Transforming growth factor-β transiently induces vimentin expression and invasive capacity in a canine mammary gland tumor cell line

被引:15
|
作者
Yoshida, K. [1 ]
Saito, T. [1 ]
Kamida, A. [1 ]
Matsumoto, K. [1 ]
Saeki, K. [1 ]
Mochizuki, M. [1 ]
Sasaki, N. [1 ]
Nakagawa, T. [1 ]
机构
[1] Univ Tokyo, Lab Vet Surg, Grad Sch Agr & Life Sci, Tokyo 1138657, Japan
关键词
Dog; Mammary gland tumor; EMT; TGF-beta; MET; xCELLigence RTCA; EPITHELIAL-MESENCHYMAL TRANSITIONS; TGF-BETA; IN-VITRO; PROGRESSION; NEOPLASMS; CANCER;
D O I
10.1016/j.rvsc.2012.10.016
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The epithelial-mesenchymal transition (EMT) is a crucial event that occurs during cancer metastasis and can be induced by transforming growth factor-beta (TGF-beta) in various tumor cells in vitro. However, little is known about the effects of TGF-beta in canine mammary gland tumors (CMGTs). Here, we investigated the role of TGF-beta in CMGT. We observed that treatment of the CMGT cell line CHMp13a with TGF-beta 1 leads to transient induction of the mesenchymal marker vimentin. Real-time measurements of cellular electrical impedance also showed that CMGT invasiveness is transiently increased by TGF-beta 1 treatment, but is reversed after prolonged stimulation. This phenomenon is similar to the mesenchymal-epithelial transition (MET, the reverse phenomenon of EMT), and a process that is implicated in the establishment of secondary metastatic lesions. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:539 / 541
页数:3
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