在实验模型和临床人群中,铁调节 MHC I 类分子 HFE 对肿瘤进展的影响证据。

Translational oncogenomics Pub Date : 2014-12-04 eCollection Date: 2014-01-01 DOI:10.4137/TOG.S19064
Cody Weston, James Connor
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引用次数: 0

摘要

参与铁调节的蛋白质是癌症风险和进展的调节因子。其中,HFE 蛋白(高铁基因及其蛋白产物)尤其引人关注,因为它与铁处理和免疫功能都有相互作用,而且基因多态性导致突变蛋白的发生率很高。临床研究表明,HFE 多态性会增加罹患某些癌症的风险,但不一致的结果表明其影响更为微妙,可能与其他遗传或环境因素相互作用。目前已经开展了一些基础科学研究,开始了解变异 HFE 基因型对癌症的影响,但研究还远远没有完成。特别是,HFE 通过其在铁处理中的作用及其主要组织相容性复合体 I 类结构特征影响肿瘤进展的推测机制是存在的。本综述介绍了目前对 HFE 在癌症中作用的理解,并确定了未来研究方向的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Evidence for the Influence of the Iron Regulatory MHC Class I Molecule HFE on Tumor Progression in Experimental Models and Clinical Populations.

Proteins involved in iron regulation are modifiers of cancer risk and progression. Of these, the HFE protein (high iron gene and its protein product) is of particular interest because of its interaction with both iron handling and immune function and the high rate of genetic polymorphisms resulting in a mutant protein. Clinical studies suggest that HFE polymorphisms increase the risk of certain cancers, but the inconsistent outcomes suggest a more nuanced effect, possibly interacting with other genetic or environmental factors. Some basic science research has been conducted to begin to understand the implications of variant HFE genotype on cancer, but the story is far from complete. In particular, putative mechanisms exist for HFE to affect tumor progression through its role in iron handling and its major histocompatibility complex class I structural features. In this review, the current understanding of the role of HFE in cancer is described and models for future directions are identified.

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