Paclitaxel's Mechanistic and Clinical Effects on Breast Cancer

被引:439
作者
Abu Samaan, Tala M. [1 ]
Samec, Marek [2 ]
Liskova, Alena [2 ]
Kubatka, Peter [3 ]
Busselberg, Dietrich [4 ]
机构
[1] Qatar Fdn, Dept Premed Educ, Educ City, Weill Cornell Med Qatar, Doha 24144, Qatar
[2] Comenius Univ, Jessenius Fac Med, Clin Obstet & Gynecol, Martin 03601, Slovakia
[3] Comenius Univ, Jessenius Fac Med, Dept Med Biol, Martin 03601, Slovakia
[4] Qatar Fdn, Dept Physiol & Biophys, Educ City, Weill Cornell Med Qatar, Doha 24144, Qatar
关键词
breast cancer; anti-cancer therapy; chemotherapy; Paclitaxel; nanomedicine; phytochemicals; ALBUMIN-BOUND-PACLITAXEL; PHASE-II TRIAL; TAXOL-INDUCED APOPTOSIS; NAB-PACLITAXEL; CELL-LINES; BCL-2; PHOSPHORYLATION; INHIBITS PROGRESSION; POLYMERIC MICELLE; CARCINOMA CELLS; UP-REGULATION;
D O I
10.3390/biom9120789
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:22
相关论文
共 164 条
[1]   Taxane benefit in breast cancer-a role for grade and chromosomal stability [J].
A'Hern, Roger P. ;
Jamal-Hanjani, Mariam ;
Szasz, A. Marcell ;
Johnston, Stephen R. D. ;
Reis-Filho, Jorge S. ;
Roylance, Rebecca ;
Swanton, Charles .
NATURE REVIEWS CLINICAL ONCOLOGY, 2013, 10 (06) :357-364
[2]   Molecular basis for the development of novel taxanes in the treatment of metastatic breast cancer [J].
Aapro, Matti S. ;
Von Minckwitz, Gunter .
EJC SUPPLEMENTS, 2008, 6 (10) :3-11
[3]   Chemotherapeutic agents for the treatment of metastatic breast cancer: An update [J].
Abotaleb, Mariam ;
Kubatka, Peter ;
Caprnda, Martin ;
Varghese, Elizabeth ;
Zolakova, Barbora ;
Zubor, Pavol ;
Opatrilova, Radka ;
Kruzliak, Peter ;
Stefanicka, Patrik ;
Busselberg, Dietrich .
BIOMEDICINE & PHARMACOTHERAPY, 2018, 101 :458-477
[4]   Genetics of triple-negative breast cancer: Implications for patient care [J].
Afghahi, Anosheh ;
Telli, Melinda L. ;
Kurian, Allison W. .
CURRENT PROBLEMS IN CANCER, 2016, 40 (2-4) :130-140
[5]   THE PRODUCT OF THE HUMAN C-ERBB-2 GENE - A 185-KILODALTON GLYCOPROTEIN WITH TYROSINE KINASE-ACTIVITY [J].
AKIYAMA, T ;
SUDO, C ;
OGAWARA, H ;
TOYOSHIMA, K ;
YAMAMOTO, T .
SCIENCE, 1986, 232 (4758) :1644-1646
[6]   Differential altered expression of let-7a and miR-205 tumor-suppressor miRNAs in different subtypes of breast cancer under treatment with Taxol [J].
Asghari, Faezeh ;
Haghnavaz, Navideh ;
Shanehbandi, Darioush ;
Khaze, Vahid ;
Baradaran, Behzad ;
Kazemi, Tohid .
ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE, 2018, 27 (07) :941-945
[7]   Immunotherapy for HER2-positive breast cancer: recent advances and combination therapeutic approaches [J].
Ayoub, Nehad M. ;
Al-Shami, Kamal M. ;
Yaghan, Rami J. .
BREAST CANCER-TARGETS AND THERAPY, 2019, 11 :53-69
[8]   A multifunctional lipid nanoparticle for co-delivery of paclitaxel and curcumin for targeted delivery and enhanced cytotoxicity in multidrug resistant breast cancer cells [J].
Baek, Jong-Suep ;
Cho, Cheong-Weon .
ONCOTARGET, 2017, 8 (18) :30369-30382
[9]  
Baselga J, 1997, Oncology (Williston Park), V11, P43
[10]   Disparate Response to Methotrexate in Stem Versus Non-Stem Cells [J].
Beane, Olivia S. ;
Darling, Louise E. O. ;
Fonseca, Vera C. ;
Darling, Eric M. .
STEM CELL REVIEWS AND REPORTS, 2016, 12 (03) :340-351