma |
title_short | The micro RNA hsa-miR-377-3p inhibits tumor growth in malignant melanoma |
title_sort | micro rna hsa-mir-377-3p inhibits tumor growth in malignant melanoma |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065064/ https://www.ncbi.nlm.nih.gov/pubmed/35516861 http://dx.doi.org/10.1039/c9ra02816a |
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