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A Blue Light-Inducible CRISPR-Cas9 System for Inhibiting Progression of Melanoma Cells
Melanoma is an aggressive skin tumor that shows a high mortality rate and level of metastasis. BRAF gene mutation (BRAF V600E) is directly related to the occurrence of melanoma. In this study, a light-inducible gene expression system was designed to control the Cas9 transcription, which could then c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710612/ https://www.ncbi.nlm.nih.gov/pubmed/33330635 http://dx.doi.org/10.3389/fmolb.2020.606593 |
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author | Wu, Xia Huang, Haiyan Yu, Bo Zhang, Jianzhong |
author_facet | Wu, Xia Huang, Haiyan Yu, Bo Zhang, Jianzhong |
author_sort | Wu, Xia |
collection | PubMed |
description | Melanoma is an aggressive skin tumor that shows a high mortality rate and level of metastasis. BRAF gene mutation (BRAF V600E) is directly related to the occurrence of melanoma. In this study, a light-inducible gene expression system was designed to control the Cas9 transcription, which could then cleave the BRAF V600E. To prove the potential utility of this system in melanoma, the physiological function of melanoma cells was tested. It illustrated that the light-induced CRISPR-Cas9 system could inhibit the progression of G361 and A375 cells. Thus, this system may provide a novel therapeutic strategy of melanoma intervention. |
format | Online Article Text |
id | pubmed-7710612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77106122020-12-15 A Blue Light-Inducible CRISPR-Cas9 System for Inhibiting Progression of Melanoma Cells Wu, Xia Huang, Haiyan Yu, Bo Zhang, Jianzhong Front Mol Biosci Molecular Biosciences Melanoma is an aggressive skin tumor that shows a high mortality rate and level of metastasis. BRAF gene mutation (BRAF V600E) is directly related to the occurrence of melanoma. In this study, a light-inducible gene expression system was designed to control the Cas9 transcription, which could then cleave the BRAF V600E. To prove the potential utility of this system in melanoma, the physiological function of melanoma cells was tested. It illustrated that the light-induced CRISPR-Cas9 system could inhibit the progression of G361 and A375 cells. Thus, this system may provide a novel therapeutic strategy of melanoma intervention. Frontiers Media S.A. 2020-11-19 /pmc/articles/PMC7710612/ /pubmed/33330635 http://dx.doi.org/10.3389/fmolb.2020.606593 Text en Copyright © 2020 Wu, Huang, Yu and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Wu, Xia Huang, Haiyan Yu, Bo Zhang, Jianzhong A Blue Light-Inducible CRISPR-Cas9 System for Inhibiting Progression of Melanoma Cells |
title | A Blue Light-Inducible CRISPR-Cas9 System for Inhibiting Progression of Melanoma Cells |
title_full | A Blue Light-Inducible CRISPR-Cas9 System for Inhibiting Progression of Melanoma Cells |
title_fullStr | A Blue Light-Inducible CRISPR-Cas9 System for Inhibiting Progression of Melanoma Cells |
title_full_unstemmed | A Blue Light-Inducible CRISPR-Cas9 System for Inhibiting Progression of Melanoma Cells |
title_short | A Blue Light-Inducible CRISPR-Cas9 System for Inhibiting Progression of Melanoma Cells |
title_sort | blue light-inducible crispr-cas9 system for inhibiting progression of melanoma cells |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710612/ https://www.ncbi.nlm.nih.gov/pubmed/33330635 http://dx.doi.org/10.3389/fmolb.2020.606593 |
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