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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...

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Autores principales: Hong, Hui, Yao, Shun, Zhang, Yuanyuan, Ye, Yi, Li, Cheng, Hu, Liang, Sun, Yihua, Huang, Hsin-Yi, Ji, Hongbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
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.
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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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