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The efficacy and mechanism of the novel small molecule degradation agent LS-13 targeting ARfl/ARv7 to inhibit enzalutamide resistant in prostate cancer
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Zheng-yi HAN1, Yan LIANG4, Peng CAO1, 2, Zhen-yu YIN3, *, Yan LI2, *
Acta Pharmaceutica Sinica | 2025, 60(6) : 1739 - 1745
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Acta Pharmaceutica Sinica | 2025, 60(6): 1739-1745
• Original Articles •
The efficacy and mechanism of the novel small molecule degradation agent LS-13 targeting ARfl/ARv7 to inhibit enzalutamide resistant in prostate cancer
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Zheng-yi HAN1, Yan LIANG4, Peng CAO1, 2, Zhen-yu YIN3, *, Yan LI2, *
Affiliations
  • 1School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China
  • 2National Key Laboratory of Process Control and Intelligent Manufacturing Technology for Traditional Chinese Medicine Pharmaceutical Production, Nanjing University of Chinese Medicine, Nanjing 210023, China
  • 3Gulou Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing 210008, China
  • 4Affiliated Jinling Hospital, Medical School of Nanjing University/General Hospital of Eastern Theater Command, Nanjing 210007, China
Published: 2025-06-12 doi: 10.16438/j.0513-4870.2025-0061
Outline
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Enzalutamide resistance (ENZR) is the most common issue in castration-resistant prostate cancer (CRPC). After a period of treatment with the second-generation androgen receptor (AR) inhibitor enzalutamide (ENZ), patients develop resistance to ENZ, posing a serious threat to male health. However, there are currently no effective drugs for treating prostate cancer patients with ENZ resistance. Based on the structural optimization and modification of enzalutamide, and through molecular biological methods such as cell viability assays, colony formation, cell apoptosis detection, Western blot and other molecular biology techniques, it was discovered that the half-maximal inhibitory concentration values of LS-13 for prostate cancer LNCaP-ENZR and 22RV1 cells are 17.09 and 19.90 μmol·L-1, respectively. Subsequently, after treating the resistant cell lines with 0.1, 1, 5, and 10 μmol·L-1 of LS-13 for 12 days, the observation results indicated that LS-13 could inhibit the in vitro clonal formation of LNCaP-ENZR and 22RV1 cells in a dose-dependent manner. Furthermore, after treating the resistant cell lines with 1.25, 2.5, 5, and 10 μmol·L-1 of LS-13 for 72 h, the results of flow cytometry also showed that LS-13 could promote apoptosis of the resistant cell lines in a dose-dependent manner. Furthermore, under the same concentration conditions described above, after LS-13 treatment of 22RV1 cells for 24 h, it was found that their migration speed was significantly slowed down (P < 0.05). These results collectively indicate that the small molecule compound LS-13 has a pronounced effect in inhibiting ENZR. Further mechanism studies found that LS-13 can target ARfl/ARv7 and promote its protein degradation, inhibit the transcription levels of AR-downstream target genes, thereby suppressing ENZR cell proliferation and promoting apoptosis. This study provides a candidate compound for targeting ARfl/ARv7 to overcome ENZ resistance.

prostate cancer  /  drug resistance  /  enzalutamide  /  degradation  /  androgen receptor
韩正义, 梁艳, 曹鹏, 尹震宇, 李岩. 靶向ARfl/ARv7新型小分子降解剂LS-13抑制前列腺癌恩杂鲁胺耐药的药效及机制研究. 药学学报, 2025 , 60 (6) : 1739 -1745 . DOI: 10.16438/j.0513-4870.2025-0061
Zheng-yi HAN, Yan LIANG, Peng CAO, Zhen-yu YIN, Yan LI. The efficacy and mechanism of the novel small molecule degradation agent LS-13 targeting ARfl/ARv7 to inhibit enzalutamide resistant in prostate cancer[J]. Acta Pharmaceutica Sinica, 2025 , 60 (6) : 1739 -1745 . DOI: 10.16438/j.0513-4870.2025-0061
Year 2025 volume 60 Issue 6
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Article Info
doi: 10.16438/j.0513-4870.2025-0061
  • Receive Date:2025-01-17
  • Online Date:2026-09-20
  • Published:2025-06-12
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History
  • Received:2025-01-17
  • Revised:2025-04-01
Affiliations
    1School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China
    2National Key Laboratory of Process Control and Intelligent Manufacturing Technology for Traditional Chinese Medicine Pharmaceutical Production, Nanjing University of Chinese Medicine, Nanjing 210023, China
    3Gulou Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing 210008, China
    4Affiliated Jinling Hospital, Medical School of Nanjing University/General Hospital of Eastern Theater Command, Nanjing 210007, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
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属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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