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Prepublished online as a Blood First Edition Paper on September 25, 2003; DOI 10.1182/blood-2003-06-2043. This Article Full Text (PDF) All Versions of this Article: 2003-06-2043v1 103/2/689    most recent Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Rights and Permissions Citing Articles Citing Articles via HighWire Citing Articles via CrossRef Citing Articles via Google Scholar Google Scholar Articles by Novak, A. J Articles by Jelinek, D. F Search for Related Content PubMed PubMed Citation Articles by Novak, A. J Articles by Jelinek, D. F Social Bookmarking                   What's this? Submitted June 27, 2003 Accepted September 15, 2003 Expression of BCMA, TACI, and BAFF-R in multiple myeloma: a mechanism for growth and survival Anne J Novak, Jaime R Darce, Bonnie K Arendt, Brandon Harder, Kathy Henderson, Wayne Kindsvogel, Jane A Gross, Philip R Greipp, and Diane F Jelinek* Department of Immunology, Mayo Foundation, Rochester, MN, USA Department of Internal Medicine, Mayo Foundation, Rochester, MN, USA Zymogenetics, Seattle, WA, USA * Corresponding author; email: jelinek.diane{at}mayo.edu. Multiple myeloma (MM) is a progressive disease that is thought to result from multiple genetic insults to the precursor plasma cell that ultimately affords the tumor cell with proliferative potential despite its differentiated phenotype and resistance to undergoing apoptosis. Altered expression of anti-apoptotic factors as well as growth factors have been described in a significant number of patients. However, the key regulatory elements that control myeloma development and progression remain largely undefined. Because of the knowledge that BLyS, a tumor necrosis factor (TNF) family member shown to be critical for maintenance of normal B cell development and homeostasis, promotes the survival of malignant B cells, we began a coordinated study of BLyS and its receptors in MM. All MM cells studied expressed one or more of three known receptors (BCMA, TACI, and BAFF-R) for BLyS; however, the pattern of expression was variable. Additionally, we provide evidence that BLyS can modulate the proliferative capacity and survival of MM cells. Finally, we provide evidence that BLyS is expressed by MM cells and is present in the bone marrow of MM patients. Expression of BCMA, TACI, and BAFF-R by MM taken together with the ability of BLyS to support MM cell growth and survival has exciting implications as they may be potential therapeutic targets. 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