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Progress in targeted therapy for breast cancer

Breast cancer is a multistep, multifactorial, and heterogeneous disease. Significant transformations have occurred in the systemic management of breast cancer in the past decade. Due to the further understanding of pathogenesis, scientists have found plenty of signaling pathways and correspondingly...

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Detalles Bibliográficos
Autores principales: Ju, Jie, Zhu, An-Jie, Yuan, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Medical Association 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160667/
https://www.ncbi.nlm.nih.gov/pubmed/30276363
http://dx.doi.org/10.1016/j.cdtm.2018.04.002
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author Ju, Jie
Zhu, An-Jie
Yuan, Peng
author_facet Ju, Jie
Zhu, An-Jie
Yuan, Peng
author_sort Ju, Jie
collection PubMed
description Breast cancer is a multistep, multifactorial, and heterogeneous disease. Significant transformations have occurred in the systemic management of breast cancer in the past decade. Due to the further understanding of pathogenesis, scientists have found plenty of signaling pathways and correspondingly therapeutic targets in breast cancer, such as hormone receptor, human epidermal growth factor receptor 2 (HER2), epidermal growth factor receptor (EGFR), vascular endothelial growth factor (VEGF), phosphoinositide-3-kinase (PI3K), v-akt murine thymoma viral oncogene homolog (AKT), mechanistic target of rapamycin (mTOR), cyclin-dependent kinase 4/6 (CDK4/6), poly (adenosine diphosphate-ribose) polymerase (PARP), and programmed death-1 (PD-1). Targeted therapy, which optimizes the accuracy of antitumor activity and minimizes toxicity to normal tissues, plays a crucial role in breast cancer treatment in the era of precision medicine. In this review, we aimed to summarize the latest developments in targeted therapy for breast cancer and discuss the existing problems.
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spelling pubmed-61606672018-10-01 Progress in targeted therapy for breast cancer Ju, Jie Zhu, An-Jie Yuan, Peng Chronic Dis Transl Med Perspective Breast cancer is a multistep, multifactorial, and heterogeneous disease. Significant transformations have occurred in the systemic management of breast cancer in the past decade. Due to the further understanding of pathogenesis, scientists have found plenty of signaling pathways and correspondingly therapeutic targets in breast cancer, such as hormone receptor, human epidermal growth factor receptor 2 (HER2), epidermal growth factor receptor (EGFR), vascular endothelial growth factor (VEGF), phosphoinositide-3-kinase (PI3K), v-akt murine thymoma viral oncogene homolog (AKT), mechanistic target of rapamycin (mTOR), cyclin-dependent kinase 4/6 (CDK4/6), poly (adenosine diphosphate-ribose) polymerase (PARP), and programmed death-1 (PD-1). Targeted therapy, which optimizes the accuracy of antitumor activity and minimizes toxicity to normal tissues, plays a crucial role in breast cancer treatment in the era of precision medicine. In this review, we aimed to summarize the latest developments in targeted therapy for breast cancer and discuss the existing problems. Chinese Medical Association 2018-07-07 /pmc/articles/PMC6160667/ /pubmed/30276363 http://dx.doi.org/10.1016/j.cdtm.2018.04.002 Text en © 2018 Chinese Medical Association. Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Perspective
Ju, Jie
Zhu, An-Jie
Yuan, Peng
Progress in targeted therapy for breast cancer
title Progress in targeted therapy for breast cancer
title_full Progress in targeted therapy for breast cancer
title_fullStr Progress in targeted therapy for breast cancer
title_full_unstemmed Progress in targeted therapy for breast cancer
title_short Progress in targeted therapy for breast cancer
title_sort progress in targeted therapy for breast cancer
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160667/
https://www.ncbi.nlm.nih.gov/pubmed/30276363
http://dx.doi.org/10.1016/j.cdtm.2018.04.002
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