胶质母细胞瘤的风险因素与其他脑肿瘤类型相同。

Carr J Smith, Thomas A Perfetti, Chirayu Chokshi, Chitra Venugopal, J Wesson Ashford, Sheila K Singh
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引用次数: 0

摘要

已报道的胶质母细胞瘤(GBM)风险因素,即电离辐射、Li-Fraumeni 综合征、神经纤维瘤病 I 和 Turcot 综合征,也会增加其他类型脑肿瘤的风险。人类 GBM 的风险因素与不同的致癌突变特征有关。鼻子较短、面部较平的纯种家犬(肱骨犬)的胶质瘤形成率相对较高。犬类胶质瘤的遗传特征也具有特异性。人类和犬类胶质瘤的基因突变模式可能不同,这表明不同的致癌途径可能导致胶质瘤的形成。目前尚缺乏流行病学证据证明接触化学致癌物质与 GBM 发病风险增加之间存在关联。电离辐射会诱发点突变、框架转换突变、双链断裂以及染色体插入或缺失。与化学物质暴露相关的突变特征与电离辐射的广泛突变模式重叠。流行病学研究中报告的化学物质暴露与 GBM 之间的微弱统计学关联在生物学上是可信的。将自发性 GBM 的可重现模式与从已知大量接触潜在致癌化学品的患者身上切除的 GBM 中发现的类似模式进行比较的分子方法,可以解决传统接触评估所带来的困难。
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Risk factors for glioblastoma are shared by other brain tumor types.

The reported risk factors for glioblastoma (GBM), i.e., ionizing radiation, Li-Fraumeni syndrome, Neurofibromatosis I, and Turcot syndrome, also increase the risk of other brain tumor types. Risk factors for human GBM are associated with different oncogenic mutation profiles. Pedigreed domestic dogs with a shorter nose and flatter face (brachycephalic dogs) display relatively high rates of glioma formation. The genetic profiles of canine gliomas are also idiosyncratic. The association of putatively different mutational patterns in humans and canines with GBM suggests that different oncogenic pathways can result in GBM formation. Strong epidemiological evidence for an association between exposure to chemical carcinogens and an increased risk for development of GBM is currently lacking. Ionizing radiation induces point mutations, frameshift mutations, double-strand breaks, and chromosomal insertions or deletions. Mutational profiles associated with chemical exposures overlap with the broad mutational patterns seen with ionizing radiation. Weak statistical associations between chemical exposures and GBM reported in epidemiology studies are biologically plausible. Molecular approaches comparing reproducible patterns seen in spontaneous GBM with analogous patterns found in GBMs resected from patients with known significant exposures to potentially carcinogenic chemicals can address difficulties presented by traditional exposure assessment.

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