Suppr超能文献

类固醇和视黄酸对人乳腺癌细胞花生凝集素结合的影响。

Influence of steroids and retinoic acid on peanut-lectin binding of human breast cancer cells.

作者信息

Daxenbichler G, Dürken M, Marth C, Böck G, Dapunt O

出版信息

J Steroid Biochem. 1986 Jan;24(1):119-24. doi: 10.1016/0022-4731(86)90040-3.

Abstract

Membrane binding sites for peanut lectin or peanut agglutinin (PNA) were investigated in the established mammary carcinoma cell lines MCF-7, 734-B, ZR-75.1 and BT-20. The determination of PNA binding sites was performed in a flow cytometer after staining with fluorescein(FITC)-labeled PNA. It appeared that only the estrogen-sensitive cell lines exhibited PNA binding sites, whereas the hormone-insensitive cell line BT-20 was clearly negative. Steroid hormones, when administered singly to the cells in physiological concentrations (10(-9)-10(-8) M) had no effect on PNA binding expression. Only the combination of estradiol and progesterone together increased PNA binding sites. Pharmacological doses (10(-6) M) of medroxyprogesteroneacetate (MPA) and dexamethasone increased the number of binding sites, whereas retinoic acid decreased them. A preliminary characterization of the binding sites revealed that they have high capacity and moderate affinity for PNA (KD greater than 10(-7) M). FITC-PNA binding could be inhibited selectively by fetuin (greater than 10(-5) M) and by galactose (greater than 10(-2) M). Cytosol from MCF-7 cells and from some primary breast cancer specimens were able to decrease PNA binding to the surface of 734-B cells.

摘要

在已建立的乳腺癌细胞系MCF-7、734-B、ZR-75.1和BT-20中研究了花生凝集素或花生凝集素(PNA)的膜结合位点。在用异硫氰酸荧光素(FITC)标记的PNA染色后,在流式细胞仪中进行PNA结合位点的测定。结果显示,只有雌激素敏感的细胞系表现出PNA结合位点,而激素不敏感的细胞系BT-20明显为阴性。当以生理浓度(10(-9)-10(-8)M)单独给予细胞时,类固醇激素对PNA结合表达没有影响。只有雌二醇和孕酮联合使用才会增加PNA结合位点。醋酸甲羟孕酮(MPA)和地塞米松的药理剂量(10(-6)M)增加了结合位点的数量,而视黄酸则使其减少。结合位点的初步特征表明,它们对PNA具有高容量和中等亲和力(KD大于10(-7)M)。FITC-PNA结合可被胎球蛋白(大于10(-5)M)和半乳糖(大于10(-2)M)选择性抑制。MCF-7细胞和一些原发性乳腺癌标本的胞质溶胶能够减少PNA与734-B细胞表面的结合。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验