The Effect of Telomerase Inhibition on NK Cell Activity in Acute Myeloid Leukemia.

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Khadijeh Dizaji Asl, Ali Rafat, Ali Akbar Movassaghpour, Hojjatollah Nozad Charoudeh, Hamid Tayefi Nasrabadi
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引用次数: 6

Abstract

Purpose: Acute myeloid leukemia (AML) is known to be an invasive and highly lethal hematological malignancy in adults and children. Resistance to the present treatments, including radiotherapy and chemotherapy with their side effects and telomere length shortening are the main cause of the mortality in AML patients. Telomeres sequence which are located at the end of eukaryotic chromosome play pivotal role in genomic stability. Recent studies have shown that apoptosis process is blocked in AML patient by the excessive telomerase activity in cancerous blasts. Therefore, the find of effective ways to prevent disease progression has been considered by the researchers. Natural killer (NK) cells as granular effector cells play a critical role in elimination of abnormal and tumor cells. Given that the cytotoxic function of NK cells is disrupted in the AML patients, we investigated the effect of telomerase inhibitors on NK cell differentiation. Methods: To evaluate telomerase inhibition on NK cell differentiation, the expression of CD105, CD56, CD57, and KIRs was evaluated in CD34+ derived NK cells after incubation of them with BIBR1532. Results: The results showed that the expression of CD105, CD56, CD57, and KIRs receptors reduces after telomerase inhibition. According to these findings, BIBR1532 affected the final differentiation of NK cells. Conclusion: The results revealed that telomerase inhibitor drugs suppress cancer cell progression in a NK cells-independent process.

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端粒酶抑制对急性髓系白血病NK细胞活性的影响。
目的:急性髓性白血病(AML)是一种侵袭性和高致命性的血液系统恶性肿瘤,适用于成人和儿童。目前的治疗方法,包括放疗和化疗的耐药性及其副作用和端粒缩短是AML患者死亡的主要原因。端粒序列位于真核生物染色体末端,对基因组的稳定性起着至关重要的作用。最近的研究表明,AML患者的细胞凋亡过程被癌性细胞中过度的端粒酶活性所阻断。因此,寻找有效的预防疾病进展的方法已被研究人员所考虑。NK细胞作为颗粒效应细胞,在异常细胞和肿瘤细胞的清除中起着至关重要的作用。鉴于AML患者NK细胞的细胞毒功能被破坏,我们研究了端粒酶抑制剂对NK细胞分化的影响。方法:为了评估端粒酶对NK细胞分化的抑制作用,在CD34+ NK细胞中,BIBR1532孵育后,检测CD105、CD56、CD57和KIRs的表达。结果:端粒酶抑制后,CD105、CD56、CD57和KIRs受体表达降低。根据这些发现,BIBR1532影响NK细胞的最终分化。结论:端粒酶抑制剂对肿瘤细胞的抑制作用与NK细胞无关。
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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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