Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Abu Samaan, Tala M., Samec, Marek, Liskova, Alena, Kubatka, Peter, Büsselberg, Dietrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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
_version_ 1783493400950996992
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
work_keys_str_mv AT abusamaantalam paclitaxelsmechanisticandclinicaleffectsonbreastcancer
AT samecmarek paclitaxelsmechanisticandclinicaleffectsonbreastcancer
AT liskovaalena paclitaxelsmechanisticandclinicaleffectsonbreastcancer
AT kubatkapeter paclitaxelsmechanisticandclinicaleffectsonbreastcancer
AT busselbergdietrich paclitaxelsmechanisticandclinicaleffectsonbreastcancer