多种血液学恶性肿瘤中CHST9拷贝数变异的研究

Xiaosu Zhao , Qi Wu , Xinrong Fu , Bo Yu , Yong Shao , Hong Yang , Ming Guan , Xiaojun Huang , Wei Zhang , Jun Wan
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引用次数: 11

摘要

碳水化合物n -乙酰半乳糖胺4-0硫转移酶9 (CHST9)属于n -乙酰半乳糖胺4-硫转移酶(GalNAc4ST)家族。最近的一项基于阵列的研究暗示了急性髓性白血病基因组中包含CHST9的区域存在拷贝数变异(CNV)。然而,目前的大多数研究都集中在CNV的全基因组筛选上,这些区域的功能影响需要在大量临床样本中进行广泛的研究。在我们的研究中,我们收集了617例来自多种类型血液恶性肿瘤以及健康对照的骨髓样本,并通过实时聚合酶链反应(PCR)检测CHST9的CNV。我们发现CHST9的CNV与这些血液系统恶性肿瘤包括急性淋巴细胞白血病、急性髓性白血病、慢性淋巴细胞白血病、慢性髓性白血病、多发性骨髓瘤和骨髓增生异常综合征之间存在显著关联。我们还检测了CHST9 mRNA在DNA有一个或两个拷贝的样品中的表达,发现相对表达水平与基因剂量之间存在弱而正的相关性。总的来说,CHST9的CNV已被证明与血液系统恶性肿瘤有关。然而,CNV的功能后果需要在未来进行广泛的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Examination of copy number variations of CHST9 in multiple types of hematologic malignancies

Carbohydrate N-acetylgalactosamine 4-0 sulfotransferase 9 (CHST9) belongs to the N-acetylgalactosamine 4-sulfotransferase (GalNAc4ST) family. A recent array-based study implicated the presence of copy-number variations (CNV) of the region encompassing CHST9 in the genomes of acute myelogenous leukemia. Most of the current studies, however, focused on the genome-wide screening of CNV, and the functional impact of such regions needs to be extensively investigated in large amounts of clinical samples. In our study, we collected 617 bone marrow samples from multi-types of hematologic malignancies, as well as healthy controls, and detected the CNV of CHST9 by real-time polymerase chain reaction (PCR). We found significant association between the CNV of CHST9 and these hematologic malignancies including acute lymphoblastic leukemia, acute myelogenous leukemia, chronic lymphocytic leukemia, chronic myelogenous leukemia, multiple myeloma, and myelodysplastic syndrome. We also examined CHST9 mRNA expression in the samples with one or two copies of DNA, and observed a weak yet positive correlation between the relative expression level and gene dosage. In general, the CNV of CHST9 have been shown to associate with hematologic malignancies. The functional consequences of CNV, however, need to be investigated extensively in the future.

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