دورية أكاديمية

FRAX486, a PAK inhibitor, overcomes ABCB1-mediated multidrug resistance in breast cancer cells

التفاصيل البيبلوغرافية
العنوان: FRAX486, a PAK inhibitor, overcomes ABCB1-mediated multidrug resistance in breast cancer cells
المؤلفون: Meng Zhang, Xiaoqi Zeng, Meiling She, Xingduo Dong, Jun Chen, Qingquan Xiong, Guobin Qiu, Shuyi Yang, Xiangqi Li, Guanghui Ren
المصدر: Brazilian Journal of Medical and Biological Research, Vol 57 (2024)
بيانات النشر: Associação Brasileira de Divulgação Científica, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine (General)
LCC:Biology (General)
مصطلحات موضوعية: FRAX486, p21-activated kinase (PAK) inhibitor, Multidrug resistance, ABC transporter, ABCB1, Medicine (General), R5-920, Biology (General), QH301-705.5
الوصف: The overexpression of P-glycoprotein (P-gp/ABCB1) is a leading cause of multidrug resistance (MDR). Hence, it is crucial to discover effective pharmaceuticals that counteract ABCB1-mediated multidrug resistance. FRAX486 is a p21-activated kinase (PAK) inhibitor. The objective of this study was to investigate whether FRAX486 can reverse ABCB1-mediated multidrug resistance, while also exploring its mechanism of action. The CCK8 assay demonstrated that FRAX486 significantly reversed ABCB1-mediated multidrug resistance. Furthermore, western blotting and immunofluorescence experiments revealed that FRAX486 had no impact on expression level and intracellular localization of ABCB1. Notably, FRAX486 was found to enhance intracellular drug accumulation and reduce efflux, resulting in the reversal of multidrug resistance. Docking analysis also indicated a strong affinity between FRAX486 and ABCB1. This study highlights the ability of FRAX486 to reverse ABCB1-mediated multidrug resistance and provides valuable insights for its clinical application.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1414-431X
1414-431x
العلاقة: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2024000100654&lng=en&tlng=enTest; http://www.scielo.br/pdf/bjmbr/v57/1414-431X-bjmbr-57-e13357.pdfTest; https://doaj.org/toc/1414-431XTest
DOI: 10.1590/1414-431x2024e13357
الوصول الحر: https://doaj.org/article/2822698d56194bf1845e291b61ac846cTest
رقم الانضمام: edsdoj.2822698d56194bf1845e291b61ac846c
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1414431X
1414431x
DOI:10.1590/1414-431x2024e13357