Results 11 to 20 of about 101,527 (239)

Antimetastatic activity of a cyclooxygenase-2 inhibitor [PDF]

open access: yesBritish Journal of Cancer, 2004
Cyclooxygenase-2 (COX-2) expression is increased in breast cancer and surgery has been shown to increase the growth of metastatic tumours. We investigated the effect of selective COX-2 inhibition on the growth of metastases in either an experimental metastasis model or following excision of a murine primary breast tumour.
Judith H. Harmey   +4 more
openaire   +3 more sources

The relationship between angiogenesis and cyclooxygenase-2 expression in prostate cancer [PDF]

open access: yes, 2005
<b>OBJECTIVE</b>: To test the hypothesis that angiogenesis in prostate cancer is associated with tumour invasion and metastasis, and that this is mediated through increased cyclooxygenase-2 (COX-2) expression.
Bartlett, J.M.S.   +3 more
core   +1 more source

SELECTIVE CYCLOOXYGENASE-2 INHIBITORS

open access: yesRheumatic Disease Clinics of North America, 1999
The identification of COX-2 less than a decade ago has been followed by an unprecedented period of discovery and drug development. An awareness of the existence of two COX isoforms has led to potential novel insights into disease pathogenesis (arthritis, Alzheimer's disease, cancer) and the regulation of normal physiology (brain, kidney).
Brian D. Golden, Steven B. Abramson
openaire   +2 more sources

Meloxicam decreases the migration and invasion of CF41.Mg canine mammary carcinoma cells [PDF]

open access: yes, 2017
Indexación: Web of Science; Scopus.Cyclooxygenase (COX)-2 expression is positively correlated with malignant features in canine mammary carcinomas. Non-steroidal anti-inflammatory drugs (NSAIDs) inhibit COX activity and may therefore possess anticancer ...
Arias, J.I.   +3 more
core   +1 more source

Impact of cyclooxygenase inhibitors in the Women's Health Initiative hormone trials: secondary analysis of a randomized trial. [PDF]

open access: yes, 2006
OBJECTIVES: We evaluated the hypothesis that cyclooxygenase (COX) inhibitor use might have counteracted a beneficial effect of postmenopausal hormone therapy, and account for the absence of cardioprotection in the Women's Health Initiative hormone trials.
Choe, John H   +11 more
core   +3 more sources

Cyclic AMP increases COX-2 expression via mitogen-activated kinase in human myometrial cells [PDF]

open access: yes, 2012
Cyclic AMP (cAMP) is the archetypal smooth muscle relaxant, mediating the effects of many hormones and drugs. However, recently PGI2, acting via cAMP/PKA, was found to increase contraction-associated protein expression in myometrial cells and to promote ...
Amsen   +35 more
core   +2 more sources

Cardiovascular Effects of the Cyclooxygenase Inhibitors [PDF]

open access: yesHypertension, 2007
Cyclooxyenase (COX)-2 selective inhibitors were developed to create a new class of nonsteroidal anti-inflammatory drugs (NSAIDs) with properties similar to those of nonselective NSAIDS but without their potential COX-1–mediated gastrointestinal toxicities.1,2 Studies of the various COX-2 selective inhibitors have shown that they are in fact associated ...
openaire   +3 more sources

Delayed treatment with nimesulide reduces measures of oxidative stress following global ischemic brain injury in gerbils [PDF]

open access: yes, 2003
Metabolism of arachidonic acid by cyclooxygenase is one of the primary sources of reactive oxygen species in the ischemic brain. Neuronal overexpression of cyclooxygenase-2 has recently been shown to contribute to neurodegeneration following ischemic ...
Alvarez, Dalia   +3 more
core   +1 more source

Cyclooxygenase Inhibitors Derived from Thalidomide.

open access: yesChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Kazuo Nagasawa   +6 more
openaire   +4 more sources

Synthesis of 2-Methyl-3-indolylacetic Derivatives as Anti-Inflammatory Agents That Inhibit Preferentially Cyclooxygenase 1 without Gastric Damage [PDF]

open access: yes, 2006
Novel substituted 2-methyl-3-indolylacetic derivatives were synthesized and evaluated for their activity in vitro and in vivo on COX-1 and COX-2. Active compounds were screened to determine their gastrointestinal tolerability in vivo in the rat.
C. Renner   +9 more
core   +1 more source

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