Role of Beclin-1-Mediated Autophagy in the Survival of Pediatric Leukemia Cells
Background/Aims: Acute and chronic leukemia are severe malignant cancers worldwide, and can occur in pediatric patients. Since bone marrow cell transplantation is seriously limited by the availability of the immune-paired donor sources, the therapy for pediatric leukemia (PL) remains challenging. Au...
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Cell Physiol Biochem Press GmbH & Co KG
2016-10-01
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doaj-598053e849bd456481768ad2cc9081272020-11-25T01:00:17ZengCell Physiol Biochem Press GmbH & Co KGCellular Physiology and Biochemistry1015-89871421-97782016-10-013951827183610.1159/000447882447882Role of Beclin-1-Mediated Autophagy in the Survival of Pediatric Leukemia CellsXiaoli WuXuefeng FengXiaoqing ZhaoFutian MaNa LiuHongming GuoChaonan LiHuan DuBaoxi ZhangBackground/Aims: Acute and chronic leukemia are severe malignant cancers worldwide, and can occur in pediatric patients. Since bone marrow cell transplantation is seriously limited by the availability of the immune-paired donor sources, the therapy for pediatric leukemia (PL) remains challenging. Autophagy is essential for the regulation of cell survival in the harsh environment. However, the role of autophagy in the survival of PL cells under the oxidative stress, e.g. chemotherapy, remain ill-defined. In the current study, we addressed these questions. Methods: We analyzed the effects of oxidative stress on the cell viability of PL cells in vitro, using a CCK-8 assay. We analyzed the effects of oxidative stress on the apoptosis and autophagy of PL cells. We analyzed the levels of Beclin-1 and microRNA-93 (miR-93) in PL cells. Prediction of binding between miR-93 and 3'-UTR of Beclin-1 mRNA was performed by a bioinformatics algorithm and confirmed by a dual luciferase reporter assay. The relationship between levels of miR-93 and patients' survival was analyzed in PL patients. Results: We found that oxidative stress dose-dependently increased autophagy in PL cells. While low-level oxidative stress did not increase apoptosis, high-level oxidative stress increased apoptosis, seemingly from failure of autophagy-mediated cell survival. High-level oxidative stress appeared to suppress the protein levels of an autophagy protein Beclin-1 in PL cells, possibly through induction of miR-93, which inhibited the translation of Beclin-1 mRNA via 3'-UTR binding. Conclusion: Beclin-1-mediated autophagy plays a key role in the survival of PL cells against oxidative stress. Induction of miR-93 may increase the sensitivity of PL cells to oxidative stress during chemotherapy to improve therapeutic outcome.http://www.karger.com/Article/FullText/447882Pediatric leukemia (PL)Oxidative stressAutophagyApoptosisBeclin-1miR-93 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xiaoli Wu Xuefeng Feng Xiaoqing Zhao Futian Ma Na Liu Hongming Guo Chaonan Li Huan Du Baoxi Zhang |
spellingShingle |
Xiaoli Wu Xuefeng Feng Xiaoqing Zhao Futian Ma Na Liu Hongming Guo Chaonan Li Huan Du Baoxi Zhang Role of Beclin-1-Mediated Autophagy in the Survival of Pediatric Leukemia Cells Cellular Physiology and Biochemistry Pediatric leukemia (PL) Oxidative stress Autophagy Apoptosis Beclin-1 miR-93 |
author_facet |
Xiaoli Wu Xuefeng Feng Xiaoqing Zhao Futian Ma Na Liu Hongming Guo Chaonan Li Huan Du Baoxi Zhang |
author_sort |
Xiaoli Wu |
title |
Role of Beclin-1-Mediated Autophagy in the Survival of Pediatric Leukemia Cells |
title_short |
Role of Beclin-1-Mediated Autophagy in the Survival of Pediatric Leukemia Cells |
title_full |
Role of Beclin-1-Mediated Autophagy in the Survival of Pediatric Leukemia Cells |
title_fullStr |
Role of Beclin-1-Mediated Autophagy in the Survival of Pediatric Leukemia Cells |
title_full_unstemmed |
Role of Beclin-1-Mediated Autophagy in the Survival of Pediatric Leukemia Cells |
title_sort |
role of beclin-1-mediated autophagy in the survival of pediatric leukemia cells |
publisher |
Cell Physiol Biochem Press GmbH & Co KG |
series |
Cellular Physiology and Biochemistry |
issn |
1015-8987 1421-9778 |
publishDate |
2016-10-01 |
description |
Background/Aims: Acute and chronic leukemia are severe malignant cancers worldwide, and can occur in pediatric patients. Since bone marrow cell transplantation is seriously limited by the availability of the immune-paired donor sources, the therapy for pediatric leukemia (PL) remains challenging. Autophagy is essential for the regulation of cell survival in the harsh environment. However, the role of autophagy in the survival of PL cells under the oxidative stress, e.g. chemotherapy, remain ill-defined. In the current study, we addressed these questions. Methods: We analyzed the effects of oxidative stress on the cell viability of PL cells in vitro, using a CCK-8 assay. We analyzed the effects of oxidative stress on the apoptosis and autophagy of PL cells. We analyzed the levels of Beclin-1 and microRNA-93 (miR-93) in PL cells. Prediction of binding between miR-93 and 3'-UTR of Beclin-1 mRNA was performed by a bioinformatics algorithm and confirmed by a dual luciferase reporter assay. The relationship between levels of miR-93 and patients' survival was analyzed in PL patients. Results: We found that oxidative stress dose-dependently increased autophagy in PL cells. While low-level oxidative stress did not increase apoptosis, high-level oxidative stress increased apoptosis, seemingly from failure of autophagy-mediated cell survival. High-level oxidative stress appeared to suppress the protein levels of an autophagy protein Beclin-1 in PL cells, possibly through induction of miR-93, which inhibited the translation of Beclin-1 mRNA via 3'-UTR binding. Conclusion: Beclin-1-mediated autophagy plays a key role in the survival of PL cells against oxidative stress. Induction of miR-93 may increase the sensitivity of PL cells to oxidative stress during chemotherapy to improve therapeutic outcome. |
topic |
Pediatric leukemia (PL) Oxidative stress Autophagy Apoptosis Beclin-1 miR-93 |
url |
http://www.karger.com/Article/FullText/447882 |
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