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烷基溶血磷脂对人乳腺癌细胞系中表皮生长因子摄取的抑制作用与表皮生长因子内化的关系。

Inhibition by an alkyl-lysophospholipid of the uptake of epidermal growth factor in human breast cancer cell lines in relation to epidermal growth factor internalization.

作者信息

Kosano H, Takatani O

机构信息

Third Department of Internal Medicine, National Defense Medical College, Saitama, Japan.

出版信息

Cancer Res. 1989 Jun 1;49(11):2868-70.

PMID:2785846
Abstract

The effects of 1-O-octadecyl-2-O-methyl-sn-glycerol-3-phosphocholine (ET-18-OCH3), an alkyl-lysophospholipid derivative, on the binding and uptake of labeled epidermal growth factor (EGF) in hormone-dependent (MCF-7 and ZR-75-1) and hormone-independent (BT-20) breast cancer cell lines were investigated at 4 degrees C and 37 degrees C. The total (bound and intracellular) EGF associated with breast cancer cells tested were largely temperature dependent. By pretreatment of the cells with ET-18-OCH3 (10 micrograms/ml) for 12 h, the EGF uptake at 37 degrees C was greatly reduced in both MCF-7 and ZR-75-1 (ET-18-OCH3-susceptible) but not in BT-20 (ET-18-OCH3-resistant) cell lines. The ET-18-OCH3 pretreatment slightly decreased the EGF uptake at 4 degrees C in MCF-7 and ZR-75-1 and had little effect on that in BT-20. The EGF binding at 37 degrees C was unaffected by ET-18-OCH3 in MCF-7 and BT-20 and slightly decreased in ZR-75-1. The EGF binding at 4 degrees C was not changed by ET-18-OCH3 in all cell lines tested. These results suggest that labeled EGF is taken up by the cells in a temperature-dependent manner and ET-18-OCH3 may inhibit this internalization process only in ET-18-OCH3-sensitive human breast cancer cell lines. It is inferrable that the inhibition of the internalization process for EGF may be one of the modes of antitumoral action of ET-18-OCH3.

摘要

研究了烷基溶血磷脂衍生物1-O-十八烷基-2-O-甲基-sn-甘油-3-磷酸胆碱(ET-18-OCH3)在4℃和37℃下对激素依赖性(MCF-7和ZR-75-1)及激素非依赖性(BT-20)乳腺癌细胞系中标记表皮生长因子(EGF)结合和摄取的影响。与所测试的乳腺癌细胞相关的总(结合和细胞内)EGF在很大程度上取决于温度。用ET-18-OCH3(10微克/毫升)预处理细胞12小时后,37℃时MCF-7和ZR-75-1(对ET-18-OCH3敏感)细胞系中的EGF摄取量大幅降低,但BT-20(对ET-18-OCH3耐药)细胞系中则未降低。ET-18-OCH3预处理使MCF-7和ZR-75-1在4℃时的EGF摄取量略有下降,对BT-20的EGF摄取量影响不大。37℃时,ET-18-OCH3对MCF-7和BT-20中的EGF结合没有影响,而使ZR-75-1中的EGF结合略有下降。在所有测试细胞系中,4℃时ET-18-OCH3均未改变EGF结合。这些结果表明,标记的EGF以温度依赖性方式被细胞摄取,ET-18-OCH3可能仅在对ET-18-OCH3敏感的人乳腺癌细胞系中抑制这种内化过程。可以推断,抑制EGF的内化过程可能是ET-18-OCH3抗肿瘤作用的模式之一。

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