Understanding Breast cancer: from conventional therapies to repurposed drugs

被引:65
作者
Costa, Barbara [1 ]
Amorim, Irina [2 ,3 ,4 ]
Gartner, Fatima [2 ,3 ,4 ]
Vale, Nuno [1 ,2 ,3 ,4 ]
机构
[1] Univ Porto, Fac Pharm, Dept Drug Sci, Lab Pharmacol, Rua Jorge Viterbo 228, P-4050313 Porto, Portugal
[2] Univ Porto, Dept Mol Pathol & Immunol, Inst Biomed Sci Abel Salazar ICBAS, Rua Jorge Viterbo 228, Porto, Portugal
[3] Univ Porto IPATIMUP, Inst Mol Pathol & Immunol, Rua Julio Amaral Carvalho 45, P-4200135 Porto, Portugal
[4] Univ Porto, I3S, Inst Invest & Inovacao Saude, Rua Alfredo Allen, P-4200135 Porto, Portugal
关键词
Breast cancer; Drug repurposing; Drug combination; Drug resistance; ATRIAL-NATRIURETIC-PEPTIDE; INHIBITS TUMOR-GROWTH; STEM-LIKE PROPERTIES; CELL-GROWTH; ANTITUMOR-ACTIVITY; ESTROGEN-RECEPTOR; MEGESTROL-ACETATE; ENDOCRINE THERAPY; PROSTATE-CANCER; IN-VITRO;
D O I
10.1016/j.ejps.2020.105401
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Breast cancer is the most common cancer among women and is considered a developed country disease. Moreover, is a heterogenous disease, existing di fferent types and stages of breast cancer development, therefore, better understanding of cancer biology, helps to improve the development of therapies. The conventional treatments accessible after diagnosis, have the main goal of controlling the disease, by improving survival. In more advance stages the aim is to prolong life and symptom palliation care. Surgery, radiation therapy and chemotherapy are the main options available, which must be adapted to each person individually. However, patients are developing resistance to the conventional therapies. This resistance is due to alterations in important regulatory pathways such as PI3K/AKt/mTOR, this pathway contributes to trastuzumab resistance, a reference drug to treat breast cancer. Therefore, is proposed the repurposing of drugs, instead of developing drugs de novo, for example, to seek new medical treatments within the drugs available, to be used in breast cancer treatment. Providing safe and tol- erable treatments to patients, and new insights to e fficacy and e fficiency of breast cancer treatments. The economic and social burden of cancer is enormous so it must be taken measures to relieve this burden and to ensure continued access to therapies to all patients. In this review we focus on how conventional therapies against breast cancer are leading to resistance, by reviewing those mechanisms and discussing the e fficacy of repurposed drugs to fight breast cancer.
引用
收藏
页数:26
相关论文
共 333 条
[1]   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
[2]   Sirolimus and trastuzumab combination therapy for HER2-positive metastatic breast cancer after progression on prior trastuzumab therapy [J].
Acevedo-Gadea, Carlos ;
Hatzis, Christos ;
Chung, Gina ;
Fishbach, Neal ;
Lezon-Geyda, Kimberly ;
Zelterman, Daniel ;
DiGiovanna, Michael P. ;
Harris, Lyndsay ;
Abu-Khalaf, Maysa M. .
BREAST CANCER RESEARCH AND TREATMENT, 2015, 150 (01) :157-167
[3]   Anti-inflammatory agent indomethacin reduces invasion and alters metabolism in a human breast cancer cell line [J].
Ackerstaff, Ellen ;
Gimi, Barjor ;
Artemov, Dmitri ;
Bhujwalla, Zaver M. .
NEOPLASIA, 2007, 9 (03) :222-235
[4]   Awareness and current knowledge of breast cancer [J].
Akram, Muhammad ;
Iqbal, Mehwish ;
Daniyal, Muhammad ;
Khan, Asmat Ullah .
BIOLOGICAL RESEARCH, 2017, 50
[5]  
Alaee M, 2017, J BREAST CANCER, V20, P20
[6]   Breast cancer risk by age at birth, time since birth and time intervals between births:: exploring interaction effects [J].
Albrektsen, G ;
Heuch, I ;
Hansen, S ;
Kvåle, G .
BRITISH JOURNAL OF CANCER, 2005, 92 (01) :167-175
[7]   Inhibition of the CCL5/CCR5 Axis against the Progression of Gastric Cancer [J].
Aldinucci, Donatella ;
Casagrande, Naike .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (05)
[8]  
Aleck K, 2017, BIORESEARCH OPEN ACC, V6, P141, DOI 10.1089/biores.2017.0009
[9]  
ALKAN FU, 2012, THESCIENTIFICWORLDJO, DOI DOI 10.1100/2012/976740
[10]  
ALLEGRA JC, 1987, SEMIN HEMATOL, V24, P45