Novel Potent ABCB1 Modulator, Phenethylisoquinoline Alkaloid, Reverses Multidrug Resistance in Cancer Cell
Norihiko Sugisawa1, Shinobu Ohnuma1, Hirofumi Ueda2
1Department of Surgery , Tohoku University Graduate School of Medicine , Sendai 980-8574 , Japan.
Abstract:
ATP-binding cassette (ABC) transporters, which are concerned with the efflux of anticancer drugs from cancer cells, have a pivotal role in multidrug resistance (MDR). In particular, ABCB1 is a well-known ABC transporter that develops MDR in many cancer cells. Some ABCB1 modulators can reverse ABCB1-mediated MDR; however, no modulators with clinical efficacy have been approved. The aim of this study was to identify novel ABCB1 modulators by using high-throughput screening. Of the 5861 compounds stored at Tohoku University, 13 compounds were selected after the primary screening via a fluorescent plate reader-based calcein acetoxymethylester (AM) efflux assay. These 13 compounds were validated in a flow cytometry-based calcein AM efflux assay. Two isoquinoline derivatives were identified as novel ABCB1 inhibitors, one of which was a phenethylisoquinoline alkaloid, (±)-7-benzyloxy-1-(3-benzyloxy-4-methoxyphenethyl)-1,2,3,4-tetrahydro-6-methoxy-2-methylisoquinoline oxalate. The compound, a phenethylisoquinoline alkaloid, was subsequently evaluated in the cytotoxicity assay and shown to significantly enhance the reversal of ABCB1-mediated MDR. In addition, the compound activated the ABCB1-mediated ATP hydrolysis and inhibited the photolabeling of ABCB1 with [125I]-iodoarylazidoprazosin. Furthermore, the compound also reversed the resistance to paclitaxel without increasing the toxicity in the ABCB1-overexpressing KB-V1 cell xenograft model. Overall, we concluded that the newly identified phenethylisoquinoline alkaloid reversed ABCB1-mediated MDR through direct interaction with the substrate-binding site of ABCB1. These findings may contribute to the development of more potent and less toxic ABCB1 modulators, which could overcome ABCB1-mediated MDR.
Insights
Researchers identified a novel phenethylisoquinoline alkaloid that reverses multidrug resistance (MDR) by directly inhibiting ATP-binding cassette subfamily B member 1 (ABCB1) transporters. This compound shows potential for developing new cancer therapies with reduced toxicity.
Area of Science:
- Pharmacology
- Molecular Biology
- Oncology
Background:
- ATP-binding cassette (ABC) transporters, particularly ABCB1, are crucial in mediating multidrug resistance (MDR) by exporting anticancer drugs from cancer cells.
- Existing ABCB1 modulators lack clinical efficacy, necessitating the discovery of novel compounds to overcome MDR.
Purpose of the Study:
- To identify novel modulators of ABCB1 using high-throughput screening.
- To characterize the mechanism of action of identified ABCB1 inhibitors.
Main Methods:
- High-throughput screening of 5861 compounds using calcein AM efflux assays (fluorescent plate reader and flow cytometry).
- Evaluation of identified inhibitors in cytotoxicity assays, ATP hydrolysis assays, and photolabeling assays.
- Assessment of a lead compound in an ABCB1-overexpressing KB-V1 cell xenograft model.
Main Results:
- Two isoquinoline derivatives were identified as novel ABCB1 inhibitors, with one phenethylisoquinoline alkaloid showing significant MDR reversal.
- The identified alkaloid activated ABCB1-mediated ATP hydrolysis, inhibited photolabeling, and reversed paclitaxel resistance without increasing toxicity in vivo.
Conclusions:
- The novel phenethylisoquinoline alkaloid directly interacts with the ABCB1 substrate-binding site, effectively reversing ABCB1-mediated MDR.
- These findings offer a promising foundation for developing potent and less toxic ABCB1 modulators to combat multidrug resistance in cancer therapy.
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