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Polygodial analog induces apoptosis in LNCaP prostate cancer cells

机译:Polygodial类似物诱导LNCaP前列腺癌细胞凋亡

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摘要

Prostate cancer (PCa) is the second leading cause of death in American men. The chemotherapeutic treatment strategies are generally not effective and can lead to side effects. Hence, there is an urgent need to identify novel chemotherapeutic agents. The aim of this study was to synthesize and evaluate the therapeutic effects of a synthetic analog of polygodial (PG), a pungent constituent abundantly present in mountain pepper, water pepper and dorrigo pepper, on LNCaP PCa cell line and its anti-cancer mechanisms in a preclinical study. We evaluated the anti-cancer potential of the PG analog namely DRP-27 using various assays such as cell viability by MTT assay, anchorage independent growth by soft agar assay, reactive oxygen species generation by 2′,7′-dichlorofluorescein probe-based fluorescence assay, and apoptosis by Annexin-V and TUNEL assays respectively. Western blot analysis was performed to identify the molecular mechanism of DRP-27-induced cell death. Our results showed that DRP-27 significantly inhibited LNCaP cell proliferation in a dose-dependent manner at 48 h treatment in vitro. In addition, DRP-27 potently inhibited anchorage-independent growth of these cells. Flow cytometry, Annexin-V and TUNEL assays confirmed that DRP-27 induces apoptosis in LNCaP cells. DRP-27 also induced the activation of intracellular reactive oxygen species. Western blot analysis revealed that DRP-27 downregulated the expression of survivin, while activating Bax and DNA damage marker pH2AX in LNCaP cells. In conclusion, our study suggests that DRP-27 might be an effective anti-cancer agent for PCa.
机译:前列腺癌(PCa)是美国男性的第二大死亡原因。化疗治疗策略通常无效,并且可能导致副作用。因此,迫切需要鉴定新的化学治疗剂。这项研究的目的是合成和评估合成的多果体(PG)类似物对LNCaP PCa细胞系的治疗作用及其抗癌机制,该合成物在山胡椒,水胡椒和多雷哥胡椒中大量存在。临床前研究。我们使用各种测定法评估了PG类似物即DRP-27的抗癌潜力,例如通过MTT测定法测定细胞活力,通过软琼脂测定法测定锚定非依赖性生长,通过基于2',7'-dichlorofluorescein探针的荧光产生活性氧膜联蛋白-V和TUNEL分析分别检测细胞凋亡和凋亡。进行蛋白质印迹分析以鉴定DRP-27诱导的细胞死亡的分子机制。我们的结果表明,DRP-27在体外治疗48 h时以剂量依赖性方式显着抑制LNCaP细胞增殖。此外,DRP-27有效抑制了这些细胞的锚定非依赖性生长。流式细胞仪,Annexin-V和TUNEL分析证实DRP-27诱导LNCaP细胞凋亡。 DRP-27还诱导了细胞内活性氧的活化。蛋白质印迹分析表明,DRP-27在激活LNCaP细胞中的Bax和DNA损伤标记pH2AX的同时下调了survivin的表达。总之,我们的研究表明DRP-27可能是PCa的有效抗癌药。

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