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Xia, Yang; Xiao, Xiangqian; Deng, Xiongwei; Zhang, Fang; Zhang, Xiaofei; Hu, Qin; Sheng, Wang, E-mail: hq07616@bjut.edu.cn, E-mail: shengwang@bjut.edu.cn2017
AbstractAbstract
[en] Long non-coding RNAs (lncRNAs) are defined as a class of RNA transcripts longer than 200 nucleotides encoded by mammalian genomes that lack protein-coding potential. LncRNA ASBEL has been identified as an anti-sense transcript of BTG3 (B cell translocation gene 3) gene, which encodes an anti-proliferation protein. Remarkable down-regulation of BTG3 has been reported in triple-negative breast cancer (TNBC). In the present study, a number of single-stranded modified anti-sense DNA oligonucleotides (antago) were designed, synthesized and screened for specific lncRNA ASBEL knockdown. We showed here that anti-ASBEL antago played a significant tumor suppressive role in TNBC by effective down-regulating lncRNA ASBEL, which in turn led to increased BTG3 expression. The obtained data suggest lncRNA ASBEL as a novel therapeutic target in TNBC. - Highlights: • LncRNA ASBEL is a promising therapeutic target in TNBC. • Antago is more powerful than siRNA in modulating lncRNA. • Antago3 is a useful therapeutic tool for TNBC treatment.
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S0006-291X(17)31029-X; Available from http://dx.doi.org/10.1016/j.bbrc.2017.05.136; Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Biochemical and Biophysical Research Communications; ISSN 0006-291X;
; CODEN BBRCA9; v. 489(4); p. 386-392

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