| Literature DB >> 32819585 |
Tatsuya Yoshida1, Nobuyasu Suganuma1, Shinya Sato2, Soji Toda3, Hirotaka Nakayama4, Katsuhiko Masudo5, Yoichiro Okubo6, Hiroyuki Hayashi7, Tomoyuki Yokose6, Naohiko Koshikawa8, Yasushi Rino9, Hiroyuki Iwasaki3, Yohei Miyagi2, Munetaka Masuda9, Daisuke Hoshino10.
Abstract
Anaplastic thyroid carcinoma (ATC) is one of the most aggressive cancer types; however, the molecular mechanism contributing to the aggressive characteristics remain unclear. Membrane type 1 matrix metalloproteinase (MT1-MMP) plays an important role in cancer invasion and has been associated with a poor prognosis in various malignant neoplasms. In this study, we investigated the relationship between MT1-MMP expression and the proliferation and invasion of ATC cells, along with the association with clinicopathologic factors in patients with ATC. Suppression of MT1-MMP reduced the proliferation and invasion of ATC cells, and suppressed ERK activity, indicating a role in cancer cell proliferation in collagen matrix culture conditions. The expression of MT1-MMP was detected in 29 of 34 (85.3%) surgical specimens from ATC patients. In addition, the expression of MT1-MMP in the tumor lesion was higher than that of normal and stromal tissues. Collectively, these results suggest that elevated MT1-MMP expression plays a role in the pathogenesis of ATC, which may promote its aggressive characteristics such as proliferation and invasion, highlighting a potential new therapeutic target.Entities:
Keywords: 3D culture; Anaplastic thyroid cancer; Collagen; Immunohistochemistry; Invasion; MT1-MMP
Year: 2020 PMID: 32819585 DOI: 10.1016/j.bbrc.2020.06.043
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575