已发表论文

LINC00096 通过海绵化 miR-383-5p 和调节三阴性乳腺癌中的 RBM3 表达来促进其增殖和侵袭

 

Authors Tian Y, Xia S, Ma M, Zuo Y

Received 3 September 2019

Accepted for publication 21 November 2019

Published 2 December 2019 Volume 2019:12 Pages 10569—10578

DOI https://doi.org/10.2147/OTT.S229659

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Mr Uzwal Prakash

Peer reviewer comments 2

Editor who approved publication: Prof. Dr. Geoffrey Pietersz

Background: Recent studies revealed that long non-coding RNAs (lncRNA) play crucial roles in cancer initiation and progression. However, the function and underlying mechanism of lncRNAs in triple-negative breast cancer (TNBC) are little investigated.
Methods: qRT-PCR was used to investigate LINC00096 expression in TNBC tissues and cells. Function assays were used to test the effects of LINC00096 on TNBC cells progression. In addition, luciferase reporter and qRT-PCR assays were used to determine the underlying mechanism of LINC00096 on TNBC progression.
Results: In our present study, we identify LINC00096 as one of the most upregulated lncRNA in TNBC progression by using microarray screening. High LINC00096 expression was obviously related to advanced tumor stage, metastasis, poor prognosis of patients. Loss-of-function assays showed that LINC00096 suppression reduced TNBC cells proliferation and invasive abilities in vitro. Mechanistically, we demonstrated that LINC00096 directly interacted with miR-383-5p, subsequently acted as a miRNA sponge to increase RBM3 expression.
Conclusion: In the present study, we indicated that LINC00096 might promote the proliferation and invasion through regulating the miR-383-5p/RBM3 pathway in TNBC, which providing a novel therapeutic target for cancer treatment.
Keywords: LINC00096, miR-383-5p, RBM3, triple-negative breast cancer




Figure 2 LINC00096 was upregulated in TNBC...