• 中国科学论文统计源期刊
  • 中国科技核心期刊
  • 美国化学文摘(CA)来源期刊
  • 日本科学技术振兴机构数据库(JST)

临床输血与检验 ›› 2022, Vol. 24 ›› Issue (2): 222-225.DOI: 10.3969/j.issn.1671-2587.2022.02.017

• 临床研究 • 上一篇    下一篇

SENEX基因对急性髓系白血病细胞增殖和凋亡的影响*

王佳, 陶千山, 沈元元, 董毅   

  1. 230601 安徽医科大学第二附属医院血液科
  • 收稿日期:2021-12-15 发布日期:2022-04-12
  • 通讯作者: 董毅,男,主任医师,主要研究方向为肿瘤免疫与免疫治疗方面研究,(E-mail)dongyixx@126.com。
  • 作者简介:王佳(1988-),女,安徽无为人,主治医师,博士,主要从事肿瘤免疫与免疫治疗方面研究,(E-mail)wangjia198@126.com。
  • 基金资助:
    *本课题受国家自然科学基金(No. 81401293); 安徽省重点研究与开发计划项目(No. 202104j07020030)资助

Effect of SENEX on the Proliferation and Apoptosis of AML Cells

WANG Jia, TAO Qian-shan, SHEN Yuan-yuan, et al   

  1. Department of Hematology, the Second Hospital of Anhui Medical University, Anhui, Hefei 230601
  • Received:2021-12-15 Published:2022-04-12

摘要: 目的 探讨SENEX基因对急性髓细胞性白血病(acute myeloid leukemia,AML)细胞增殖和凋亡的影响。方法 选取20例成人初诊AML患者,5例复发AML,17例完全缓解AML以及7例对照的骨髓标本,qPCR检测SENEX基因的表达水平,流式细胞术检测细胞凋亡,CCK8检测细胞增殖。结果 (1)SENEX基因在初诊及复发AML中表达水平升高,且和疾病状态相关;(2)干扰SENEX基因后,NB4细胞的细胞增殖效率下降,凋亡比例上升;(3)IL-35可减弱阿糖胞苷诱导的NB4细胞凋亡比例及SENEX基因上升趋势。结论 SENEX基因可通过直接促进AML细胞增殖和抑制AML细胞的凋亡来参与AML的发生发展。

关键词: 白血病, 急性髓系白血病, SENEX基因

Abstract: Objective To investigate the effect of SENEX on the proliferation and apoptosis of Acute Myeloid Leukemia (AML) cells. Methods 20 adult patients with newly diagnosed AML, 5 relapsed AML, 17 complete remission of AML, and 7 control bone marrow samples were selected. The expression level of SENEX was detected by qPCR, apoptosis was detected by flow cytometry, and cell proliferation was detected by CCK8. Results (1) The expression level of SENEX increased in newly diagnosed and relapsed AML, and was related to the disease status; (2) After sliencing with SENEX, the cell proliferation efficiency of NB4 cells decreased and the proportion of apoptosis increased; (3) IL-35 can attenuate the apoptotic proportion of NB4 cell and the upward trend of SENEX gene induced by cytarabine . Conclusions enex might participate in the occurrence and development of AML by directly promoting the proliferation of AML cells and inhibiting the apoptosis of AML cells.

Key words: Leukemia, Acute myeloid leukemia, SENEX

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