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铁螯合作用:破解癌症治疗的新分子靶点。铁调节分子网络的冰山一角。

Iron chelation: deciphering novel molecular targets for cancer therapy. The tip of the iceberg of a web of iron-regulated molecules.

机构信息

Iron Metabolism & Chelation Program, Department of Pathology & Bosch Institute, BlackburnBuilding (D06), University of Sydney, Sydney, New South Wales, 2006 Australia.

出版信息

Future Med Chem. 2011 Dec;3(16):1983-6. doi: 10.4155/fmc.11.154.

Abstract

The response of cells to cellular iron depletion is complex with multiple molecules and signaling pathways being involved. Indeed, this is far broader than just the effect on the classical target, ribonucleotide reductase. It is likely that a network of interactions exists between the molecular players and that the relationships currently known only represent the ‘tip of an iceberg’ in terms of understanding the response of cells to iron deprivation. This article describes some of the research being undertaken in this area by the Richardson group at the University of Sydney, Australia [corrected].

摘要

细胞对细胞内铁耗竭的反应很复杂,涉及多种分子和信号通路。事实上,这远远超出了对经典靶标核糖核苷酸还原酶的影响。分子参与者之间可能存在着相互作用网络,而且目前已知的关系仅代表理解细胞对铁剥夺反应的“冰山一角”。本文描述了澳大利亚悉尼大学 Richardson 小组在这一领域所进行的部分研究[已更正]。

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