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Discriminating Gene Expression Signature of Radiation-Induced Thyroid Tumors after Either External Exposure or Internal Contamination

机译:区分辐射暴露或内部污染后辐射诱发的甲状腺肿瘤的基因表达特征。

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Both external radiation exposure and internal radionuclide contamination are well known risk factors in the development of thyroid epithelial tumors. The identification of specific molecular markers deregulated in radiation-induced thyroid tumors is important for the etiological diagnosis since neither histological features nor genetic alterations can discriminate between sporadic and radiation-induced tumors. Identification of highly discriminating markers in radiation-induced tumors is challenging as it relies on the ability to identify marker deregulation which is associated with a cellular stress that occurred many years before in the thyroid cells. The existence of such a signature is still controversial, as it was not found in several studies while a highly discriminating signature was found in both post-radiotherapy and post-Chernobyl series in other studies. Overall, published studies searching for radiation-induced thyroid tumor specificities, using transcriptomic, proteomic and comparative genomic hybridization approaches, and bearing in mind the analytical constraints required to analyze such small series of tumors, suggest that such a molecular signature could be found. In comparison with sporadic tumors, we highlight molecular similarities and specificities in tumors occurring after high-dose external radiation exposure, such as radiotherapy, and in post-Chernobyl tumors that occurred after internal 131I contamination. We discuss the relevance of signature extrapolation from series of tumors developing after high and low doses in the identification of tumors induced at very low doses of radiation.
机译:外部辐射暴露和内部放射性核素污染都是甲状腺上皮肿瘤发展的众所周知的危险因素。放射诱发的甲状腺肿瘤中失控的特定分子标记的鉴定对于病因学诊断很重要,因为组织学特征和遗传改变均不能区分散发性和放射诱发的肿瘤。在放射线诱发的肿瘤中鉴定高度区分的标记物具有挑战性,因为它依赖于鉴定标记物失调的能力,该失调与甲状腺细胞中多年以前发生的细胞应激有关。这种签名的存在仍存在争议,因为在几项研究中并未发现,而在其他放射治疗后和切尔诺贝利系列后两者中都发现了高度区分的签名。总体而言,已发表的研究使用转录组学,蛋白质组学和比较基因组杂交方法,寻找辐射诱发的甲状腺肿瘤特异性,并牢记分析此类小系列肿瘤所需的分析限制,表明可以找到这种分子标记。与散发性肿瘤相比,我们强调了在高剂量外部放射线照射(例如放疗)后发生的肿瘤以及内部 131 I污染后发生的切尔诺贝利后肿瘤中的分子相似性和特异性。我们讨论了从高剂量和低剂量后发展而来的一系列肿瘤的特征外推法在鉴定以极低剂量的辐射诱发的肿瘤中的相关性。

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