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葡萄籽原花青素对联合暴露于 4-(甲基亚硝氨基)-1-(3-吡啶基)-1-丁酮和苯并[a]芘引起的乳腺细胞癌变的抑制作用。

Grape seed proanthocyanidin suppression of breast cell carcinogenesis induced by chronic exposure to combined 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone and benzo[a]pyrene.

机构信息

Department of Comparative Medicine, College of Veterinary Medicine, University of Tennessee, Knoxville, Tennessee 37996, USA.

出版信息

Mol Carcinog. 2010 May;49(5):450-63. doi: 10.1002/mc.20616.

Abstract

Breast cancer is the most common type of cancer among women in northern America and northern Europe; dietary prevention is a cost-efficient strategy to reduce the risk of this disease. To identify dietary components for the prevention of human breast cancer associated with long-term exposure to environmental carcinogens, we studied the activity of grape seed proanthocyanidin extract (GSPE) in suppression of cellular carcinogenesis induced by repeated exposures to low doses of environmental carcinogens. We used combined carcinogens 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and benzo[a]pyrene (B[a]P), at picomolar concentrations, to repeatedly treat noncancerous, human breast epithelial MCF10A cells to induce cellular acquisition of cancer-related properties of reduced dependence on growth factors, anchorage-independent growth, and acinar-conformational disruption. Using these properties as biological target endpoints, we verified the ability of GSPE to suppress combined NNK- and B[a]P-induced precancerous cellular carcinogenesis and identified the minimal, noncytotoxic concentration of GSPE required for suppressing precancerous cellular carcinogenesis. We also identified that hydroxysteroid-11-beta-dehydrogenase 2 (HSD11B2) may play a role in NNK- and B[a]P-induced precancerous cellular carcinogenesis, and its expression may act as a molecular target endpoint in GSPE's suppression of precancerous cellular carcinogenesis. And, the ability of GSPE to reduce gene expression of cytochrome-P450 enzymes CYP1A1 and CYP1B1, which can bioactivate NNK and B[a]P, possibly contributes to the preventive mechanism for GSPE in suppression of precancerous cellular carcinogenesis. Our model system with biological and molecular target endpoints verified the value of GSPE for the prevention of human breast cell carcinogenesis induced by repeated exposures to low doses of multiple environmental carcinogens.

摘要

乳腺癌是北美和北欧地区女性最常见的癌症类型;饮食预防是降低这种疾病风险的一种具有成本效益的策略。为了确定预防与长期暴露于环境致癌物相关的人类乳腺癌的饮食成分,我们研究了葡萄籽原花青素提取物 (GSPE) 在抑制低剂量环境致癌物反复暴露诱导的细胞癌变中的活性。我们使用组合致癌物 4-(甲基亚硝氨基)-1-(3-吡啶基)-1-丁酮 (NNK) 和苯并[a]芘 (B[a]P),以皮摩尔浓度,反复处理非癌性、人乳腺上皮 MCF10A 细胞,以诱导细胞获得与癌症相关的特性,包括对生长因子的依赖性降低、非锚定依赖性生长和腺泡构象破坏。使用这些特性作为生物靶终点,我们验证了 GSPE 抑制 NNK 和 B[a]P 联合诱导的癌前细胞癌变的能力,并确定了抑制癌前细胞癌变所需的最小非细胞毒性 GSPE 浓度。我们还发现羟甾类 11-β-脱氢酶 2 (HSD11B2) 可能在 NNK 和 B[a]P 诱导的癌前细胞癌变中发挥作用,其表达可能作为 GSPE 抑制癌前细胞癌变的分子靶终点。而且,GSPE 降低细胞色素 P450 酶 CYP1A1 和 CYP1B1 的基因表达的能力,这些酶可以使 NNK 和 B[a]P 生物活化,可能有助于 GSPE 在抑制癌前细胞癌变中的预防机制。我们的具有生物学和分子靶终点的模型系统验证了 GSPE 用于预防反复低剂量暴露于多种环境致癌物诱导的人类乳腺细胞癌变的价值。

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