Ibrahim Abeer Y, Youness Eman R, Mahmoud Manal G, Asker Mohsen S, El-Newary Samah A
Department of Medicinal and Aromatic Plants Research, National Research Centre, Giza, Egypt.
Department of Medical Biochemistry, Medical Research Division, National Research Centre, Giza, Egypt.
Breast Cancer (Auckl). 2020 Jan 24;14:1178223420902075. doi: 10.1177/1178223420902075. eCollection 2020.
This study was planned to investigate the anti-breast-cancer property of acidic exopolysaccharide produced from marine 3MS 2017 (BAEPS) in an animal model, which previously showed in-vitro anti-breast-cancer activity, by studying its potential participation in various targeted mechanisms.
Mammary carcinoma in female Sprague-Dawley rats, both in prophylactic and in curative designs, was chemically induced using 7,12-dimethylebenz-(a)-anthracene (DMBA). 3MS 2017 anti-breast-cancer property was evaluated by studying its effects on cancer-growth-rate-limiting enzymes (aromatase and Na/K ATPase), sexual hormones (estrogen and progesterone), antioxidant and inflammatory biomarkers (cyclooxygenase-1; COX-1 and cyclooxygenase-2; COX-2). The incidence of breast cancer by DMBA was dependent on the level of carcinoembryonic antigen (CEA) and aromatase.
7,12-Dimethylebenz-(a)-anthracene female rats were characterized by a significant increase in cancer-related biomarkers with an increase of oxidative stress biomarkers, in comparison with the negative control. Potent BAEPS anticancer activity on DMBA rats was exhibited either as a prophylactic or as a curative agent, which appeared via restoring the aromatase and Na/K ATPase subunits levels and CEA close to the normal level. Besides, BAEPS modulated a sexual hormone, in comparison with the cancer control group ( ⩽ .05). 3MS 2017 selectively inhibited COX-2 in parallel with promising antioxidant properties. The curative characters of BAEPS were more promising than the prophylactic.
The anti-breast-cancer characters accompanied with a good safety margin may be attributed to its inhibitory effect on cancer-growth-rate-limiting enzymes, estrogen production, COX-2 level and lipid peroxidation, concurrent with enhancing COX-1 level, progesterone production, and antioxidant status.
本研究旨在通过研究其在各种靶向机制中的潜在作用,调查海洋来源的3MS 2017酸性胞外多糖(BAEPS)在动物模型中的抗乳腺癌特性,该多糖先前已显示出体外抗乳腺癌活性。
在雌性Sprague-Dawley大鼠中,采用7,12-二甲基苯并(a)蒽(DMBA)进行化学诱导,建立预防性和治疗性乳腺癌模型。通过研究BAEPS对癌症生长速率限制酶(芳香化酶和钠钾ATP酶)、性激素(雌激素和孕酮)、抗氧化和炎症生物标志物(环氧化酶-1;COX-1和环氧化酶-2;COX-2)的影响,评估其抗乳腺癌特性。DMBA诱导的乳腺癌发病率取决于癌胚抗原(CEA)和芳香化酶水平。
与阴性对照组相比,7,12-二甲基苯并(a)蒽雌性大鼠的癌症相关生物标志物显著增加,氧化应激生物标志物也增加。BAEPS作为预防性或治疗性药物,对DMBA大鼠均表现出强大的抗癌活性,其作用途径是使芳香化酶和钠钾ATP酶亚基水平以及CEA恢复至接近正常水平。此外,与癌症对照组相比,BAEPS调节了一种性激素(P≤0.05)。3MS 2017在具有良好抗氧化特性的同时,选择性抑制COX-2。BAEPS的治疗效果比预防效果更显著。
BAEPS的抗乳腺癌特性及其良好的安全性可能归因于其对癌症生长速率限制酶、雌激素生成、COX-2水平和脂质过氧化的抑制作用,同时增强了COX-1水平、孕酮生成和抗氧化状态。