巴西莓提取物在雄激素依赖性和非依赖性前列腺癌细胞中诱导炎症和免疫反应的差异

IF 2.5 Q3 ONCOLOGY Journal of Cancer Prevention Pub Date : 2022-09-30 DOI:10.15430/JCP.2022.27.3.182
Larissa Akemi Kido, Isabela Maria Urra Rossetto, Andressa Mara Baseggio, Gabriela Bortolanza Chiarotto, Letícia Ferreira Alves, Felipe Rabelo Santos, Celina de Almeida Lamas, Mário Roberto Maróstica Jr, Valéria Helena Alves Cagnon
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摘要

Jaboticaba是一种巴西浆果,富含纤维和生物活性化合物,具有较高的抗氧化和抗增殖活性。前列腺癌(PCa)是男性中第二常见的癌症类型,其进展受雄激素和炎症的影响。先前的研究报道了jaboticaba调节前列腺疾病相关通路的能力。本研究的主要目的是提供JPE在不同雄激素状态PCa细胞系(LNCaP和PC-3)中的分子靶点及其作用机制的重要数据。结果表明,JPE能降低两种细胞系的细胞活力。LNCaP对JPE暴露更敏感,表明JPE治疗在雄激素反应方面的有效性。JPE对NF-κB信号通路表现出明显的激素依赖作用,LNCaP中NF-κB水平降低,PC-3细胞中NF-κB水平升高。JPE治疗后刺激细胞凋亡相关机制,调节LNCaP和PC-3的b细胞淋巴瘤2和BAX。特别是对于PC-3, JPE治疗主要通过上调促炎、促血管生成、免疫刺激和免疫抑制基因激活细胞因子-细胞因子受体相互作用。此外,JPE还下调了一系列与血管生成和转移相关的基因。综上所述,JPE对两种细胞系都有抗肿瘤作用,如果考虑雄激素依赖性,这种作用可以增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Brazilian Berry Extract Differentially Induces Inflammatory and Immune Responses in Androgen Dependent and Independent Prostate Cancer Cells.

Jaboticaba is a Brazilian berry, which is rich in fibers and bioactive compounds and shows high antioxidant and antiproliferative activities. Prostate cancer (PCa) is the second most common type of cancer among men and its progression is influenced by androgens and inflammation. Previous studies reported the ability of the jaboticaba to modulate pathways involved in prostate diseases. The main objective of this study was to provide significant data about molecular targets of the jaboticaba peel extract (JPE) and its mechanisms of action in PCa cell lines with different androgenic status (LNCaP and PC-3). The results showed that JPE was able to decrease cell viability in both cell lines. LNCaP showed more sensitivity to JPE exposure, indicating the efficacy of the JPE treatment in terms of androgen responsiveness. JPE showed a distinct hormone dependent effect on the NF-κB signaling, with reduced NF-κB levels for LNCaP and increased NF-κB levels in PC-3 cells. Mechanisms related to cell death by apoptosis were stimulated after the JPE treatment, modulating B-cell lymphoma 2 and BAX for LNCaP and PC-3. Particularly for PC-3, the JPE treatment resulted in cytokine-cytokine receptor interaction activation mostly by up regulating pro-inflammatory, pro-angiogenic, immunostimulatory and immunosuppressive genes. Also, a set of genes related to angiogenesis and metastasis were down-regulated by JPE. In conclusion, JPE exerted an antitumor effect on PCa for both cell lines which can be enhanced if androgenic reliance is considered.

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