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Clinically Applicable Inhibitors Impacting Genome Stability
Advances in technology have facilitated the molecular profiling (genomic and transcriptomic) of tumours, and has led to improved stratification of patients and the individualisation of treatment regimes. To fully realize the potential of truly personalised treatment options, we need targeted therapi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100577/ https://www.ncbi.nlm.nih.gov/pubmed/29757235 http://dx.doi.org/10.3390/molecules23051166 |
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author | Prakash, Anu Garcia-Moreno, Juan F. Brown, James A. L. Bourke, Emer |
author_facet | Prakash, Anu Garcia-Moreno, Juan F. Brown, James A. L. Bourke, Emer |
author_sort | Prakash, Anu |
collection | PubMed |
description | Advances in technology have facilitated the molecular profiling (genomic and transcriptomic) of tumours, and has led to improved stratification of patients and the individualisation of treatment regimes. To fully realize the potential of truly personalised treatment options, we need targeted therapies that precisely disrupt the compensatory pathways identified by profiling which allow tumours to survive or gain resistance to treatments. Here, we discuss recent advances in novel therapies that impact the genome (chromosomes and chromatin), pathways targeted and the stage of the pathways targeted. The current state of research will be discussed, with a focus on compounds that have advanced into trials (clinical and pre-clinical). We will discuss inhibitors of specific DNA damage responses and other genome stability pathways, including those in development, which are likely to synergistically combine with current therapeutic options. Tumour profiling data, combined with the knowledge of new treatments that affect the regulation of essential tumour signalling pathways, is revealing fundamental insights into cancer progression and resistance mechanisms. This is the forefront of the next evolution of advanced oncology medicine that will ultimately lead to improved survival and may, one day, result in many cancers becoming chronic conditions, rather than fatal diseases. |
format | Online Article Text |
id | pubmed-6100577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61005772018-11-13 Clinically Applicable Inhibitors Impacting Genome Stability Prakash, Anu Garcia-Moreno, Juan F. Brown, James A. L. Bourke, Emer Molecules Review Advances in technology have facilitated the molecular profiling (genomic and transcriptomic) of tumours, and has led to improved stratification of patients and the individualisation of treatment regimes. To fully realize the potential of truly personalised treatment options, we need targeted therapies that precisely disrupt the compensatory pathways identified by profiling which allow tumours to survive or gain resistance to treatments. Here, we discuss recent advances in novel therapies that impact the genome (chromosomes and chromatin), pathways targeted and the stage of the pathways targeted. The current state of research will be discussed, with a focus on compounds that have advanced into trials (clinical and pre-clinical). We will discuss inhibitors of specific DNA damage responses and other genome stability pathways, including those in development, which are likely to synergistically combine with current therapeutic options. Tumour profiling data, combined with the knowledge of new treatments that affect the regulation of essential tumour signalling pathways, is revealing fundamental insights into cancer progression and resistance mechanisms. This is the forefront of the next evolution of advanced oncology medicine that will ultimately lead to improved survival and may, one day, result in many cancers becoming chronic conditions, rather than fatal diseases. MDPI 2018-05-13 /pmc/articles/PMC6100577/ /pubmed/29757235 http://dx.doi.org/10.3390/molecules23051166 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Prakash, Anu Garcia-Moreno, Juan F. Brown, James A. L. Bourke, Emer Clinically Applicable Inhibitors Impacting Genome Stability |
title | Clinically Applicable Inhibitors Impacting Genome Stability |
title_full | Clinically Applicable Inhibitors Impacting Genome Stability |
title_fullStr | Clinically Applicable Inhibitors Impacting Genome Stability |
title_full_unstemmed | Clinically Applicable Inhibitors Impacting Genome Stability |
title_short | Clinically Applicable Inhibitors Impacting Genome Stability |
title_sort | clinically applicable inhibitors impacting genome stability |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100577/ https://www.ncbi.nlm.nih.gov/pubmed/29757235 http://dx.doi.org/10.3390/molecules23051166 |
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