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Multiple Myeloma Genomics – A Concise Review

机译:多发性骨髓瘤基因组学 - 简明审查

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The aim of this review is to summarize the current knowledge of genomic information in multiple myeloma. Multiple myeloma is a genetically complex plasma cell neoplasm that evolves from pre-malignant stages following genomic evolution leading to the proliferation of malignant plasma cells and the production of monoclonal immunoglobulin. The outcomes of patients with myeloma have dramatically improved over the past decade with the introduction of novel agents. Nevertheless, the disease is considered incurable and displays considerable heterogeneity in clinical presentation, course and survival. This heterogeneity can often be traced to cytogenetic abnormalities in the malignant clone. Accordingly, a large body of literature has examined the impact of genomics on myeloma and risk stratification based on cytogenetics has been adopted. In this review, we will focus on the cytogenetics of multiple myeloma and the prognostic significance as well as possible predictive implications. We will briefly review the existing methodologies relevant to myeloma but explore in greater depth the more novel molecular tools as applied to this disease.Conclusion. The field of genomics in multiple myeloma is rapidly evolving however more translational research is needed to accurately use genomic data as a tool of precision medicine.
机译:本综述的目的是总结多种骨髓瘤中基因组信息的目前知识。多发性骨髓瘤是一种遗传复杂的血浆细胞肿瘤,其在基因组进化后从恶性阶段发育出来导致恶性血浆细胞的增殖和单克隆免疫球蛋白的产生。随着新型药剂的引入,过去十年的骨髓瘤患者的结果显着改善。然而,该疾病被认为是可衰种的并且在临床介绍,过程和生存中显示出相当大的异质性。这种异质性通常可以追溯到恶性克隆中的细胞遗传学异常。因此,大量文献已经研究了基因组学对骨髓瘤的影响,并采用了基于细胞遗传学的风险分层。在本综述中,我们将专注于多发性骨髓瘤的细胞遗传学和预测意义以及可能的预测意义。我们将简要审查与骨髓瘤相关的现有方法,但更深入地探索应用于这种疾病的新的分子工具。结论。多发性骨髓瘤的基因组学领域正在快速发展,然而,需要更多的翻译研究来准确使用基因组数据作为精密药物的工具。

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