Reverse Translational Research of ABCG2 (BCRP) in Human Disease and Drug Response

被引:27
作者
Brackman, Deanna J. [1 ]
Giacomini, Kathleen M. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA
关键词
CANCER RESISTANCE PROTEIN; CELL LUNG-CANCER; BREAST-CANCER; MULTIDRUG-RESISTANCE; ROSUVASTATIN PHARMACOKINETICS; GENETIC POLYMORPHISMS; ALZHEIMERS-DISEASE; TRANSPORTER ABCG2; RISK-FACTORS; PHASE-II;
D O I
10.1002/cpt.903
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Reverse translational research takes a bedside-to-bench approach, using sophisticated basic research to explain the biological mechanisms behind observed clinical data. For transporters, which play a role in human disease and drug response, this approach offers a distinct advantage over the typical translational research, which often falters due to inadequate in vitro and preclinical animal models. Research on ABCG2, which encodes the Breast Cancer Resistance Protein, has benefited immensely from a reverse translational approach due to its broad implications for disease susceptibility and both therapeutic and adverse drug response. In this review, we describe the success of reverse translational research for ABCG2 and opportunities for further studies.
引用
收藏
页码:233 / 242
页数:10
相关论文
共 50 条
  • [41] A role for ABCG2 beyond drug transport: Regulation of autophagy
    Ding, Rui
    Jin, Shengkan
    Pabon, Kirk
    Scotto, Kathleen W.
    AUTOPHAGY, 2016, 12 (05) : 737 - 751
  • [42] Efavirenz is a substrate and in turn modulates the expression of the efflux transporter ABCG2/BCRP in the gastrointestinal tract of the rat
    Peroni, Roxana N.
    Di Gennaro, Stefania S.
    Hocht, Christian
    Chiappetta, Diego A.
    Rubio, Modesto C.
    Sosnik, Alejandro
    Bramuglia, Guillermo F.
    BIOCHEMICAL PHARMACOLOGY, 2011, 82 (09) : 1227 - 1233
  • [43] Transmembrane helices 1 and 6 of the human breast cancer resistance protein (BCRP/ABCG2): identification of polar residues important for drug transport
    Ni, Zhanglin
    Bikadi, Zsolt
    Cai, Xiaokun
    Rosenberg, Mark F.
    Mao, Qingcheng
    AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2010, 299 (05): : C1100 - C1109
  • [44] Development and Validation of a Computational Model Ensemble for the Early Detection of BCRP/ABCG2 Substrates during the Drug Design Stage
    Gantner, Melisa E.
    Peroni, Roxana N.
    Morales, Juan F.
    Villalba, Maria L.
    Ruiz, Maria E.
    Talevi, Alan
    JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2017, 57 (08) : 1868 - 1880
  • [45] The phytoestrogens daidzein and equol inhibit the drug transporter BCRP/ABCG2 in breast cancer cells: potential chemosensitizing effect
    Juan Pablo Rigalli
    Paul Niklas Scholz
    Guillermo Nicolás Tocchetti
    María Laura Ruiz
    Johanna Weiss
    European Journal of Nutrition, 2019, 58 : 139 - 150
  • [46] Placental BCRP/ABCG2 Transporter Prevents Fetal Exposure to the Estrogenic Mycotoxin Zearalenone
    Szilagyi, John T.
    Gorczyca, Ludwik
    Brinker, Anita
    Buckley, Brian
    Laskin, Jeffrey D.
    Aleksunes, Lauren M.
    TOXICOLOGICAL SCIENCES, 2019, 168 (02) : 394 - 404
  • [47] Oleic acid increases intestinal absorption of the BCRP/ABCG2 substrate, mitoxantrone, in mice
    Aspenstrom-Fagerlund, Bitte
    Tallkvist, Jonas
    Ilback, Nils-Gunnar
    Glynn, Anders W.
    TOXICOLOGY LETTERS, 2015, 237 (02) : 133 - 139
  • [48] In Silico Prediction of Inhibition of Promiscuous Breast Cancer Resistance Protein (BCRP/ABCG2)
    Ding, Yi-Lung
    Shih, Yu-Hsuan
    Tsai, Fu-Yuan
    Leong, Max K.
    PLOS ONE, 2014, 9 (03):
  • [49] Effect of ABCG2/BCRP Expression on Efflux and Uptake of Gefitinib in NSCLC Cell Lines
    Galetti, Maricla
    Petronini, Pier Giorgio
    Fumarola, Claudia
    Cretella, Daniele
    La Monica, Silvia
    Bonelli, Mara
    Cavazzoni, Andrea
    Saccani, Francesca
    Caffarra, Cristina
    Andreoli, Roberta
    Mutti, Antonio
    Tiseo, Marcello
    Ardizzoni, Andrea
    Alfieri, Roberta R.
    PLOS ONE, 2015, 10 (11):
  • [50] Secretion into Milk of the Main Metabolites of the Anthelmintic Albendazole Is Mediated by the ABCG2/BCRP Transporter
    Blanco-Paniagua, Esther
    Alvarez-Fernandez, Laura
    Garcia-Lino, Alba M.
    Alvarez, Ana, I
    Merino, Gracia
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2022, 66 (07)