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神经母细胞瘤细胞对间碘苄胍的摄取是由独立的摄取和储存机制导致的。

Accumulation of m-iodobenzylguanidine by neuroblastoma cells results from independent uptake and storage mechanisms.

作者信息

Montaldo P G, Lanciotti M, Casalaro A, Cornaglia-Ferraris P, Ponzoni M

机构信息

Pediatric Oncology Research Laboratory, G. Gaslini Children's Hospital, Genoa, Italy.

出版信息

Cancer Res. 1991 Aug 15;51(16):4342-6.

PMID:1868458
Abstract

The modalities of uptake and storage of iodine-labeled m-iodobenzylguanidine (MIBG) by four human neuroblastoma cell lines have been studied. SK-N-BE(2)C cell line has been shown to possess the specific (type 1) MIBG uptake, as well as an efficient extravesicular storage mechanism. Conversely, LAN-5 cells, which show a nonsaturation kinetic of MIBG incorporation, lack only the ability to efficiently store the MIBG taken up by a mechanism that can be pharmacologically defined as uptake 1. The two other neuroblastoma cell lines tested, GI-LI-N and GI-CA-N, lack both uptake and storage capacity. In view of the fact that the only detailed study on specific MIBG uptake by a human neuroblastoma cell line has been carried out on SK-N-SH, a highly heterogeneous cell line, our report provides new insights on the molecular and cellular pharmacology of radiolabeled MIBG.

摘要

对四种人神经母细胞瘤细胞系摄取和储存碘标记的间碘苄胍(MIBG)的方式进行了研究。已证明SK-N-BE(2)C细胞系具有特异性(1型)MIBG摄取以及高效的囊泡外储存机制。相反,表现出MIBG掺入非饱和动力学的LAN-5细胞仅缺乏通过一种可在药理学上定义为摄取1的机制有效储存所摄取MIBG的能力。测试的另外两种神经母细胞瘤细胞系GI-LI-N和GI-CA-N既缺乏摄取能力也缺乏储存能力。鉴于对人神经母细胞瘤细胞系特异性MIBG摄取的唯一详细研究是在高度异质性的SK-N-SH细胞系上进行的,我们的报告为放射性标记MIBG的分子和细胞药理学提供了新的见解。

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