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Spinster同源基因家族在急性髓系白血病中的预后意义

Prognostic significance of Spinster homolog gene family in acute myeloid leukemia.

作者信息

Huang Wenhui, Qian Tingting, Cheng Zhiheng, Zeng Tiansheng, Si Chaozeng, Liu Chaojun, Deng Cong, Ye Xu, Liu Yan, Cui Longzhen, Fu Lin

机构信息

Department of Hematology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510260, China.

Translational Medicine Center, State Key Laboratory of Respiratory Disease, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, China.

出版信息

J Cancer. 2020 May 18;11(15):4581-4588. doi: 10.7150/jca.44766. eCollection 2020.

Abstract

Acute myeloid leukemia (AML) is a clonal and heterogeneous disease characterized by proliferation of immature myeloid cells, with impaired differentiation and maturation. Spinster homolog (SPNS) is a widely distributed transmembrane transporter, which assists sphingolipids in playing their roles through the cell membrane. However, the expression and clinical implication of the family has not been investigated in AML. From the Cancer Genome Atlas database, a total of 155 AML patients with complete clinical characteristics and expression data were contained in our study. In patients who received chemotherapy only, high expressions of and had adverse effects on event-free survival (EFS) and overall survival (OS) (all <0.05). However, in the allogeneic hematopoietic stem cell transplantation (allo-HSCT) group, we only found a significant difference in OS between the high and low expression groups (=0.001), while other members showed no effect on survival. Multivariate analysis indicated that high expression was an independent risk factor for both EFS and OS in chemotherapy patients. The results confirmed that high expression of and were poor prognostic factors, and the effect of can be neutralized by allo-HSCT.

摘要

急性髓系白血病(AML)是一种克隆性异质性疾病,其特征为未成熟髓系细胞增殖,伴有分化和成熟受损。Spinster同源物(SPNS)是一种广泛分布的跨膜转运蛋白,它协助鞘脂通过细胞膜发挥作用。然而,该家族在AML中的表达及临床意义尚未得到研究。从癌症基因组图谱数据库中,我们的研究纳入了155例具有完整临床特征和表达数据的AML患者。在仅接受化疗的患者中,SPNS2和SPNS3的高表达对无事件生存期(EFS)和总生存期(OS)有不良影响(均P<0.05)。然而,在异基因造血干细胞移植(allo-HSCT)组中,我们仅发现SPNS2高表达组和低表达组之间的OS存在显著差异(P=0.001),而其他SPNS家族成员对生存无影响。多因素分析表明,在化疗患者中,SPNS2高表达是EFS和OS的独立危险因素。结果证实,SPNS2和SPNS3高表达是不良预后因素,且allo-HSCT可抵消SPNS2的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d2e/7255376/3bb9bb224215/jcav11p4581g001.jpg

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