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Anti-Inflammatory Mechanism Involved in Pomegranate-Mediated Prevention of Breast Cancer: the Role of NF-κB and Nrf2 Signaling Pathways

机译:石榴介导的乳腺癌的抗炎机制:NF-κB和Nrf2信号通路的作用

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摘要

Pomegranate (Punica granatum L.), a nutrient-rich unique fruit, has been used for centuries for the prevention and treatment of various inflammation-driven diseases. Based on our previous study, a characterized pomegranate emulsion (PE) exhibited a striking inhibition of dimethylbenz(a)anthracene (DMBA)-initiated rat mammary tumorigenesis via antiproliferative and apoptosis-inducing mechanisms. The objective of the present work is to investigate the anti-inflammatory mechanism of action of PE during DMBA rat mammary carcinogenesis by evaluating the expression of cyclooxygenase-2 (COX-2), heat shock protein 90 (HSP90), nuclear factor-κB (NF-κB) and nuclear factor erythroid 2p45 (NF-E2)-related factor 2 (Nrf2). Mammary tumor samples were harvested from our previous chemopreventive study in which PE (0.2–5.0 g/kg) was found to reduce mammary tumorigenesis in a dose-dependent manner. The expressions of COX-2, HSP90, NF-κB, inhibitory κBα (IκBα) and Nrf2 were detected by immunohistochemical techniques. PE decreased the expression of COX-2 and HSP90, prevented the degradation of IκBα, hindered the translocation of NF-κB from cytosol to nucleus and increased the expression and nuclear translocation of Nrf2 during DMBA-induced mammary tumorigenesis. These findings, together with our previous results, indicate that PE-mediated prevention of DMBA-evoked mammary carcinogenesis may involve anti-inflammatory mechanisms through concurrent but differential regulation of two interrelated molecular pathways, namely NF-κB and Nrf2 signaling.
机译:石榴(Punica granatum L.)是一种营养丰富的独特水果,几个世纪以来一直用于预防和治疗各种炎症引起的疾病。根据我们先前的研究,特征性的石榴乳液(PE)通过抗增殖和凋亡诱导机制对二甲基苯并蒽(DMBA)引发的大鼠乳腺肿瘤发生具有显着抑制作用。本工作的目的是通过评估环氧合酶2(COX-2),热休克蛋白90(HSP90),核因子-κB(CX)的表达来研究PE在DMBA大鼠乳腺癌发生过程中的抗炎作用机制。 NF-κB)和核因子红系2p45(NF-E2)相关因子2(Nrf2)。乳腺肿瘤样品是从我们先前的化学预防研究中收集的,在该研究中,发现PE(0.2–5.0 g / kg)以剂量依赖性方式减少了乳腺肿瘤的发生。免疫组化技术检测COX-2,HSP90,NF-κB,抑制性κBα(IκBα)和Nrf2的表达。 PE降低了DMBA诱导的乳腺肿瘤发生过程中COX-2和HSP90的表达,阻止了IκBα的降解,阻碍了NF-κB从胞质向核的转运,并增加了Nrf2的表达和核转运。这些发现以及我们以前的研究结果表明,PE介导的DMBA诱发的乳癌发生的预防可能通过同时但不同的两个相互关联的分子途径(即NF-κB和Nrf2信号传导)的调控来涉及抗炎机制。

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