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纳维托昔单抗(Bcl-2 和 Bcl-xL 抑制剂)与 Debio-0932(热休克蛋白 90 抑制剂)联合应用通过诱导凋亡信号通路抑制前列腺癌细胞的活力。

Combination of navitoclax (Bcl-2 and Bcl-xL inhibitor) and Debio-0932 (Hsp90 inhibitor) suppresses the viability of prostate cancer cells via induction of apoptotic signaling pathway.

机构信息

Faculty of Medicine, Department of Urology, Sivas Cumhuriyet University, Sivas, Turkey.

Artova Vocational School, Department of Veterinary Medicine, Laboratory and Veterinary Health Program, Tokat Gaziosmanpasa University, Tokat, Turkey.

出版信息

Med Oncol. 2024 Mar 4;41(4):83. doi: 10.1007/s12032-024-02335-3.

DOI:10.1007/s12032-024-02335-3
PMID:38436810
Abstract

Prostate cancer is one of the most common cancers in men. Given the diverse nature of prostate cancer and its tendency to respond differently to various treatments, combination therapies are often employed to enhance outcomes. In this study, the synergetic efficiency of chemotherapeutic drug Navitoclax and heat shock protein 90 (Hsp90) inhibitor Debio-0932 was evaluated in human prostate cancer cell line (PC3). Our results indicated that Navitoclax-Debio-0932 combination exhibited synergistic activity in PC3 cells at concentrations lower than IC values. The combination of Navitoclax and Debio-0932 decreased PC3 cell viability in a dose dependent manner at 48 h. To investigate the apoptotic potential of the Navitoclax-Debio-0932 combination against prostate cancer cells, the mRNA and protein expression levels of apoptotic and antiapoptotic markers (Bax, Bcl-2, Bcl-xL, Cyt-c, Apaf-1, Casp-3, Casp-7, and Casp-9) were measured using RT-PCR and ELISA assay. Furthermore, the cleavage activity of Casp-3 was determined by colorimetric assay. The results revealed that Navitoclax-Debio-0932 combination potently induced intrinsic apoptotic pathway in PC3 cells rather than using drugs alone. The combined treatment of Navitoclax and Debio-0932 displayed synergistic cytotoxic and apoptotic effects on prostate cancer cells, presenting a promising approach for combination therapy in prostate cancer.

摘要

前列腺癌是男性最常见的癌症之一。鉴于前列腺癌的多样性及其对各种治疗方法的反应不同,通常采用联合治疗来提高疗效。在这项研究中,评估了化疗药物 Navitoclax 和热休克蛋白 90(Hsp90)抑制剂 Debio-0932 对人前列腺癌细胞系(PC3)的协同效率。我们的结果表明,Navitoclax-Debio-0932 联合在低于 IC 值的浓度下在 PC3 细胞中表现出协同活性。Navitoclax 和 Debio-0932 的组合以剂量依赖的方式在 48 小时内降低了 PC3 细胞活力。为了研究 Navitoclax-Debio-0932 联合对前列腺癌细胞的凋亡潜力,使用 RT-PCR 和 ELISA 测定法测量了凋亡和抗凋亡标志物(Bax、Bcl-2、Bcl-xL、Cyt-c、Apaf-1、Casp-3、Casp-7 和 Casp-9)的 mRNA 和蛋白表达水平。此外,通过比色法测定 Casp-3 的裂解活性。结果表明,Navitoclax-Debio-0932 联合强烈诱导了 PC3 细胞中的内在凋亡途径,而不是单独使用药物。Navitoclax 和 Debio-0932 的联合治疗对前列腺癌细胞表现出协同的细胞毒性和凋亡作用,为前列腺癌的联合治疗提供了一种有前途的方法。

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本文引用的文献

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The effects of STA-9090 (Ganetespib) and venetoclax (ABT-199) combination on apoptotic pathways in human cervical cancer cells.STA-9090(Ganetespib)和 Venetoclax(ABT-199)联合对人宫颈癌细胞凋亡途径的影响。
Med Oncol. 2023 Jul 11;40(8):234. doi: 10.1007/s12032-023-02107-5.
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Characterisation of cell lines derived from prostate cancer patients with localised disease.源自局限性前列腺癌患者的细胞系的特征。
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A Phase I Study of Capivasertib in Combination With Abiraterone Acetate in Patients With Metastatic Castration-Resistant Prostate Cancer.卡匹西利联合醋酸阿比特龙治疗转移性去势抵抗性前列腺癌的I期研究
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Navitoclax Most Promising BH3 Mimetic for Combination Therapy in Hodgkin Lymphoma.纳维托昔单抗:最有前途的 Hodgkin 淋巴瘤联合治疗中的 BH3 模拟物。
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Drug Combination Modeling: Methods and Applications in Drug Development.药物组合建模:药物研发中的方法与应用
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Prostate Cancer Review: Genetics, Diagnosis, Treatment Options, and Alternative Approaches.前列腺癌综述:遗传学、诊断、治疗选择和替代方法。
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