首页> 外文期刊>Journal of medicinal food >Bitter melon (Momordica charantia) extract suppresses adrenocortical cancer cell proliferation through modulation of the apoptotic pathway, steroidogenesis, and insulin-like growth factor type 1 receptor/RAC-α serine/threonine-protein kinase signaling
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Bitter melon (Momordica charantia) extract suppresses adrenocortical cancer cell proliferation through modulation of the apoptotic pathway, steroidogenesis, and insulin-like growth factor type 1 receptor/RAC-α serine/threonine-protein kinase signaling

机译:苦瓜提取物通过调节细胞凋亡途径,类固醇生成和胰岛素样生长因子1型受体/RAC-α丝氨酸/苏氨酸-蛋白激酶信号传导来抑制肾上腺癌细胞的增殖

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摘要

Adrenocortical carcinomas are rare but present with extremely poor prognosis. One of the approaches to control cancer progression and reduce cancer risk is prevention through diet. Bitter melon is widely consumed as a vegetable and especially as a traditional medicine in many countries. In this study, we have used human and mouse adrenocortical cancer cells as an in vitro model to assess the efficacy of bitter melon extract (BME) as an anticancer agent. The protein concentrations of BME and other extracts were measured before use. First, BME treatment of adrenocortical cancer cells resulted in a significantly dose-dependent decrease in cell proliferation. However, we did not observe an antiproliferative effect in adrenocortical cancer cells treated with extracts from blueberry, zucchini, and acorn squash. Second, apoptosis of adrenocortical cancer cells was accompanied by increased caspase-3 activation and poly(ADP-ribose) polymerase cleavage. BME treatment enhanced cellular tumor antigen p53, cyclin-dependent kinase inhibitor 1A (also called p21), and cyclic AMP-dependent transcription factor-3 levels and inhibited G1/S-specific cyclin D1, D2, and D3, and mitogen-activated protein kinase 8 (also called Janus kinase) expression, suggesting an additional mechanism involving cell cycle regulation and cell survival. Third, BME treatment decreased the key proteins involved in steroidogenesis in adrenocortical cancer cells. BME treatment decreased the level of phosphorylation of cyclin-dependent kinase 7, which is required, at least in part, for steroidogenic factor 1 activation. Finally, we observed that BME treatment significantly reduced the level of insulin-like growth factor 1 receptor and its downstream signaling pathway as evidenced by lower levels of phosphorylated RAC-α serine/threonine-protein kinase. Taken together, these data illustrate the inhibitory effect of bitter melon on cell proliferation of adrenocortical cancer through modulation of diverse mechanisms.
机译:肾上腺皮质癌很少见,但预后极差。控制饮食发展和降低癌症风险的方法之一是通过饮食预防。在许多国家,苦瓜被广泛用作蔬菜,特别是作为传统药物。在这项研究中,我们已经使用人类和小鼠的肾上腺皮质癌细胞作为体外模型来评估苦瓜提取物(BME)作为抗癌药的功效。使用前测量BME和其他提取物的蛋白质浓度。首先,肾上腺皮质癌细胞的BME治疗导致细胞增殖的明显剂量依赖性下降。但是,我们没有观察到蓝莓,西葫芦和橡子南瓜提取物对肾上腺皮质癌细胞的抗增殖作用。其次,肾上腺皮质癌细胞的凋亡伴随着caspase-3激活的增加和聚(ADP-核糖)聚合酶的裂解。 BME治疗可增强细胞肿瘤抗原p53,细胞周期蛋白依赖性激酶抑制剂1A(也称为p21)和环状AMP依赖性转录因子3水平,并抑制G1 / S特异性细胞周期蛋白D1,D2和D3以及促分裂原激活蛋白激酶8(也称为Janus激酶)表达,提示涉及细胞周期调控和细胞存活的其他机制。第三,BME治疗降低了肾上腺皮质癌细胞中参与类固醇生成的关键蛋白。 BME处理降低了细胞周期蛋白依赖性激酶7的磷酸化水平,这至少部分是类固醇生成因子1激活所必需的。最后,我们观察到BME治疗显着降低了胰岛素样生长因子1受体及其下游信号传导途径的水平,磷酸化的RAC-α丝氨酸/苏氨酸蛋白激酶的水平较低证明了这一点。综上所述,这些数据说明苦瓜通过调节多种机制对肾上腺皮质癌细胞增殖的抑制作用。

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