首页> 美国卫生研究院文献>Experimental and Therapeutic Medicine >Ursolic acid inhibits breast cancer growth by inhibiting proliferation inducing autophagy and apoptosis and suppressing inflammatory responses via the PI3K/AKT and NF-κB signaling pathways in vitro
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Ursolic acid inhibits breast cancer growth by inhibiting proliferation inducing autophagy and apoptosis and suppressing inflammatory responses via the PI3K/AKT and NF-κB signaling pathways in vitro

机译:熊果酸通过在体外抑制增殖诱导自噬和凋亡并通过PI3K / AKT和NF-κB信号通路抑制炎症反应来抑制乳腺癌的生长

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摘要

Breast cancer, which is the second leading cause of cancer-associated mortality in women worldwide, develops from breast tissue. Chemotherapy is the most commonly used therapy to treat breast cancer. However, a number of natural plant-derived products have been suggested as alternative therapies to treat different types of cancer, such as breast cancer. The aim of the present study was to determine the anti-tumor effects of ursolic acid and its effect on apoptosis and inflammation in breast cancer cells. The anti-cancer effects of ursolic acid were evaluated in vitro using flow cytometry, western blotting and reverse transcription-quantitative polymerase chain reaction. The results suggest that ursolic acid inhibits the viability of breast cancer cells by inducing autophagy and apoptosis without inducing cell death. Cellular migration assays demonstrated that ursolic acid was able to suppress the invasive ability of breast cancer cells (P<0.05). In addition, the phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) pathway was downregulated following ursolic acid administration (P<0.05), leading to an upregulation of glycogen synthase kinase activity (P<0.05) and downregulation of B-cell lymphoma 2 (P<0.05), subsequently causing autophagy and apoptosis via cyclin-D1 inhibition and caspase-3 stimulation (P<0.05). Furthermore, the inflammatory response of breast cancer cells was assessed by measuring levels of nuclear factor (NF)-κB. Ursolic acid was found to downregulate NF-κB in breast cancer cells, thus inhibiting inflammation and preventing the progression of breast cancer (P<0.05). To the best of our knowledge, the present study is the first to assess the effect of ursolic acid on breast cancer cells through PI3K/AKT-regulated GSK and caspase-3 accompanied by NF-κB signaling pathways. The results of the present study regarding the potential underlying molecular mechanisms of ursolic acid may be used to develop novel therapeutic strategies for breast cancer treatment.
机译:乳腺癌是全世界女性与癌症相关的第二大死亡原因,其起源于乳房组织。化学疗法是治疗乳腺癌的最常用疗法。然而,已经提出了许多天然植物来源的产品作为治疗不同类型的癌症例如乳腺癌的替代疗法。本研究的目的是确定熊果酸的抗肿瘤作用及其对乳腺癌细胞凋亡和炎症的作用。使用流式细胞仪,蛋白质印迹和逆转录定量聚合酶链反应在体外评估了熊果酸的抗癌作用。结果表明,熊果酸通过诱导自噬和细胞凋亡而不诱导细胞死亡来抑制乳腺癌细胞的活力。细胞迁移试验表明熊果酸能够抑制乳腺癌细胞的侵袭能力(P <0.05)。此外,熊果酸给药后磷酸肌醇3-激酶(PI3K)/蛋白激酶B(AKT)通路被下调(P <0.05),导致糖原合酶激酶活性上调(P <0.05)和B-下调。细胞淋巴瘤2(P <0.05),随后通过细胞周期蛋白D1抑制和caspase-3刺激引起自噬和凋亡(P <0.05)。此外,通过测量核因子(NF)-κB的水平来评估乳腺癌细胞的炎症反应。发现熊果酸下调乳腺癌细胞中的NF-κB,从而抑制炎症并阻止乳腺癌的进展(P <0.05)。就我们所知,本研究是第一个通过PI3K / AKT调节的GSK和caspase-3以及NF-κB信号通路评估熊果酸对乳腺癌细胞的作用的研究。关于熊果酸的潜在潜在分子机制的本研究结果可用于开发乳腺癌治疗的新治疗策略。

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