High-level expression of cyclooxygenase (COX)-2 is reported in 80 -90% of colorectal adenocarcinomas. Selective inhibition of COX-2 was shown to reduce colorectal tumorigenesis in different models of carcinogenesis and to prevent metastasis in xenograft tumor models, as well as to suppress in vitro
Inhibition of cell proliferation and induction of apoptosis by ExFABP gene targeting
✍ Scribed by Eddi Di Marco; Nadia Sessarego; Barbara Zerega; Ranieri Cancedda; Fiorella Descalzi Cancedda
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 363 KB
- Volume
- 196
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Ex‐FABP, an extracellular fatty acid binding lipocalin, is physiologically expressed by differentiating chicken chondrocytes and myoblasts. Its expression is enhanced after cell treatment with inflammatory stimuli and repressed by anti‐inflammatory agents, behaving as an acute phase protein. Chicken liver fragments in culture show enhanced protein expression after bacterial endotoxin treatment. To investigate the biological role of Ex‐FABP, we stably transfected proliferating chondrocytes with an expression vector carrying antisense oriented Ex‐FABP cDNA. We observed a dramatic loss of cell viability and a strong inhibition of cell proliferation and differentiation. When chondrocytes were transfected with the antisense oriented Ex‐FABP cDNA we observed that Ex‐FABP down‐modulation increased apoptotic cell number. Myoblasts transfected with the same expression vector showed extensive cell death and impaired myotube formation. We suggest that Ex‐FABP acts as a constitutive survival protein and that its expression and activation are fundamental to protect chondrocytes from cell death. J. Cell. Physiol. 196: 464–473, 2003. © 2003 Wiley‐Liss, Inc.
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