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γ-生育三烯酚与他汀类药物联合治疗可诱导乳腺肿瘤细胞周期在G1期停滞。

Combined treatment of gamma-tocotrienol with statins induce mammary tumor cell cycle arrest in G1.

作者信息

Wali Vikram B, Bachawal Sunitha V, Sylvester Paul W

机构信息

College of Pharmacy, University of Louisiana at Monroe, 700 University Avenue, Monroe, LA 71209-0470, USA.

出版信息

Exp Biol Med (Maywood). 2009 Jun;234(6):639-50. doi: 10.3181/0810-RM-300. Epub 2009 Apr 9.

Abstract

Statins and gamma-tocotrienol (a rare isoform of vitamin E) both inhibit 3-hydroxy-3-methylglutaryl-coenzyme A (HMGCoA) reductase activity and display anticancer activity. However, clinical application of statins has been limited by high dose toxicity. Previous studies showed that combined statin and gamma-tocotrienol treatment synergistically inhibits growth of highly malignant +SA mammary epithelial cells in culture. To investigate the mechanism mediating this growth inhibition, studies were conducted to determine the effect of combination low dose gamma-tocotrienol and statin treatment on +SA mammary tumor cell cycle progression. Treatment with 0.25 microM simvastatin, lovastatin, mevastatin, 10 microM pravastatin or 2.0 microM gamma-tocotrienol alone had no effect, while combined treatment of individual statins with gamma-tocotrienol significantly inhibited +SA cell proliferation during the 4-day culture period. Flow cytometric analysis demonstrated that combined treatment induced cell cycle arrest in G1. Additional studies showed that treatment with 0.25 microM simvastatin or 2 microM gamma-tocotrienol alone had no effect on the relative intracellular levels of cyclin D1, CDK2, CDK4 and CDK6, but combined treatment caused a large reduction in cyclin D1 and CDK2 levels. Combined treatments also caused a relatively large increase in p27, but had no effect on p21 and p15 levels, and resulted in a large reduction in retinoblastoma (Rb) protein phosphorylation at ser780 and ser807/811. Similar effects were observed following combined treatment of gamma-tocotrienol with low doses of lovastatin, mevastatin and pravastatin. These findings demonstrate that combination low dose statin and gamma-tocotrienol treatment induced mammary tumor cell cycle arrest at G1, resulting from an increase in p27 expression, and a corresponding decrease in cyclin D1, CDK2, and hypophosphorylation of Rb protein. These findings suggest that combined treatment of statins with gamma-tocotrienol may provide significant health benefits in the treatment of breast cancer in women, while avoiding myotoxicity associated with high dose statin monotherapy.

摘要

他汀类药物和γ-生育三烯酚(维生素E的一种罕见异构体)均能抑制3-羟基-3-甲基戊二酰辅酶A(HMGCoA)还原酶活性,并具有抗癌活性。然而,他汀类药物的临床应用受到高剂量毒性的限制。先前的研究表明,他汀类药物与γ-生育三烯酚联合治疗可协同抑制培养中的高恶性+SA乳腺上皮细胞的生长。为了研究介导这种生长抑制的机制,进行了多项研究以确定低剂量γ-生育三烯酚与他汀类药物联合治疗对+SA乳腺肿瘤细胞周期进程的影响。单独使用0.25微摩尔辛伐他汀、洛伐他汀、美伐他汀、10微摩尔普伐他汀或2.0微摩尔γ-生育三烯酚进行治疗均无效果,而将各他汀类药物与γ-生育三烯酚联合治疗在4天的培养期内显著抑制了+SA细胞增殖。流式细胞术分析表明,联合治疗诱导细胞周期停滞在G1期。进一步的研究表明,单独使用0.25微摩尔辛伐他汀或2微摩尔γ-生育三烯酚对细胞周期蛋白D1、细胞周期蛋白依赖性激酶2(CDK2)、细胞周期蛋白依赖性激酶4(CDK4)和细胞周期蛋白依赖性激酶6(CDK6)的相对细胞内水平没有影响,但联合治疗导致细胞周期蛋白D1和CDK2水平大幅降低。联合治疗还导致p27相对大幅增加,但对p21和p15水平没有影响,并导致视网膜母细胞瘤(Rb)蛋白在ser780和ser807/811处的磷酸化大幅降低。γ-生育三烯酚与低剂量洛伐他汀、美伐他汀和普伐他汀联合治疗后也观察到类似效果。这些发现表明,低剂量他汀类药物与γ-生育三烯酚联合治疗诱导乳腺肿瘤细胞周期停滞在G1期,这是由于p27表达增加,以及细胞周期蛋白D1、CDK2相应减少,以及Rb蛋白的低磷酸化所致。这些发现表明,他汀类药物与γ-生育三烯酚联合治疗可能在治疗女性乳腺癌方面带来显著的健康益处,同时避免与高剂量他汀类药物单一疗法相关的肌毒性。

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