Zhang, Guang-Sen
Antitumor effects of celecoxib on K562 leukemia cells are mediated by cell-cycle arrest, caspase-3 activation, and downregulation of Cox-2 expression and are synergistic with hydroxyurea or imatinib. [electronic resource]
- American journal of hematology Apr 2006
- 242-55 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
ISSN: 0361-8609
Standard No.: 10.1002/ajh.20542 doi
Subjects--Topical Terms: Antineoplastic Agents--pharmacology Antineoplastic Combined Chemotherapy Protocols--pharmacology Apoptosis--drug effects Benzamides Bone Marrow Cells--enzymology Caspase 3 Caspase Inhibitors Caspases--metabolism Celecoxib Cyclin D1--metabolism Cyclin E--metabolism Cyclin-Dependent Kinase Inhibitor p16--metabolism Cyclin-Dependent Kinase Inhibitor p27 Cyclooxygenase 2--biosynthesis Cyclooxygenase Inhibitors--pharmacology Dose-Response Relationship, Drug Down-Regulation--drug effects Drug Synergism Enzyme Activation--drug effects Enzyme Inhibitors--pharmacology G1 Phase--drug effects Gene Expression Regulation, Enzymologic--drug effects Gene Expression Regulation, Leukemic--drug effects Humans Hydroxyurea--pharmacology Imatinib Mesylate Interleukin-1--pharmacology Intracellular Signaling Peptides and Proteins--metabolism K562 Cells Leukemia, Myelogenous, Chronic, BCR-ABL Positive--drug therapy Membrane Proteins--antagonists & inhibitors Piperazines--pharmacology Pyrazoles--pharmacology Pyrimidines--pharmacology S Phase--drug effects Sulfonamides--pharmacology