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Serum B-cell maturation antigen is elevated in multiple myeloma and correlates with disease status and survival.

British journal of haematology (2012-07-19)
Eric Sanchez, Mingjie Li, Alex Kitto, Jennifer Li, Cathy S Wang, Dylan T Kirk, Ori Yellin, Cydney M Nichols, Marissa P Dreyer, Cameryn P Ahles, Austin Robinson, Erik Madden, Gabriel N Waterman, Regina A Swift, Benjamin Bonavida, Ralph Boccia, Robert A Vescio, John Crowley, Haiming Chen, James R Berenson
RESUMEN

Although TNFRSF17 (also designated as B-cell maturation antigen (BCMA)) is expressed on tumour cells in B-cell malignancies, it has not been found in serum. The present study found that BCMA concentrations were higher in the supernatants of cultured bone marrow mononuclear cells from multiple myeloma (MM) patients than in healthy subjects. Serum BCMA levels were measured in samples from MM patients (n = 209), monoclonal gammopathy of undetermined significance (MGUS) individuals (n = 23) and age-matched controls (n = 40). BCMA was detected in the serum of untreated MM patients (n = 50) and levels were higher than in MGUS patients (P = 0·0157) and healthy subjects (P < 0·0001). Serum BCMA levels were higher among patients with progressive disease (n = 80) compared to those with responsive disease (n = 79; P = 0·0038). Among all MM patients, overall survival was shorter among patients whose serum BCMA levels were above the median (P = 0·001). We also demonstrated that sera from mice with human MM xenografts contained human BCMA, and levels correlated with the change in tumour volume in response to melphalan or cyclophosphamide with bortezomib. These results suggest that serum BCMA levels may be a new biomarker for monitoring disease status and overall survival of MM patients.

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Sigma-Aldrich
Monoclonal Anti-TNFRSF17 antibody produced in mouse, clone 1F10, purified immunoglobulin, buffered aqueous solution