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Blood ; 105(12): 4784-91, 2005 Jun 15.
Article in English | MEDLINE | ID: mdl-15731178

ABSTRACT

Cyclooxygenase 2 (COX-2) is an inflammation-associated enzyme involved in the pathogenesis of many solid tumors, but little is known about its presence and role in hematologic neoplasms. Multiple myeloma (MM) is known to involve a deregulated cytokine network with secretion of inflammatory mediators. We thus decided to investigate the involvement of COX-2 in this neoplasm. Western blotting (WB) was used to evaluate 142 bone marrow (BM) specimens, including MM and monoclonal gammopathy of undetermined significance (MGUS). Selected cases under-went further evaluation by WB on purified CD138(+) cells, immunohistochemistry (IC), and real-time polymerase chain reaction (PCR) for mRNA expression. COX-2 was expressed in 11% (2 of 18) of MGUS specimens, 31% (29 of 94) of MM at diagnosis, and 47% (14 of 30) of MM with relapsed/refractory disease. COX-2 positivity was associated with a poor outcome in terms of progression-free (18 vs 36 months; P < .001) and overall survival (28 vs 52 months; P < .05). Real-time PCR showed COX-2 mRNA overexpression. IC and cell separation studies demonstrated COX-2 expression to be restricted to malignant plasma cells. This is the first report of the presence and prognostic role of COX-2 expression in MM. Future studies will assess COX-2 involvement in other hematologic tumors and its potential use as a therapeutic or chemo-preventive target in onco-hematology.


Subject(s)
Multiple Myeloma/diagnosis , Multiple Myeloma/enzymology , Prostaglandin-Endoperoxide Synthases/biosynthesis , Adult , Aged , Blotting, Western , Bone Marrow Cells/cytology , Bone Marrow Cells/metabolism , Cell Line, Tumor , Cyclooxygenase 2 , DNA, Complementary/metabolism , Disease-Free Survival , Drug Resistance, Neoplasm , Female , Humans , Immunohistochemistry , Inflammation , Male , Membrane Glycoproteins/biosynthesis , Membrane Proteins , Middle Aged , Prognosis , Proteoglycans/biosynthesis , RNA, Messenger/metabolism , Recurrence , Reverse Transcriptase Polymerase Chain Reaction , Syndecan-1 , Syndecans , Time Factors , Treatment Outcome
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