| Literature DB >> 27272788 |
Masanori Masui1, Tatsuo Okui1, Tsuyoshi Shimo2, Kiyofumi Takabatake3, Takuya Fukazawa4, Kenichi Matsumoto1, Naito Kurio1, Soichiro Ibaragi1, Yoshio Naomoto4, Hitoshi Nagatsuka3, Akira Sasaki1.
Abstract
Midkine is a heparin-binding growth factor highly expressed in various human malignant tumors. However, its role in the growth of oral squamous cell carcinoma is not well understood. In this study, we analyzed the antitumor effect of a novel midkine inhibitor (iMDK) against oral squamous cell carcinoma. Administration of iMDK induced a robust antitumor response and suppressed cluster of differentiation 31 (CD31) expression in oral squamous cell carcinoma HSC-2 cells and SAS cells xenograft models. iMDK inhibited the proliferation of these cells dose-dependently, as well as the expression of midkine and phospho-extracellular signal-regulated kinase in HSC-2 and SAS cells. Moreover, iMDK significantly inhibited vascular endothelial growth factor and induced tube growth of human umbilical vein endothelial cells in a dose-dependent fashion. These findings suggest that midkine is critically involved in oral squamous cell carcinoma and iMDK can be effectively used for the treatment of oral squamous cell carcinoma. CopyrightEntities:
Keywords: Midkine; angiogenesis; iMDK; oral squamous cell carcinoma
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Year: 2016 PMID: 27272788
Source DB: PubMed Journal: Anticancer Res ISSN: 0250-7005 Impact factor: 2.480