诺匹莱素与来曲唑对乳腺癌MCF-7细胞芳香化酶活性及表达影响的比较

S. T. Rahideh, M. Keramatipour, M. Nourbakhsh, F. Koohdani, M. Hoseini, S. Talebi, F. Shidfar
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引用次数: 9

摘要

Nobiletin (NOB)是主要存在于柑橘类水果中的一种多甲氧基黄酮。芳香化酶或细胞色素P450 (CYP19)酶催化雌激素生物合成的最后一步和限速步骤。本研究旨在探讨NOB对MCF-7乳腺癌细胞中芳香化酶活性和表达的影响,并将其与来曲唑(LET)作为芳香化酶抑制剂进行比较。用3-(4,5-二甲基噻唑-2-基)- 2,5 -二苯基溴化四唑(MTT)测定细胞活力。根据雄激素底物睾酮转化为17β-雌二醇来测定芳香酶活性。采用实时荧光定量PCR检测CYP19基因表达。MTT实验表明,100 μmol/L浓度的NOB对细胞活力有明显的降低作用(P < 0.05)。NOB浓度为0.1 μmol/L时对芳香化酶有显著抑制作用(P = 0.013),其他浓度对芳香化酶无显著抑制作用。10 μmol/L NOB和1 μmol/L NOB处理48 h,分别显著提高(P = 0.001)和降低(P = 0.02)相对芳香化酶表达。LET和NOB对芳香化酶无显著影响。本研究首次发现低浓度NOB可降低MCF-7乳腺癌细胞中芳香化酶的活性和表达。
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Comparison of the effects of nobiletin and letrozole on the activity and expression of aromatase in the MCF-7 breast cancer cell line.
Nobiletin (NOB) is one of the polymethoxyflavones mainly found in citrus fruits. Aromatase or cytochrome P450 (CYP19) enzyme catalyzes the last and rate-limiting step in estrogen biosynthesis. This study was carried out to investigate the effect of NOB on the activity and expression of aromatase, and to compare this property with letrozole (LET) as aromatase inhibitor in the MCF-7 breast cancer cell line. Cell viability was assessed with 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide (MTT) assays. Aromatase enzyme activity based on the conversion of androgenic substrate testosterone into 17β-estradiol was determined. CYP19 gene expression was measured by quantitative real-time PCR. MTT assays demonstrated that NOB at a concentration of 100 μmol/L decreased cell viability in a time-dependent manner (P < 0.05). NOB significantly inhibited aromatase at the concentration of 0.1 μmol/L (P = 0.013), whereas other concentrations had no effect. Treatment with 10 μmol/L and 1 μmol/L of NOB for 48 h significantly increased (P = 0.001) and decreased (P = 0.02) relative aromatase expression, respectively. The combination of LET and NOB had no effect on aromatase. This study showed for the first time that NOB decreases the activity and expression of aromatase at low concentrations in MCF-7 breast cancer cells.
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