论文已发表
注册即可获取德孚的最新动态
IF 收录期刊
Authors Xie X, Xiao Y, Huang X
Received 7 June 2017
Accepted for publication 3 August 2017
Published 22 January 2018 Volume 2018:11 Pages 473—482
DOI https://doi.org/10.2147/OTT.S143440
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Colin Mak
Peer reviewer comments 2
Editor who approved publication: Dr Samir Farghaly
Aim: Homeobox (HOX) genes and their protein products have been found to
function as oncogenes in the progression of many cancers. But the role of
Homeobox C10 (HOXC10) in osteosarcoma (OS) still remains less understood. In
this study, we firstly determine the biologic functions of HOXC10 in OS.
Materials and methods: We examined the expression of HOXC10 in OS
tissues by quantitative real-time polymerase chain reaction and Western
blot assays. We investigated the effects of HOXC10 on cell proliferation,
apoptosis and caspase 3 activity in three OS cell lines by RNA interference,
Cell Counting Kit-8, flow cytometry and colorimetric assays.
Results: We found that HOXC10 was elevated in OS tissues.
Silencing HOXC10 significantly inhibited cell proliferation, induced cell apoptosis
and increased the expression and activity of caspase 3. The resistance assay
further suggested that HOXC10 affected cell growth and apoptosis through
regulating the expression and activity of caspase 3.
Conclusion: HOXC10 might function as an oncogene in OS by
regulating the expression and activity of caspase 3.
Keywords: apoptosis,
caspase 3, HOXC10, osteosarcoma, proliferation
