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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...

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Autores principales: Yang, Haitao, Jaeger, MariaLynn, Walker, Averi, Wei, Daniel, Leiker, Katie, Weitao, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
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.
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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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