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Novel Suppressive Effects of Ketotifen on Migration and Invasion of MDA-MB-231 and HT-1080 Cancer Cellsopen access

Authors
Kim, Hyun JiPark, Mi KyungKim, Soo YoulLee, Chang Hoon
Issue Date
30-Nov-2014
Publisher
KOREAN SOC APPLIED PHARMACOLOGY
Keywords
Ketotifen; Migration; Invasion; MDA-MB-231; HT-1080
Citation
BIOMOLECULES & THERAPEUTICS, v.22, no.6, pp 540 - 546
Pages
7
Indexed
SCIE
SCOPUS
KCI
Journal Title
BIOMOLECULES & THERAPEUTICS
Volume
22
Number
6
Start Page
540
End Page
546
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/15250
DOI
10.4062/biomolther.2014.081
ISSN
1976-9148
2005-4483
Abstract
The high mortality rates associated with cancer reflect the metastatic spread of tumor cells from the site of their origin. Metastasis, in fact, is the cause of 90% of cancer deaths. Therefore, considerable effort is being made to inhibit metastasis. In the present study, we screened ketotifen for anti-migratory and anti-invasive activities against MDA-MB-231 breast cancer and HT-1080 fibrosarcoma cancer cells. Cancer cell migration and invasion were measured using multi-well chambers. Additionally, western blots were used to examine the effects of ketotifen on the expressions of CDC42, Rho, Rac, and matrix metalloproteinase 9 (MMP-9). The results showed that ketotifen dose-dependently suppressed the migration and invasion of MDA-MB-231 and HT-1080 cells. Ketotifen also suppressed the expressions of CDC42, Rac, and Rho, which, significantly, are involved in MDA-MB-231 and HT-1080 cancer cell migration. Moreover, ketotifen suppressed the expression and activity of MMP-9, which is involved in degradation of the extracellular matrix leading to invasion. The overall data suggested that ketotifen suppresses the migration and invasion of MDA-MB-231 and HT-1080 cancer cells via inhibition of CDC42, Rac, Rho, and MMP-9 expression.
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