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Paclitaxel’s Mechanistic and Clinical Effects on Breast Cancer
Paclitaxel (PTX), the most widely used anticancer drug, is applied for the treatment of various types of malignant diseases. Mechanisms of PTX action represent several ways in which PTX affects cellular processes resulting in programmed cell death. PTX is frequently used as the first-line treatment...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995578/ https://www.ncbi.nlm.nih.gov/pubmed/31783552 http://dx.doi.org/10.3390/biom9120789 |
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author | Abu Samaan, Tala M. Samec, Marek Liskova, Alena Kubatka, Peter Büsselberg, Dietrich |
author_facet | Abu Samaan, Tala M. Samec, Marek Liskova, Alena Kubatka, Peter Büsselberg, Dietrich |
author_sort | Abu Samaan, Tala M. |
collection | PubMed |
description | Paclitaxel (PTX), the most widely used anticancer drug, is applied for the treatment of various types of malignant diseases. Mechanisms of PTX action represent several ways in which PTX affects cellular processes resulting in programmed cell death. PTX is frequently used as the first-line treatment drug in breast cancer (BC). Unfortunately, the resistance of BC to PTX treatment is a great obstacle in clinical applications and one of the major causes of death associated with treatment failure. Factors contributing to PTX resistance, such as ABC transporters, microRNAs (miRNAs), or mutations in certain genes, along with side effects of PTX including peripheral neuropathy or hypersensitivity associated with the vehicle used to overcome its poor solubility, are responsible for intensive research concerning the use of PTX in preclinical and clinical studies. Novelties such as albumin-bound PTX (nab-PTX) demonstrate a progressive approach leading to higher efficiency and decreased risk of side effects after drug administration. Moreover, PTX nanoparticles for targeted treatment of BC promise a stable and efficient therapeutic intervention. Here, we summarize current research focused on PTX, its evaluations in preclinical research and application clinical practice as well as the perspective of the drug for future implication in BC therapy. |
format | Online Article Text |
id | pubmed-6995578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69955782020-02-13 Paclitaxel’s Mechanistic and Clinical Effects on Breast Cancer Abu Samaan, Tala M. Samec, Marek Liskova, Alena Kubatka, Peter Büsselberg, Dietrich Biomolecules Review Paclitaxel (PTX), the most widely used anticancer drug, is applied for the treatment of various types of malignant diseases. Mechanisms of PTX action represent several ways in which PTX affects cellular processes resulting in programmed cell death. PTX is frequently used as the first-line treatment drug in breast cancer (BC). Unfortunately, the resistance of BC to PTX treatment is a great obstacle in clinical applications and one of the major causes of death associated with treatment failure. Factors contributing to PTX resistance, such as ABC transporters, microRNAs (miRNAs), or mutations in certain genes, along with side effects of PTX including peripheral neuropathy or hypersensitivity associated with the vehicle used to overcome its poor solubility, are responsible for intensive research concerning the use of PTX in preclinical and clinical studies. Novelties such as albumin-bound PTX (nab-PTX) demonstrate a progressive approach leading to higher efficiency and decreased risk of side effects after drug administration. Moreover, PTX nanoparticles for targeted treatment of BC promise a stable and efficient therapeutic intervention. Here, we summarize current research focused on PTX, its evaluations in preclinical research and application clinical practice as well as the perspective of the drug for future implication in BC therapy. MDPI 2019-11-27 /pmc/articles/PMC6995578/ /pubmed/31783552 http://dx.doi.org/10.3390/biom9120789 Text en © 2019 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 Abu Samaan, Tala M. Samec, Marek Liskova, Alena Kubatka, Peter Büsselberg, Dietrich Paclitaxel’s Mechanistic and Clinical Effects on Breast Cancer |
title | Paclitaxel’s Mechanistic and Clinical Effects on Breast Cancer |
title_full | Paclitaxel’s Mechanistic and Clinical Effects on Breast Cancer |
title_fullStr | Paclitaxel’s Mechanistic and Clinical Effects on Breast Cancer |
title_full_unstemmed | Paclitaxel’s Mechanistic and Clinical Effects on Breast Cancer |
title_short | Paclitaxel’s Mechanistic and Clinical Effects on Breast Cancer |
title_sort | paclitaxel’s mechanistic and clinical effects on breast cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995578/ https://www.ncbi.nlm.nih.gov/pubmed/31783552 http://dx.doi.org/10.3390/biom9120789 |
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