Nakamura Natsuki, Miyamoto Takumi, Sanada Megumi, Nakamura Motonao
Department of Bioscience, Graduate School of Life Science, Okayama University of Science, 1-1 Ridai-cho, Kita-ku, Okayama, 700-0005, Japan.
Sci Rep. 2025 Jul 28;15(1):27451. doi: 10.1038/s41598-025-12889-5.
Anticancer drug resistance is a significant obstacle in chemotherapy. Although ABCB1, an ABC transporter, confers chemoresistance owing to the extrusion of drugs out of cells, ABCB1 blockers have not been developed. Here, we clarified the chemosensory role of bitter taste receptors (TAS2Rs) in response to incorporated drugs. The underlying mechanisms by which ABCB1 is regulated in cancer cells involve TAS2Rs, the activation of which triggers drug excretion by ABCB1. In MCF-7 cells, intracellular TAS2Rs were activated by incorporated substances, which elicited the Gα12/13/RhoA/ROCK/p38MAPK/NF-κB pathway, leading to ABCB1 upregulation. We validated that prolonged exposure of MCF-7 cells to TAS2R ligands helps defend against harmful compounds. These cells exhibit rapid excretion of substances and predominant growth in the presence of toxic drugs. This predominance disappeared after treatment with verapamil, an ABCB1 blocker, suggesting the involvement of ABCB1. We further determined that TAS2R14, one of TAS2Rs, is a receptor for doxorubicin, an anticancer drug. In MCF-7 cells, TAS2R14-deficiency diminished doxorubicin-induced ABCB1 production, resulting in higher sensitivity to doxorubicin than in control cells. Altogether, intracellular TAS2Rs act as gatekeepers that drive drug excretion. Blockers for TAS2R14 could be used as efficacious agents to attenuate the excretion of doxorubicin, resulting in escape from doxorubicin resistance.
抗癌药物耐药性是化疗中的一个重大障碍。尽管ABC转运蛋白ABCB1由于将药物排出细胞而导致化疗耐药,但ABCB1阻滞剂尚未研发出来。在此,我们阐明了苦味受体(TAS2Rs)对摄入药物的化学感应作用。癌细胞中ABCB1受调控的潜在机制涉及TAS2Rs,其激活会触发ABCB1介导的药物排泄。在MCF - 7细胞中,摄入的物质激活了细胞内的TAS2Rs,引发了Gα12/13/RhoA/ROCK/p38MAPK/NF - κB信号通路,导致ABCB1上调。我们证实,MCF - 7细胞长时间暴露于TAS2R配体有助于抵御有害化合物。这些细胞在有毒药物存在的情况下表现出物质的快速排泄和优势生长。在用ABCB1阻滞剂维拉帕米处理后,这种优势消失,表明ABCB1参与其中。我们进一步确定,TAS2Rs之一的TAS2R14是抗癌药物阿霉素的受体。在MCF - 7细胞中,TAS2R14缺陷减少了阿霉素诱导的ABCB1产生,导致其对阿霉素的敏感性高于对照细胞。总之,细胞内的TAS2Rs充当驱动药物排泄的守门人。TAS2R14阻滞剂可作为有效的药物来减少阿霉素的排泄,从而克服阿霉素耐药性。