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Targeted therapy: tailoring cancer treatment

Targeted therapies include small-molecule inhibitors and monoclonal antibodies, have made treatment more tumor-specific and less toxic, and have opened new possibilities for tailoring cancer treatment. Nevertheless, there remain several challenges to targeted therapies, including molecular identific...

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Detalles Bibliográficos
Autores principales: Yan, Min, Liu, Quentin Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sun Yat-sen University Cancer Center 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845608/
https://www.ncbi.nlm.nih.gov/pubmed/23823626
http://dx.doi.org/10.5732/cjc.013.10114
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author Yan, Min
Liu, Quentin Qiang
author_facet Yan, Min
Liu, Quentin Qiang
author_sort Yan, Min
collection PubMed
description Targeted therapies include small-molecule inhibitors and monoclonal antibodies, have made treatment more tumor-specific and less toxic, and have opened new possibilities for tailoring cancer treatment. Nevertheless, there remain several challenges to targeted therapies, including molecular identification, drug resistance, and exploring reliable biomarkers. Here, we present several selected signaling pathways and molecular targets involved in human cancers including Aurora kinases, PI3K/mTOR signaling, FOXO-FOXM1 axis, and MDM2/MDM4-p53 interaction. Understanding the molecular mechanisms for tumorigenesis and development of drug resistance will provide new insights into drug discovery and design of therapeutic strategies for targeted therapies.
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spelling pubmed-38456082013-12-11 Targeted therapy: tailoring cancer treatment Yan, Min Liu, Quentin Qiang Chin J Cancer Editorial Targeted therapies include small-molecule inhibitors and monoclonal antibodies, have made treatment more tumor-specific and less toxic, and have opened new possibilities for tailoring cancer treatment. Nevertheless, there remain several challenges to targeted therapies, including molecular identification, drug resistance, and exploring reliable biomarkers. Here, we present several selected signaling pathways and molecular targets involved in human cancers including Aurora kinases, PI3K/mTOR signaling, FOXO-FOXM1 axis, and MDM2/MDM4-p53 interaction. Understanding the molecular mechanisms for tumorigenesis and development of drug resistance will provide new insights into drug discovery and design of therapeutic strategies for targeted therapies. Sun Yat-sen University Cancer Center 2013-07 /pmc/articles/PMC3845608/ /pubmed/23823626 http://dx.doi.org/10.5732/cjc.013.10114 Text en Chinese Journal of Cancer http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Editorial
Yan, Min
Liu, Quentin Qiang
Targeted therapy: tailoring cancer treatment
title Targeted therapy: tailoring cancer treatment
title_full Targeted therapy: tailoring cancer treatment
title_fullStr Targeted therapy: tailoring cancer treatment
title_full_unstemmed Targeted therapy: tailoring cancer treatment
title_short Targeted therapy: tailoring cancer treatment
title_sort targeted therapy: tailoring cancer treatment
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845608/
https://www.ncbi.nlm.nih.gov/pubmed/23823626
http://dx.doi.org/10.5732/cjc.013.10114
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