Neoplastic plasma cell aberrant antigen expression patterns and their association with genetic abnormalities

• Published in: Leukemia & lymphoma Vol. 56; no. 2; pp. 426 - 433
• Main Authors: Salama, Mohamed E., Du, Shouying, Efimova, Olga, Heikal, Nahla M., Wendlandt, Erik, Toydemir, Reha M., South, Sarah, Perkins, Sherrie L., Hussong, Jerry W., Zhan, Fenghuang
• Format: Journal Article
• Language: English
• Published: United States Informa Healthcare 01.02.2015
• Subjects: Antigens, CD - genetics; Antigens, CD - metabolism; Antigens, CD20 - genetics; Antigens, CD20 - metabolism; Antigens, Neoplasm - genetics; Antigens, Neoplasm - metabolism; Bone Marrow - metabolism; Bone Marrow - pathology; CD52 Antigen; CD56 Antigen - genetics; CD56 Antigen - metabolism; Chromosome Aberrations; Flow Cytometry; Gene Expression Profiling; Glycoproteins - genetics; Glycoproteins - metabolism; Humans; In Situ Hybridization, Fluorescence; Multiple Myeloma - genetics; Multiple Myeloma - metabolism; Multiple Myeloma - pathology; Plasma Cells - metabolism; Plasma Cells - pathology; Proto-Oncogene Proteins c-kit - genetics; Proto-Oncogene Proteins c-kit - metabolism; molecular genetics; Cytogenetics; myeloma
• ISSN: 1042-8194; 1029-2403
• DOI: 10.3109/10428194.2014.931951

Abstract Little is known about aberrant antigen expression patterns and their association with cytogenetic aberrations in multiple myeloma (MM). We examined the correlation between flow cytometry and florescence in situ hybridization (FISH) in 167 marrow specimens with MM. Gene expression profiling of CD56, CD117, CD52 and CD20 mRNA in plasma cells (PCs) from patients treated on Total Therapy 2 and Total Therapy 3 trials were also evaluated. Higher expression of CD56 and CD117 was associated with hyperdiploidy. High CD52 mRNA expression was associated with c-MAF and FGFR3 subgroups. Higher expression of CD56 mRNA, but lower Kit expression, were noted in association with FGFR3. In contrast, the c-MAF subgroup showed high Kit expression but lacked NCAM mRNA expression. CKS1B amplification showed positive correlation with CD52 (p = 0.0065) but negative correlation with CD20 (p = 0.0207). These findings indicate that phenotypic differences in MM are associated with distinct genetic subgroups, which potentially has important diagnostic and prognostic value.