1. Identification of Oral Bioavailable Coumarin Derivatives as Potential AR Antagonists Targeting Prostate Cancer.
- Author
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Liao J, Liao J, Zhang M, Yu Y, Cai L, Le K, Fu W, Qin Y, Hou T, Li D, and Sheng R
- Subjects
- Male, Humans, Animals, Administration, Oral, Mice, Structure-Activity Relationship, Cell Line, Tumor, Antineoplastic Agents pharmacology, Antineoplastic Agents chemistry, Antineoplastic Agents pharmacokinetics, Antineoplastic Agents therapeutic use, Mice, Nude, Xenograft Model Antitumor Assays, Cell Proliferation drug effects, Coumarins chemistry, Coumarins pharmacology, Coumarins pharmacokinetics, Prostatic Neoplasms drug therapy, Prostatic Neoplasms pathology, Androgen Receptor Antagonists pharmacology, Androgen Receptor Antagonists chemistry, Androgen Receptor Antagonists pharmacokinetics, Androgen Receptor Antagonists therapeutic use, Androgen Receptor Antagonists chemical synthesis, Receptors, Androgen metabolism, Biological Availability
- Abstract
Androgen receptor (AR) is a crucial driver of prostate cancer (PCa), but acquired resistance to AR antagonists significantly undermines their clinical efficacy. We previously discovered coumarin derivative 1 , which is capable of disrupting AR ligand-binding domain dimers, offering the potential for overcoming resistance. However, its poor oral bioavailability limited further development. In this study, comprehensive structure optimizations led to compound 4a (IC
50 = 0.051 μM), which exhibited comparable AR antagonistic activity to enzalutamide (IC50 = 0.060 μM) and demonstrated excellent selectivity over other nuclear receptors in vitro. Especially, 4a showed superior efficacy against ARF876L/T877A and ARW741C mutants compared to darolutamide and enzalutamide. Moreover, 4a exhibited favorable pharmacokinetic profiles ( F = 66.24%) in vivo and significant tumor growth inhibition in an LNCaP xenograft mouse model upon oral administration. These results highlight the potential of 4a as a promising oral AR antagonist for overcoming drug resistance in PCa.- Published
- 2024
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