Song Qibin, Peng Min, Chu Yuxin, Huang Shiang
Cancer Center, Renmin Hospital of Wuhan University, Wuhan, China.
Molecular department, Kindstar Global, Wuhan, China.
Oncotarget. 2017 May 9;8(37):62716-62729. doi: 10.18632/oncotarget.17698. eCollection 2017 Sep 22.
Myelodysplastic syndromes (MDS) are a group of heterogeneous hematologic diseases. Chromosomal aberrations are important for the initiation, development, and progression of MDS. Detection of chromosomal abnormalities in MDS is important for categorization, risk stratification, therapeutic selection, and prognosis evaluation of the disease. Recent progress of multiple techniques has brought powerful molecular cytogenetic information to reveal copy number variation, uniparental disomy, and complex chromosomal aberrations in MDS. In this review, we will introduce some common chromosomal aberrations in MDS and their clinical significance. Then we will explain the application, advantages, and limitations of different techniques for detecting chromosomal abnormalities in MDS. The information in this review may be helpful for clinicians to select appropriate methods in patient-related decision making.
骨髓增生异常综合征(MDS)是一组异质性血液系统疾病。染色体畸变对MDS的起始、发展和进展至关重要。检测MDS中的染色体异常对于该疾病的分类、风险分层、治疗选择和预后评估具有重要意义。多种技术的最新进展带来了强大的分子细胞遗传学信息,以揭示MDS中的拷贝数变异、单亲二体和复杂染色体畸变。在本综述中,我们将介绍MDS中一些常见的染色体畸变及其临床意义。然后我们将解释检测MDS中染色体异常的不同技术的应用、优点和局限性。本综述中的信息可能有助于临床医生在与患者相关的决策中选择合适的方法。