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In vivo miRNA knockout screening identifies miR-190b as a novel tumor suppressor
MicroRNAs (miRNAs) play important roles in the development of various cancers including lung cancer which is one of the devastating diseases worldwide. How miRNAs function in de novo lung tumorigenesis remains largely unknown. We here developed a CRISPR/Cas9-mediated dual guide RNA (dgRNA) system to...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660552/ https://www.ncbi.nlm.nih.gov/pubmed/33137086 http://dx.doi.org/10.1371/journal.pgen.1009168 |
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author | Hong, Hui Yao, Shun Zhang, Yuanyuan Ye, Yi Li, Cheng Hu, Liang Sun, Yihua Huang, Hsin-Yi Ji, Hongbin |
author_facet | Hong, Hui Yao, Shun Zhang, Yuanyuan Ye, Yi Li, Cheng Hu, Liang Sun, Yihua Huang, Hsin-Yi Ji, Hongbin |
author_sort | Hong, Hui |
collection | PubMed |
description | MicroRNAs (miRNAs) play important roles in the development of various cancers including lung cancer which is one of the devastating diseases worldwide. How miRNAs function in de novo lung tumorigenesis remains largely unknown. We here developed a CRISPR/Cas9-mediated dual guide RNA (dgRNA) system to knockout miRNAs in genetically engineered mouse model (GEMM). Through bioinformatic analyses of human lung cancer miRNA database, we identified 16 downregulated miRNAs associated with malignant progression and performed individual knockout with dgRNA system in Kras(G12D)/Trp53(L/L) (KP) mouse model. Using this in vivo knockout screening, we identified miR-30b and miR-146a, which has been previously reported as tumor suppressors and miR-190b, a new tumor-suppressive miRNA in lung cancer development. Over-expression of miR-190b in KP model as well as human lung cancer cell lines significantly suppressed malignant progression. We further found that miR-190b targeted the Hus1 gene and knockout of Hus1 in KP model dramatically suppressed lung tumorigenesis. Collectively, our study developed an in vivo miRNA knockout platform for functionally screening in GEMM and identified miR-190b as a new tumor suppressor in lung cancer. |
format | Online Article Text |
id | pubmed-7660552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-76605522020-11-18 In vivo miRNA knockout screening identifies miR-190b as a novel tumor suppressor Hong, Hui Yao, Shun Zhang, Yuanyuan Ye, Yi Li, Cheng Hu, Liang Sun, Yihua Huang, Hsin-Yi Ji, Hongbin PLoS Genet Research Article MicroRNAs (miRNAs) play important roles in the development of various cancers including lung cancer which is one of the devastating diseases worldwide. How miRNAs function in de novo lung tumorigenesis remains largely unknown. We here developed a CRISPR/Cas9-mediated dual guide RNA (dgRNA) system to knockout miRNAs in genetically engineered mouse model (GEMM). Through bioinformatic analyses of human lung cancer miRNA database, we identified 16 downregulated miRNAs associated with malignant progression and performed individual knockout with dgRNA system in Kras(G12D)/Trp53(L/L) (KP) mouse model. Using this in vivo knockout screening, we identified miR-30b and miR-146a, which has been previously reported as tumor suppressors and miR-190b, a new tumor-suppressive miRNA in lung cancer development. Over-expression of miR-190b in KP model as well as human lung cancer cell lines significantly suppressed malignant progression. We further found that miR-190b targeted the Hus1 gene and knockout of Hus1 in KP model dramatically suppressed lung tumorigenesis. Collectively, our study developed an in vivo miRNA knockout platform for functionally screening in GEMM and identified miR-190b as a new tumor suppressor in lung cancer. Public Library of Science 2020-11-02 /pmc/articles/PMC7660552/ /pubmed/33137086 http://dx.doi.org/10.1371/journal.pgen.1009168 Text en © 2020 Hong et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Hong, Hui Yao, Shun Zhang, Yuanyuan Ye, Yi Li, Cheng Hu, Liang Sun, Yihua Huang, Hsin-Yi Ji, Hongbin In vivo miRNA knockout screening identifies miR-190b as a novel tumor suppressor |
title | In vivo miRNA knockout screening identifies miR-190b as a novel tumor suppressor |
title_full | In vivo miRNA knockout screening identifies miR-190b as a novel tumor suppressor |
title_fullStr | In vivo miRNA knockout screening identifies miR-190b as a novel tumor suppressor |
title_full_unstemmed | In vivo miRNA knockout screening identifies miR-190b as a novel tumor suppressor |
title_short | In vivo miRNA knockout screening identifies miR-190b as a novel tumor suppressor |
title_sort | in vivo mirna knockout screening identifies mir-190b as a novel tumor suppressor |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660552/ https://www.ncbi.nlm.nih.gov/pubmed/33137086 http://dx.doi.org/10.1371/journal.pgen.1009168 |
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