Deconstructing breast cancer cell biology and the mechanisms of multidrug resistance

被引:78
|
作者
Videira, Mafalda [1 ,2 ]
Reis, Rita Leones [1 ]
Brito, Maria Alexandra [1 ,3 ]
机构
[1] Univ Lisbon, Fac Farm, Res Inst Med iMed ULisboa, P-1649003 Lisbon, Portugal
[2] Univ Lisbon, Fac Farm, Dept Galen Pharm & Pharmaceut Technol, P-1649003 Lisbon, Portugal
[3] Univ Lisbon, Fac Farm, Dept Biochem & Human Biol, P-1649003 Lisbon, Portugal
来源
关键词
Cancer biology; Chemoresistance; Efflux transporters; Epithelial-mesenchymal transition; Multidrug resistance proteins; Tumor microenvironment; TO-MESENCHYMAL TRANSITION; ENDOTHELIAL GROWTH-FACTOR; HYPOXIA-INDUCIBLE FACTOR-1; P-GLYCOPROTEIN INHIBITOR; IN-VIVO REVERSAL; FACTOR-KAPPA-B; DRUG-RESISTANCE; STEM-CELLS; PROTEIN BCRP/ABCG2; PHOSPHATIDYLINOSITOL; 3-KINASE;
D O I
10.1016/j.bbcan.2014.07.011
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
Cancer complexity constantly challenges the way that clinicians manage breast cancer therapy. Tumor heterogeneity and intratumoral stroma characteristics allow cells with different phenotypes and deregulated apoptotic, proliferative and migration abilities to co-exist contributing to a disappointing therapeutic response. While new approaches are being associated with conventional chemotherapy, such as hormonal therapy or target monoclonal antibodies, recurrence and metastasization are still observed. Membrane transporters are the cell's first line of contact with anticancer drugs having a major role in multidrug resistance events. This structural-based activity enables the cell to be drug-resistant by decreasing drug intracellular concentration through an efflux-transport mechanism, mainly associated with overexpression of ATP-binding cassette (ABC) proteins. This review focuses on some of the important structural and biological properties of the malignant cell and tumor microenvironment, addressing the role of the membrane ABC transporters in therapeutic outcomes, and highlighting related molecular pathways that may represent meaningful target therapies. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:312 / 325
页数:14
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