Experimental Models as Refined Translational Tools for Breast Cancer Research

被引:18
作者
Costa, Eduardo [1 ,2 ,3 ,4 ]
Ferreira-Goncalves, Tania [4 ]
Chasqueira, Goncalo [5 ]
Cabrita, Antonio S. [1 ]
Figueiredo, Isabel, V [2 ,6 ]
Reis, Catarina Pinto [4 ,7 ]
机构
[1] Univ Coimbra, Fac Med, Expt Pathol Serv, P-3000548 Coimbra, Portugal
[2] Univ Coimbra, Fac Pharm, Pharmacol & Pharmaceut Care Lab, P-3000548 Coimbra, Portugal
[3] Vasco da Gama Univ Sch EUVG, Vasco da Gama Res Grp CIVG, Av Jose R Sousa Fernandes,Campus Univ,Bloco B, P-3020210 Coimbra, Portugal
[4] Univ Lisbon, iMed ULisboa, Fac Farm, Av Prof Gama Pinto, P-1649003 Lisbon, Portugal
[5] Univ Lisbon, Fac Farm, Av Prof Gama Pinto, P-1649003 Lisbon, Portugal
[6] Univ Coimbra, Inst Clin & Biomed Res iCBR, Fac Med, P-3000548 Coimbra, Portugal
[7] Univ Lisbon, Fac Ciencias, IBEB, P-1749016 Lisbon, Portugal
关键词
oncology; breast cancer; experimental models; animal models; in vitro; in silico; pharmacological testing; strategies of drug development;
D O I
10.3390/scipharm88030032
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Breast cancer is one of the most common cancers worldwide, which makes it a very impactful malignancy in the society. Breast cancers can be classified through different systems based on the main tumor features and gene, protein, and cell receptors expression, which will determine the most advisable therapeutic course and expected outcomes. Multiple therapeutic options have already been proposed and implemented for breast cancer treatment. Nonetheless, their use and efficacy still greatly depend on the tumor classification, and treatments are commonly associated with invasiveness, pain, discomfort, severe side effects, and poor specificity. This has demanded an investment in the research of the mechanisms behind the disease progression, evolution, and associated risk factors, and on novel diagnostic and therapeutic techniques. However, advances in the understanding and assessment of breast cancer are dependent on the ability to mimic the properties and microenvironment of tumors in vivo, which can be achieved through experimentation on animal models. This review covers an overview of the main animal models used in breast cancer research, namely in vitro models, in vivo models, in silico models, and other models. For each model, the main characteristics, advantages, and challenges associated to their use are highlighted.
引用
收藏
页码:1 / 29
页数:29
相关论文
共 241 条
[41]   Animal models of breast cancer: Their diversity and role in biomedical research [J].
Clarke, R .
BREAST CANCER RESEARCH AND TREATMENT, 1996, 39 (01) :1-6
[42]   In silico modelling of physiologic systems [J].
Colquitt, Richard B. ;
Colquhoun, Douglas A. ;
Thiele, Robert H. .
BEST PRACTICE & RESEARCH-CLINICAL ANAESTHESIOLOGY, 2011, 25 (04) :499-510
[43]  
Conn PM, 2013, ANIMAL MODELS FOR THE STUDY OF HUMAN DISEASE, pXIII
[44]   3D tumor spheroids: an overview on the tools and techniques used for their analysis [J].
Costa, Elisabete C. ;
Moreira, Andre F. ;
de Melo-Diogo, Duarte ;
Gaspar, Vitor M. ;
Carvalho, Marco P. ;
Correia, Ilidio J. .
BIOTECHNOLOGY ADVANCES, 2016, 34 (08) :1427-1441
[45]   Characterizing a rat Brca2 knockout model [J].
Cotroneo, M. S. ;
Haag, J. D. ;
Zan, Y. ;
Lopez, C. C. ;
Thuwajit, P. ;
Petukhova, G. V. ;
Camerini-Otero, R. D. ;
Gendron-Fitzpatrick, A. ;
Griep, A. E. ;
Murphy, C. J. ;
Dubielzig, R. R. ;
Gould, M. N. .
ONCOGENE, 2007, 26 (11) :1626-1635
[46]  
Council of Europe, 1986, EUR TREAT SER, V123
[47]  
Cressman VL, 1999, CELL GROWTH DIFFER, V10, P1
[48]   Oncogenic signaling pathways activated in DMBA-induced mouse mammary tumors [J].
Currier, N ;
Solomon, SE ;
Demicco, EG ;
Chang, DLF ;
Farago, M ;
Ying, HQ ;
Dominguez, I ;
Sonenshein, GE ;
Cardiff, RD ;
Xiao, ZXJ ;
Sherr, DH ;
Seldin, DC .
TOXICOLOGIC PATHOLOGY, 2005, 33 (06) :726-737
[49]   Breast Cancer Cell Line Classification and Its Relevance with Breast Tumor Subtyping [J].
Dai, Xiaofeng ;
Cheng, Hongye ;
Bai, Zhonghu ;
Li, Jia .
JOURNAL OF CANCER, 2017, 8 (16) :3131-3141
[50]   Breast Cancer Cell Invasion into a Three Dimensional Tumor-Stroma Microenvironment [J].
Danh Truong ;
Puleo, Julieann ;
Llave, Alison ;
Mouneimne, Ghassan ;
Kamm, Roger D. ;
Nikkhah, Mehdi .
SCIENTIFIC REPORTS, 2016, 6