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Celecoxib Inhibits Urokinase-Type Plasminogen Activator (uPA) Production in MDA-MB-231 Breast Cancer Cells

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Summary

Elevated urokinase-type plasminogen activator (uPA) expression in breast tumors predicts poor survival. We found celecoxib (25 μM) significantly reduced uPA protein and mRNA in MDA-MB-231 breast cancer cells following 72 h of treatment. Celecoxib also inhibited cell viability (12.5 and 25 μM) and induced G2M arrest (25 μM). Therefore, celecoxib therapy for uPA positive breast cancer should be explored.

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Abbreviations

COX-2:

cyclo-oxygenase II

ELISA:

enzyme linked immunosorbent assay

Erk 1/2:

extra-cellular regulated kinase 1 and 2

IGF-I:

insulin-like growth factor I

IGF-IR:

IGF-I receptor

MAPK I:

mitogen-activated protein kinase I

MTS:

3-(4,5 dimethylthiazol-2-yl)-5-(3 carboxymethoxyphenyl)-2-(4 sulfophenyl)-2H-tetrazolium

NSAID:

nonsteroidal anti-inflammatory drug, PI3K phosphatidyl-inositol 3 kinase

qRT-PCR:

quantitative real time polymerase chain reaction

TBP:

TATA box binding protein

TGF-beta:

transforming growth factor-beta

uPA:

urokinase-type plasminogen activator

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Correspondence to Sandra E. Dunn.

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Andrews, H.N., Habibi, G., Kucab, J.E. et al. Celecoxib Inhibits Urokinase-Type Plasminogen Activator (uPA) Production in MDA-MB-231 Breast Cancer Cells. Breast Cancer Res Treat 94, 47–52 (2005). https://doi.org/10.1007/s10549-005-6941-5

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