科研成果详情

题名Synergistic apoptosis induction in leukemic cells by miR-15a/16-1 and arsenic trioxide
作者
发表日期2010-12-10
发表期刊BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS   影响因子和分区
语种英语
原始文献类型Article
关键词Arsenic trioxide MiR-15a/16-1 Apoptosis Leukemia
其他关键词ACUTE PROMYELOCYTIC LEUKEMIA ; CHRONIC MYELOID-LEUKEMIA ; DOWN-REGULATION ; BCR-ABL ; CANCER ; MICRORNAS ; MIR-16-1 ; EXPRESSION ; RESISTANCE ; IMATINIB
摘要MicroRNAs (miRNAs) are small noncoding RNAs that regulate target gene expression through translation repression or messenger RNA degradation. MiR-15a and 16-1 form a cluster at the chromosomal region 13q14, which is frequently deleted or down-regulated in chronic lymphocytic leukemia. Arsenic trioxide (As2O3, ATO) has been successfully applied to treat acute promyelocytic leukemia (APL). Its combination with other drugs presented therapeutic activities in hematologic and solid tumors. Here we investigated the potential synergy between miR-15a/16-1 and ATO on Bcr-Abl positive leukemic K562 cells. In this study, we found that combination of miR-15a/16-1 and ATO synergistically induced growth inhibition and apoptosis in K562 cells. The apoptosis, at least in part, through regulating mitochondrial function including the release of cytochrome c and loss of mitochondrial transmembrane potential, also activation of caspase-3 and degradation of poly-adenosine diphosphate-ribose polymerase. However, the expression of Bcr-Abl was not affected by ATO and/or miR-15a/16-1. Moreover, apoptotic synergy between miR-15a/16-1 and ATO was observed in Bcr-Abl negative leukemic cell lines and primary leukemic cells. Taken together, these findings suggested that the combined regiment of miR-15a/16-1 and ATO might be a potential therapeutic remedy for the treatment of leukemia. (C) 2010 Elsevier Inc. All rights reserved.
出版者ACADEMIC PRESS INC ELSEVIER SCIENCE
出版地SAN DIEGO
ISSN0006-291X
EISSN1090-2104
卷号403期号:2页码:203-208
DOI10.1016/j.bbrc.2010.10.137
页数6
WOS类目Biochemistry & Molecular Biology ; Biophysics
WOS研究方向Biochemistry & Molecular Biology ; Biophysics
WOS记录号WOS:000285534500009
收录类别SCIE ; PUBMED ; SCOPUS
URL查看原文
PubMed ID21056550
SCOPUSEID2-s2.0-78649905889
通讯作者地址[Jiang, Lei]Affiliated Hosp 1, Lab Internal Med, Wenzhou Med Coll, Wenzhou 325000, Zhejiang, Peoples R China.
引用统计
被引频次:26[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符https://kms.wmu.edu.cn/handle/3ETUA0LF/15614
专题附属第一医院_内科实验室
附属第一医院_血液内科
通讯作者Jiang, Lei
作者单位
1.Affiliated Hosp 1, Lab Internal Med, Wenzhou Med Coll, Wenzhou 325000, Zhejiang, Peoples R China;
2.Affiliated Hosp 1, Dept Hematol, Wenzhou Med Coll, Wenzhou 325000, Zhejiang, Peoples R China;
3.Wenzhou Med Coll, Inst Hematol & Immunol, Wenzhou 325000, Zhejiang, Peoples R China
第一作者单位附属第一医院;  内科实验室
通讯作者单位附属第一医院;  内科实验室
第一作者的第一单位附属第一医院
推荐引用方式
GB/T 7714
Gao, Shen-meng,Chen, Chiqi,Wu, Jianbo,et al. Synergistic apoptosis induction in leukemic cells by miR-15a/16-1 and arsenic trioxide[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,2010,403(2):203-208.
APA Gao, Shen-meng., Chen, Chiqi., Wu, Jianbo., Tan, Yanxia., Yu, Kang., ... & Jiang, Lei. (2010). Synergistic apoptosis induction in leukemic cells by miR-15a/16-1 and arsenic trioxide. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 403(2), 203-208.
MLA Gao, Shen-meng,et al."Synergistic apoptosis induction in leukemic cells by miR-15a/16-1 and arsenic trioxide".BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 403.2(2010):203-208.

条目包含的文件

条目无相关文件。
个性服务
查看访问统计
谷歌学术
谷歌学术中相似的文章
[Gao, Shen-meng]的文章
[Chen, Chiqi]的文章
[Wu, Jianbo]的文章
百度学术
百度学术中相似的文章
[Gao, Shen-meng]的文章
[Chen, Chiqi]的文章
[Wu, Jianbo]的文章
必应学术
必应学术中相似的文章
[Gao, Shen-meng]的文章
[Chen, Chiqi]的文章
[Wu, Jianbo]的文章
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。