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HA-1077 inhibits cell migration/invasion of oral squamous cell carcinoma

Authors :
Moreira Carboni, Simone de Sales Costa
Rodrigues Lima, Nathália Alves
Pinheiro, Nanci Mendes
Tavares-Murta, Beatriz Martins
Crema, Virgínia Oliveira
Source :
Anti-Cancer Drugs; October 2015, Vol. 26 Issue: 9 p923-930, 8p
Publication Year :
2015

Abstract

Oral squamous cell carcinoma (OSCC) is the most malignant lesion occurring in the head and neck. The Rho-kinases (ROCKs), effectors of Rho proteins, are involved in actin cytoskeletal organization, cell migration, and maintenance cortex. The HA-1077 inhibits the ROCKs. This study aimed to evaluate the effect of treatment with HA-1077 on cell motility in SCC-4 cells, a cell line originating from human OSCC. F-actin of SCC-4 cells treated or not with HA-1077 (1, 50 and 100 μmol/l), and also HA-1077 50 μmol/l and/or inhibitors Y-27632 30 μmol/l was stained with rhodamine-conjugated phalloidin and analyzed by confocal microscopy. Approximately 1×105 cells/well, control and treated with HA-1077 (25, 50, and 100 μmol/l) were added to the migration plate assay. In addition, 1×105 cells/well, control and treated with HA-1077 50 μmol/l, were tested by invasion assays (plate coated with Matrigel). The inhibition of ROCKs with HA-1077 and/or Y-27632 leads to morphological changes, affecting the organization of the actin. The inhibitory effect of HA-1077 (P<0.0001) was dose dependent as the number of cells migrated at 100 μmol/l was statistically different: 25 μmol/l (P<0.0001) and 50 μmol/l (P<0.01). The number of cells treated with HA-1077 50 μmol/l decreased compared with control cells that invaded through Matrigel (P<0.0001). This study shows an inhibitory effect of HA-1077 on cell migration and invasion, suggesting that the use of HA-1077 can be a potential therapy for OSCC.

Details

Language :
English
ISSN :
09594973 and 14735741
Volume :
26
Issue :
9
Database :
Supplemental Index
Journal :
Anti-Cancer Drugs
Publication Type :
Periodical
Accession number :
ejs48602407
Full Text :
https://doi.org/10.1097/CAD.0000000000000267