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. 2012 Apr;22(4):310-8.
doi: 10.1097/FPC.0b013e32834f94cb.

Celecoxib pathways: pharmacokinetics and pharmacodynamics

Affiliations

Celecoxib pathways: pharmacokinetics and pharmacodynamics

Li Gong et al. Pharmacogenet Genomics. 2012 Apr.
No abstract available

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Conflict of interest statement

Conflicts of interest

There are no conflicts of interest.

Figures

Fig. 1
Fig. 1
Hepatic metabolism of celecoxib. ADH, alcohol dehydrogenases; UGTs, UDP glucuronosyltransferases. A fully interactive version is available online at http://www.pharmgkb.org/pathway/PA165816736.
Fig. 2
Fig. 2
Stylized cell depicting the mechanism of action of celecoxib and candidate genes interacting with celecoxib and involved in the proposed anticancer mechanisms of celecoxib, including induction of apoptosis, cell cycle arrest, regulation of angiogenesis, and induction of endoplasmic reticulum (ER) stress. CACN: L-type calcium channels; KCNQ: voltage-gated potassium channels; MMP9, metalloproteinase; NSAIDs, nonsteroidal anti-inflammatory drugs; PGH2, prostaglandin H2; PGE2, prostaglandin E2; PGI2, prostacyclin; PGD2, prostaglandin D2; PGF2, prostaglandin F2; PTGER, prostaglandin E receptors; SERCA, sarcoplasmic/ER calcium ATPases; TXA2, thromboxane A2; VEGFA, vascular endothelial cell growth factor. A fully interactive version is available online at http://www.pharmgkb.org/pathway/PA152241951.

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