融合基因作为肿瘤诊断和预测的生物标志物

Z. Bao, Ruichao Chai, Xing Liu, Jiayi Wang
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引用次数: 0

摘要

结构变异,包括染色体重排和易位,可能导致融合基因的形成。神经胶质瘤是成人中最常见的脑肿瘤。由于肿瘤分类复杂、复发特征、样本量不足以及肿瘤恶性机制存在争议,近30年来一直没有制定出临床策略。融合基因是胶质瘤发生的重要驱动因素之一,为胶质瘤的发病机制提供了基础性的认识。本文综述了融合基因的发现、检测技术的发展及其临床应用等方面的文献。综上所述,融合基因是脑肿瘤重要的诊断和预测生物标志物。
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Fusion genes as diagnostic and predictive biomarkers for tumor
Structural variants, including chromosomal rearrangements and translocations, may result in the formation of fusion genes. Glioma is the most frequent brain tumor among adults. Due to complex tumor classifications, characterization of recurrence, inadequate sample size and controversial mechanisms of tumor malignancy, clinical strategies have not been developed for almost 30 years. Fusion gene is one of the strong driver events in glioma tumorigenesis and has provided fundamental insights into the disease mechanisms. This review elucidates the literature on the discovery of fusion genes, the development of detection techniques, and their clinical implementations. In conclusion, fusion genes are important diagnostic and predictive biomarkers for brain tumors.
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