基础医学与临床 ›› 2026, Vol. 46 ›› Issue (1): 39-45.doi: 10.16352/j.issn.1001-6325.2026.01.0039

• 研究论文 • 上一篇    下一篇

小檗碱增强前列腺癌细胞系22RV1对多西他赛的化疗敏感性

陆巍1*, 王焱旻1, 刘炳辰1, 陶欣1, 王世鹏1, 曹秋也2   

  1. 1.吉林省人民医院 泌尿外科,吉林 长春 130021;
    2.乾安县人民医院 胸外泌尿科,吉林 松原 131499
  • 收稿日期:2025-01-07 修回日期:2025-04-28 出版日期:2026-01-05 发布日期:2025-12-29
  • 通讯作者: *wkkki2@163.com
  • 基金资助:
    吉林省卫生健康科技能力提升项目(2021JC055)

Berberine enhances the chemotherapy sensitivity of prostate cancer cell line 22RV1 to docetaxel

LU Wei1*, WANG Yanmin1, LIU Bingchen1, TAO Xin1, WANG Shipeng1, CAO Qiuye2   

  1. 1. Department of Urology, Jilin Provincial People's Hospital, Changchun 130021;
    2. Department of Thoracic and Urology, Qian'an County People's Hospital, Songyuan 131499, China
  • Received:2025-01-07 Revised:2025-04-28 Online:2026-01-05 Published:2025-12-29
  • Contact: *wkkki2@163.com

摘要: 目的 探讨小檗碱(BBR)增强前列腺癌细胞系22RV1对多西他赛(DTX)化学治疗(化疗)敏感性的影响。方法 利用前列腺癌细胞系22RV1细胞构建相应的DTX耐药细胞。将成功建立的耐药细胞株(22RV1/DTX)分为:22RV1/DTX组、低浓度(L)-BBR+22RV1/DTX组、高浓度(H)-BBR+22RV1/DTX组、H-BBR+ERK激活剂+22RV1/DTX组;CCK8法检测细胞增殖;划痕愈合试验检测迁移;Transwell小室法检测侵袭;流式细胞测量术检测凋亡;Western blot检测细胞中细胞外调节蛋白激酶(ERK)、pERK、ETS转录因子(ELK1)蛋白表达。结果 与22RV1/DTX组相比,L-BBR+22RV1/DTX组和H-BBR+22RV1/DTX组细胞的增殖、迁移、侵袭能力降低,凋亡率提高(P<0.05);与H-BBR+22RV1/DTX组相比,H-BBR+ERK激活剂+22RV1/DTX组细胞的增殖、迁移、侵袭能力提高,凋亡率降低(P<0.05);BBR可显著降低22RV1/DTX细胞pERK/ERK比值和ELK1的蛋白表达水平(P<0.05),且其对22RV1/DTX细胞及通路的影响可被ERK激活剂逆转(P<0.05)。结论 BBR可能通过抑制ERK/ELK1信号通路,抑制耐药细胞增殖、迁移、侵袭,促进细胞凋亡,增强前列腺癌细胞对DTX的化疗敏感性。

关键词: 小檗碱, ERK/ELK1, 前列腺癌细胞, 化疗敏感性

Abstract: Objective To investigate the chemotherapy effectiveness of berberine (BBR) to enhance sensitivity of prostate cancer cell line 22RV1 to docetaxel. Methods The docetaxel (DTX) resistant cell was constructed using prostate cancer cell line 22RV1. The drug-resistant cell strain(22RV1/DTX) was divided into: 22RV1/DTX group, low concentration (L)-BBB+22RV1/DTX group, high concentration (H)-BBB+22RV1/DTX group and H-BBR+ERK activator+22RV1/DTX group. CCK8 method was applied to detect cell proliferation. Scratch healing test was applied to detect migration. Transwell test was applied to detect invasion. Flow cytometry was applied to detect apoptosis. Western blot was applied to detect the expression of extra-cellular regulated protein kinases (ERK), pERK, and ETS transcription factor (ELK1) proteins in cells. Results Compared with 22RV1/DTX group, the proliferation, migration, and invasion of cells in the L-BBR+22RV1/DTX group and H-BBR+22RV1/DTX group were lower but the apoptosis rate was higher (P<0.05). The proliferation, migration, and invasion of cells in the H-BBR+ERK activator+22RV1/DTX group were higher, and the apoptosis rate was lower (P<0.05). BBR significantly reduced the pERK/ERK ratio and ELK1 protein expression level in 22RV1/DTX cells(P<0.05).The effects on 22RV1/DTX cells and pathways were reversed by ERK activator (P<0.05). Conclusions BBR may inhibit the proliferation, migration, and invasion of drug-resistant cells, promote cell apoptosis and thus enhance the chemotherapy sensitivity of prostate cancer cells to DTX with underlying mechanism of suppressing the ERK/ELK1 signaling pathway.

Key words: berberine, ERK/ELK1, prostate cancer cell, chemotherapy sensitivity

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