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Identification of cancer driver genes using Sleeping Beauty transposon mutagenesis

Cancer genome sequencing studies have identified driver genes for a variety of different cancers and helped to understand the genetic landscape of human cancer. It is still challenging, however, to identify cancer driver genes with confidence simply from genetic data alone. In vivo forward genetic s...

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Autores principales: Takeda, Haruna, Jenkins, Nancy A., Copeland, Neal G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177796/
https://www.ncbi.nlm.nih.gov/pubmed/33783919
http://dx.doi.org/10.1111/cas.14901
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author Takeda, Haruna
Jenkins, Nancy A.
Copeland, Neal G.
author_facet Takeda, Haruna
Jenkins, Nancy A.
Copeland, Neal G.
author_sort Takeda, Haruna
collection PubMed
description Cancer genome sequencing studies have identified driver genes for a variety of different cancers and helped to understand the genetic landscape of human cancer. It is still challenging, however, to identify cancer driver genes with confidence simply from genetic data alone. In vivo forward genetic screens using Sleeping Beauty (SB) transposon mutagenesis provides another powerful genetic tool for identifying candidate cancer driver genes in wild‐type and sensitized mouse tumors. By comparing cancer driver genes identified in human and mouse tumors, cancer driver genes can be identified with additional confidence based upon comparative oncogenomics. This review describes how SB mutagenesis works in mice and focuses on studies that have identified cancer driver genes in the mouse gastrointestinal tract.
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spelling pubmed-81777962021-06-15 Identification of cancer driver genes using Sleeping Beauty transposon mutagenesis Takeda, Haruna Jenkins, Nancy A. Copeland, Neal G. Cancer Sci Review Articles Cancer genome sequencing studies have identified driver genes for a variety of different cancers and helped to understand the genetic landscape of human cancer. It is still challenging, however, to identify cancer driver genes with confidence simply from genetic data alone. In vivo forward genetic screens using Sleeping Beauty (SB) transposon mutagenesis provides another powerful genetic tool for identifying candidate cancer driver genes in wild‐type and sensitized mouse tumors. By comparing cancer driver genes identified in human and mouse tumors, cancer driver genes can be identified with additional confidence based upon comparative oncogenomics. This review describes how SB mutagenesis works in mice and focuses on studies that have identified cancer driver genes in the mouse gastrointestinal tract. John Wiley and Sons Inc. 2021-05-01 2021-06 /pmc/articles/PMC8177796/ /pubmed/33783919 http://dx.doi.org/10.1111/cas.14901 Text en © 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review Articles
Takeda, Haruna
Jenkins, Nancy A.
Copeland, Neal G.
Identification of cancer driver genes using Sleeping Beauty transposon mutagenesis
title Identification of cancer driver genes using Sleeping Beauty transposon mutagenesis
title_full Identification of cancer driver genes using Sleeping Beauty transposon mutagenesis
title_fullStr Identification of cancer driver genes using Sleeping Beauty transposon mutagenesis
title_full_unstemmed Identification of cancer driver genes using Sleeping Beauty transposon mutagenesis
title_short Identification of cancer driver genes using Sleeping Beauty transposon mutagenesis
title_sort identification of cancer driver genes using sleeping beauty transposon mutagenesis
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177796/
https://www.ncbi.nlm.nih.gov/pubmed/33783919
http://dx.doi.org/10.1111/cas.14901
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