RRC ID 44202
著者 Fujimoto D, Hirono Y, Goi T, Katayama K, Matsukawa S, Yamaguchi A.
タイトル The activation of proteinase-activated receptor-1 (PAR1) promotes gastric cancer cell alteration of cellular morphology related to cell motility and invasion.
ジャーナル Int J Oncol
Abstract Cell motility proceeds by cycles of edge protrusion, adhesion and retraction. Whether these functions are coordinated by biochemical or biomechanical processes is unknown. Tumor invasion and metastasis is directly related to cell motility. We showed that stimulation of proteinase-activated receptor-1 (PAR1) can trigger an array of responses that would promote tumor cell growth and invasion. Thus, we examined aspects of PAR1 activation related to cell morphological change that might contribute to cell motility. We established a PAR1 stably transfected MKN45 gastric cancer cell line (MKN45/PAR1). We examined morphological changes, Rho family activation and overexpression of cytoskeletal protein in cells exposed to PAR1 agonists (α-thrombin and TFLLR-NH2). MKN45/PAR1 grows with an elongated and polarized morphology, extending pseudopodia at the leading edge. However, in the presence of PAR1 antagonist, MKN45/PAR1 did not show any changes in cell shape upon addition of either α-thrombin or TFLLR-NH2. Activated PAR1 induced RhoA and Rac1 phosphorylation, and subsequent overexpression of myosin IIA and filamin B which are stress fiber components that were identified by PMF analysis of peptide mass data obtained by MALDI-TOF/MS measurement. Upon stimulation of MKN45/PAR1 for 24 h with either α-thrombin or TFLLR-NH2, the distribution of both myosin IIA and filamin B proteins shifted to being distributed throughout the cytoplasm to the membrane, with more intense luminescence signals than in the absence of stimulation. These results demonstrate that PAR1 activation induces cell morphological change associated with cell motility via Rho family activation and cytoskeletal protein overexpression, and has a critical role in gastric cancer cell invasion and metastasis.
巻・号 42(2)
ページ 565-73
公開日 2013-2-1
DOI 10.3892/ijo.2012.1738
PMID 23242308
MeSH Cell Line, Tumor Cell Movement / genetics* Cytoskeleton / metabolism Filamins / metabolism Gene Expression Regulation, Neoplastic / genetics Humans Neoplasm Invasiveness / genetics* Neoplasm Metastasis / genetics Neoplasm Metastasis / pathology Nonmuscle Myosin Type IIA / metabolism Phosphorylation Receptor, PAR-1 / antagonists & inhibitors Receptor, PAR-1 / genetics Receptor, PAR-1 / metabolism* Stomach Neoplasms / genetics* Stomach Neoplasms / pathology rac1 GTP-Binding Protein / metabolism rhoA GTP-Binding Protein / metabolism
IF 3.899
引用数 12
WOS 分野 ONCOLOGY
リソース情報
ヒト・動物細胞 MKN45(RCB1001) MKN74(RCB1002)