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Novel Suppressive Effects of Ketotifen on Migration and Invasion of MDA-MB-231 and HT-1080 Cancer Cells
Biomolecules & Therapeutics ; : 540-546, 2014.
Article in English | WPRIM | ID: wpr-185389
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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Full text: Available Index: WPRIM (Western Pacific) Main subject: Breast Neoplasms / Cell Movement / Blotting, Western / Mortality / Matrix Metalloproteinase 9 / Extracellular Matrix / Fibrosarcoma / Ketotifen / Neoplasm Metastasis Type of study: Prognostic study Language: English Journal: Biomolecules & Therapeutics Year: 2014 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Breast Neoplasms / Cell Movement / Blotting, Western / Mortality / Matrix Metalloproteinase 9 / Extracellular Matrix / Fibrosarcoma / Ketotifen / Neoplasm Metastasis Type of study: Prognostic study Language: English Journal: Biomolecules & Therapeutics Year: 2014 Type: Article