Gururajan Murali, Jennings C Darrell, Bondada Subbarao
Department of Microbiology, Immunology and Molecular Genetics, Sanders Brown Center on Aging, University of Kentucky, Lexington, KY 40536, USA.
J Immunol. 2006 May 15;176(10):5715-9. doi: 10.4049/jimmunol.176.10.5715.
B lymphomas account for the majority of the lymphoma cases. BCR expression appears to be important for B lymphoma because most oncogenes are translocated to nonrearranged Ig loci and because all of the variants that arise in anti-idiotypic Ab-treated lymphoma patients remain BCR positive. Based on this and the fact that BCR is required for mature B cell survival, we tested the requirement for continued expression of BCR for the growth and survival of B lymphoma cells. Using Igalpha or Igbeta-specific small interfering RNA (siRNA) to inhibit BCR expression, we demonstrate for the first time that constitutive signaling by BCR is critical for survival and proliferation of both murine and human B lymphoma cells. The BCR signals in lymphoma appear to be mediated by Syk, as it is constitutively active in a variety of B lymphoma cells. Blocking Syk activity by selective inhibitors suppresses growth of several murine and human B lymphomas.
B淋巴瘤占淋巴瘤病例的大多数。BCR表达似乎对B淋巴瘤很重要,因为大多数癌基因易位到未重排的Ig基因座,并且因为在抗独特型抗体治疗的淋巴瘤患者中出现的所有变体仍为BCR阳性。基于此以及成熟B细胞存活需要BCR这一事实,我们测试了BCR持续表达对B淋巴瘤细胞生长和存活的必要性。使用Igalpha或Igbeta特异性小干扰RNA(siRNA)抑制BCR表达,我们首次证明BCR的组成型信号传导对小鼠和人B淋巴瘤细胞的存活和增殖至关重要。淋巴瘤中的BCR信号似乎由Syk介导,因为它在多种B淋巴瘤细胞中组成型激活。用选择性抑制剂阻断Syk活性可抑制几种小鼠和人B淋巴瘤的生长。