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Break Breast Cancer Addiction by CRISPR/Cas9 Genome Editing
Breast cancer is the leading diagnosed cancer for women globally. Evolution of breast cancer in tumorigenesis, metastasis and treatment resistance appears to be driven by the aberrant gene expression and protein degradation encoded by the cancer genomes. The uncontrolled cancer growth relies on thes...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771328/ https://www.ncbi.nlm.nih.gov/pubmed/29344267 http://dx.doi.org/10.7150/jca.22554 |
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author | Yang, Haitao Jaeger, MariaLynn Walker, Averi Wei, Daniel Leiker, Katie Weitao, Tao |
author_facet | Yang, Haitao Jaeger, MariaLynn Walker, Averi Wei, Daniel Leiker, Katie Weitao, Tao |
author_sort | Yang, Haitao |
collection | PubMed |
description | Breast cancer is the leading diagnosed cancer for women globally. Evolution of breast cancer in tumorigenesis, metastasis and treatment resistance appears to be driven by the aberrant gene expression and protein degradation encoded by the cancer genomes. The uncontrolled cancer growth relies on these cellular events, thus constituting the cancerous programs and rendering the addiction towards them. These programs are likely the potential anticancer biomarkers for Personalized Medicine of breast cancer. This review intends to delineate the impact of the CRSPR/Cas-mediated genome editing in identification and validation of these anticancer biomarkers. It reviews the progress in three aspects of CRISPR/Cas9-mediated editing of the breast cancer genomes: Somatic genome editing, transcription and protein degradation addictions. |
format | Online Article Text |
id | pubmed-5771328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-57713282018-01-17 Break Breast Cancer Addiction by CRISPR/Cas9 Genome Editing Yang, Haitao Jaeger, MariaLynn Walker, Averi Wei, Daniel Leiker, Katie Weitao, Tao J Cancer Review Breast cancer is the leading diagnosed cancer for women globally. Evolution of breast cancer in tumorigenesis, metastasis and treatment resistance appears to be driven by the aberrant gene expression and protein degradation encoded by the cancer genomes. The uncontrolled cancer growth relies on these cellular events, thus constituting the cancerous programs and rendering the addiction towards them. These programs are likely the potential anticancer biomarkers for Personalized Medicine of breast cancer. This review intends to delineate the impact of the CRSPR/Cas-mediated genome editing in identification and validation of these anticancer biomarkers. It reviews the progress in three aspects of CRISPR/Cas9-mediated editing of the breast cancer genomes: Somatic genome editing, transcription and protein degradation addictions. Ivyspring International Publisher 2018-01-01 /pmc/articles/PMC5771328/ /pubmed/29344267 http://dx.doi.org/10.7150/jca.22554 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Yang, Haitao Jaeger, MariaLynn Walker, Averi Wei, Daniel Leiker, Katie Weitao, Tao Break Breast Cancer Addiction by CRISPR/Cas9 Genome Editing |
title | Break Breast Cancer Addiction by CRISPR/Cas9 Genome Editing |
title_full | Break Breast Cancer Addiction by CRISPR/Cas9 Genome Editing |
title_fullStr | Break Breast Cancer Addiction by CRISPR/Cas9 Genome Editing |
title_full_unstemmed | Break Breast Cancer Addiction by CRISPR/Cas9 Genome Editing |
title_short | Break Breast Cancer Addiction by CRISPR/Cas9 Genome Editing |
title_sort | break breast cancer addiction by crispr/cas9 genome editing |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771328/ https://www.ncbi.nlm.nih.gov/pubmed/29344267 http://dx.doi.org/10.7150/jca.22554 |
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