Molecular markers for prediction of risk of radiation-related injury to normal tissue

M. Ghilotti, M. Pierotti, M. Gariboldi
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引用次数: 7

Abstract

Radiotherapy is one of the most effective methods for the treatment of cancer, but occurrence of adverse reactions developing in the co-irradiated normal tissue can be a threat for patients. Identification of individuals at risk of severe reaction is very difficult and considerable efforts have been made to correlate normal tissue toxicity with cellular responses to ionizing radiation. Genetic markers enabling to identify hyper-sensitive patients prior to treatment would considerably improve its outcome. Gene association studies should help to identify such markers. Expression levels of specific transcripts could be putative markers; in fact different studies found associations between gene expression profiles in normal cells and the reaction of normal tissues to radiation therapy. The finding that ionizing radiation induces the deregulation of a high number of genes suggests that also microRNAs that affect the expression of a large number of target genes may be involved. This review briefly introduces the mechanisms of radiation-induced normal tissue toxicity and summarizes clinical research focused on the evaluation of molecular biomarkers for predicting risk of injury to normal tissue, mainly describing gene transcripts alterations.
用于预测正常组织辐射相关损伤风险的分子标记
放射治疗是治疗癌症最有效的方法之一,但在共照射的正常组织中发生的不良反应可能对患者构成威胁。识别有严重反应风险的个体是非常困难的,人们已经做出了相当大的努力,将正常组织毒性与细胞对电离辐射的反应联系起来。能够在治疗前识别超敏感患者的遗传标记将大大改善其结果。基因关联研究应该有助于识别这些标记。特异转录物的表达水平可以作为推测的标记物;事实上,不同的研究发现了正常细胞的基因表达谱与正常组织对放射治疗的反应之间的联系。电离辐射诱导大量基因解除调控的发现表明,影响大量靶基因表达的microrna也可能参与其中。本文简要介绍了辐射诱导正常组织毒性的机制,并总结了用于预测正常组织损伤风险的分子生物标志物的临床研究,主要描述了基因转录物的改变。
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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