Alterations in cellular adhesion and apoptosis in epithelial cells overexpressing prostaglandin endoperoxide synthase 2

Article Abstract:

The overexpression of cyclooxegenase (COX) 2 leads to alterations in cell adhesion and prevention of apoptosis. Rat intestinal epithelial cells exhibit resistance to apoptosis induced by butyrate. Sulindac sulfide, a suppressor of COX 2, reverses the effect indicating that COX 2 stimulates tumorigenesis. The expression of COX 2 is elevated in colorectal carcinoma in humans which is reducible by nonsteroidal anti-inflammatory drugs such as aspirin. A better understanding of the molecular mechanisms of COX 2 action will help in the development of drugs to prevent cancers.

author: DuBois, Raymond N., Tsujii, Masahiko
Physiological aspects, Nonsteroidal anti-inflammatory drugs, Nonsteroidal anti-inflammatory agents

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Prostaglandin synthase 1 gene disruption in mice reduces arachidonic acid-induced inflammation and indomethacin-induced gastric ulceration

Article Abstract:

Mice lacking cyclooxegenase (COX) 1 are more healthy and less prone to indomethacin-induced stomach ulcers than the wild-type mice. The homozygous mutant mice exhibit a decrease in platelet aggregation and a reduction in inflammatory responses to archadionic acid. COX 1 and 2 are essential enzymes in prostaglandin synthesis. Female mice with mutations in the gene encoding COX 1 produce few live young ones when mated with homozygous mutant males.

author: Smithies, Oliver, Morham, Scott G., Kim, H.S., Loftin, Charles D., Tiano, Howard F., Mahler, Joel F., Kluckman, Kimberley D., Lee, Christopher A., Langebach, Robert, Ghanayem, Burhan I., Chulada, Patricia C., Goulding, Eugenia H.
Prostaglandins, Prostaglandin synthesis

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Prostaglandin synthase 2 gene disruption causes severe renal pathology in the mouse

Article Abstract:

The absence of the prostaglandin endoperoxide H synthase isoform 2, cyclooxegenase 2 (COX-2), causes abnormalities in the kidney that increase with age. A study conducted on mice with mutations in COX-2 indicates no difference from the wild-type animals in the gastrointestinal pathology. Mutations in the COX-1 gene fail to show any abnormality but the female homozygotes give birth to few live young ones when mated with the males.

author: Smithies, Oliver, Morham, Scott G., Jennette, J. Charles, Langenbach, Robert, Loftin, Charles D., Tiano, Howard F., Vouloumanos, Nectarios, Mahler, Joel F., Kluckman, Kimberley D., Ledford, Aric, Lee, Christopher A.
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subjects list: Observations, Mice, Mice (Rodents), Gene expression, Animal mutation
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