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Subunits of BK channels promote breast cancer development and modulate responses to endocrine treatment in preclinical models
British Journal of Pharmacology ( IF 6.8 ) Pub Date : 2020-05-28 , DOI: 10.1111/bph.15147
Corinna J Mohr 1, 2 , Werner Schroth 2 , Thomas E Mürdter 2 , Dominic Gross 1 , Selina Maier 1, 2 , Benjamin Stegen 3 , Alice Dragoi 1 , Friederike A Steudel 1 , Severine Stehling 1 , Reiner Hoppe 2 , Stephen Madden 4 , Peter Ruth 1 , Stephan M Huber 3 , Hiltrud Brauch 2, 5, 6 , Robert Lukowski 1
Affiliation  

Pore-forming α subunits of the voltage- and Ca2+-activated K+ channel with large conductance (BKα) promote malignant phenotypes of breast tumour cells. Auxiliary subunits such as the leucine-rich repeat containing 26 (LRRC26) protein, also termed BKγ1, may be required to permit activation of BK currents at a depolarized resting membrane potential that frequently occur in non-excitable tumour cells.

中文翻译:

在临床前模型中,BK 通道的亚基促进乳腺癌的发展并调节对内分泌治疗的反应

具有大电导(BKα)的电压和Ca 2+激活的K +通道的成孔α亚基促进乳腺肿瘤细胞的恶性表型。可能需要辅助亚基,例如富含亮氨酸的重复序列 26 (LRRC26) 蛋白,也称为 BKγ1,以允许在去极化的静息膜电位下激活 BK 电流,这种电位经常发生在不可兴奋的肿瘤细胞中。
更新日期:2020-05-28
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