Long non-coding RNA ANGPTL1-3 promotes multiple myeloma bortezomib resistance by sponging miR-30a-3p to activate c-Maf expression

被引:17
|
作者
Nian, Feige [1 ]
Zhu, Jing [2 ]
Chang, Haining [3 ]
机构
[1] Bengbu Med Coll, Sch Clin Med, Bengbu, Anhui, Peoples R China
[2] Bengbu Med Coll, Affiliated Hosp 1, Bengbu, Anhui, Peoples R China
[3] First Peoples Hosp Changzhou, 185 Juqian St, Changzhou 213003, Jiangsu, Peoples R China
关键词
Multiple myeloma; Bortezomib; Lnc-ANGPTL1-3; miR-30a-3p; c-Maf; DRUG-RESISTANCE; PROLIFERATION; FAMILY;
D O I
10.1016/j.bbrc.2019.05.078
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multiple Myeloma (MM) is a malignant hematological disease characterized by monoclonal proliferation of plasma cells in the bone marrow. In recent years, the widespread use of new drugs based on bortezomib (Btz) has significantly improved the remission rate of MM patients. However, drug resistance and disease relapse occur within a few years and MM is still considered to be an incurable disease. The amplification of the long arm of chromosome 1 is one of the most common genetic abnormalities in MM patients. Here, we found that long non-coding RNA ANGPTL1-3 which located in 1q region was over expressed in MM. Lnc-ANGPTL1-3 expression was correlated with MM International Staging System (ISS) and overall survival. Notably, knockdown of Inc-ANGPTL1-3 increased Btz sensitivity of MM cells. Following exploration revealed that Inc-ANGPTL1-3 competitively interacted with miR-30a-3p to c-Maf, a transcription factor which was reported to be associated with Btz resistance. Taken together, our findings demonstrate that Inc-ANGPTL1-3/miR-30a-3p/c-Maf axis plays a critical role in MM Btz resistance. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:1140 / 1146
页数:7
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