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白血病细胞凋亡和自噬对急性髓系白血病患者结局的意义。

Significance of apoptosis and autophagy of leukemic blasts for the outcomes of acute myeloid leukemia patients.

机构信息

Department of Hematology, Blood Cancers and Bone Marrow Transplantation, University Hospital No. 1, Wrocław, Poland.

出版信息

Adv Clin Exp Med. 2019 Jul;28(7):861-869. doi: 10.17219/acem/93849.

Abstract

BACKGROUND

Cytostatic treatment induces apoptosis or other types of cell death like autophagy, necrosis, mitotic catastrophe, etc. Autophagy can play a role in the drug resistance of neoplastic cells, allowing the survival of blast cells under stressful conditions, such as the use of cytostatics. Studies on apoptosis and autophagy 12-24 h after the start of treatment have not been conducted until now.

OBJECTIVES

The study aimed to investigate the predictive and prognostic significance of autophagy and apoptosis in patients with acute myeloid leukemia (AML).

MATERIAL AND METHODS

The study included 38 patients. Blood was collected before and 12-24 h after the start of treatment, since at that time point, the appropriate blast cell count was still available. Autophagy was measured with the expression of the ATG5, MAP1L3, LC3-I, and LC3-II proteins. The percentage of mononuclear cells in early and late apoptosis was evaluated with flow cytometry, using the annexin V and propidium iodide (PI) binding assay.

RESULTS

The percentage of apoptotic blast cells before treatment was not associated with the response. However, in the remission group, the overall percentage of apoptotic cells measured 12-24 h after the start of treatment was higher than in non-remission patients, which was statistically significant. In neither group we found any difference in the level of autophagy before and 12-24 h after the start of treatment. Nevertheless, we observed an increasing tendency of the MAP1LC3 protein expression (not statistically significant) in the remission group 12-24 h after the start of treatment. Patients with a higher percentage of blast cells in apoptosis and with a higher expression of MAP1LC3 protein measured 12-24 h after the start of the therapy had longer overall survival (OS).

CONCLUSIONS

A higher percentage of apoptotic as well as autophagic blast cells measured 12-24 h after the start of the chemotherapy is an independent factor associated with better outcomes.

摘要

背景

细胞抑制剂治疗会诱导细胞凋亡或其他类型的细胞死亡,如自噬、坏死、有丝分裂灾难等。自噬在肿瘤细胞的耐药性中可能发挥作用,使细胞在应激条件下(如细胞抑制剂治疗)下存活。目前为止,还没有研究在治疗开始后 12-24 小时内进行细胞凋亡和自噬的研究。

目的

本研究旨在探讨自噬和细胞凋亡在急性髓系白血病(AML)患者中的预测和预后意义。

材料与方法

本研究共纳入 38 例患者。在治疗开始前和开始后 12-24 小时采集血液,因为此时仍能获得适当的原始细胞计数。自噬通过 ATG5、MAP1L3、LC3-I 和 LC3-II 蛋白的表达来测量。使用 annexin V 和碘化丙啶(PI)结合试验通过流式细胞术评估单核细胞早期和晚期凋亡的百分比。

结果

治疗前原始细胞凋亡的百分比与反应无关。然而,在缓解组中,治疗开始后 12-24 小时测量的总凋亡细胞百分比高于未缓解患者,具有统计学意义。在两组中,我们都没有发现治疗开始前和 12-24 小时后自噬水平的差异。尽管如此,我们观察到治疗开始后 12-24 小时缓解组中 MAP1LC3 蛋白表达有增加的趋势(无统计学意义)。治疗开始后 12-24 小时测量的原始细胞凋亡和 MAP1LC3 蛋白表达较高的患者总生存时间(OS)更长。

结论

化疗开始后 12-24 小时测量的凋亡和自噬原始细胞的百分比较高是与更好的结果相关的独立因素。

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