Common mechanisms for the regulation of B cell differentiation and transformation by the transcriptional repressor protein BCL-6

被引:14
|
作者
Kusam, Saritha
Dent, Alexander
机构
[1] Indiana Univ, Sch Med, Walther Oncol Ctr, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[2] Walther Canc Inst, Indianapolis, IN 46208 USA
关键词
BCL-6; bcl6; B cell; differentiation; germinal center; plasma cell; immortalization; telomerase; non-Hodgkin's lymphoma;
D O I
10.1007/BF02697368
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The BCL-6 transcriptional repressor protein is a critical regulator of normal B cell differentiation and BCL-6 has recently been shown to act as an oncogene in several mouse model systems. The molecular pathways by which BCL-6 regulates B cell differentiation and also promotes the transformation of primary B cells are undoubtedly related; however, these pathways are poorly understood The commonly accepted model for BCL-6 function in B cells is that BCL-6 inhibits the terminal differentiation of activated B cells into plasma cells and that deregulation of BCL-6 expression leads to an inhibition of terminal differentiation and continued proliferation. BCL-6 induces a germinal-center phenotype in primary B cells by unknown mechanisms, and can reverse the terminal differentiation of plasma cell tumor lines. BCL-6 can promote the immortalization of primary B cells and can augment telomerase activity. The role of the vast majority of BCL-6 target genes and interacting proteins in normal B cell differentiation and B cell transformation is essentially unresolved and is an important area for future investigation.
引用
收藏
页码:177 / 186
页数:10
相关论文
共 50 条
  • [41] BCL-6 represses genes that function in lymphocyte differentiation, inflammation, and cell cycle control
    Shaffer, AL
    Yu, X
    He, YS
    Boldrick, J
    Chan, EP
    Staudt, LM
    IMMUNITY, 2000, 13 (02) : 199 - 212
  • [42] Post-transcriptional regulation of constitutive and IFN-gamma inducible BCL-6 gene expression
    Zhou, G
    Chau, KY
    Tai, AKF
    DallaFavera, R
    Ono, SJ
    JOURNAL OF LEUKOCYTE BIOLOGY, 1997, : 115 - 115
  • [43] B-cell development - BCL-6 recruits new team member
    Minton, K
    NATURE REVIEWS IMMUNOLOGY, 2004, 4 (11) : 839 - 839
  • [44] The proto-oncogene BCL-6 in normal and malignant B cell development
    Niu, HF
    HEMATOLOGICAL ONCOLOGY, 2002, 20 (04) : 155 - 166
  • [45] BCL-6 Gene Abnormalities are Common in Primary Central Nervous System Diffuse Large B-Cell Lymphoma
    Martin, Sarah
    Czader, Magdalena
    Al-Abbadi, Mousa
    Stohler, Ryan
    Vance, Gail
    Hattab, Eyas
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2010, 69 (05): : 548 - 549
  • [46] A purine scaffold Hsp90 inhibitor destabilizes BCL-6 and has specific antitumor activity in BCL-6–dependent B cell lymphomas
    Leandro C Cerchietti
    Eloisi C Lopes
    Shao Ning Yang
    Katerina Hatzi
    Karen L Bunting
    Lucas A Tsikitas
    Alka Mallik
    Ana I Robles
    Jennifer Walling
    Lyuba Varticovski
    Rita Shaknovich
    Kapil N Bhalla
    Gabriela Chiosis
    Ari Melnick
    Nature Medicine, 2009, 15 : 1369 - 1376
  • [47] Novel BCL-6 binding proteins identified by LC-MS/MS suggest a broader role for BCL-6 in B-cell function
    Miles, RR
    Crockett, DK
    Lim, MS
    Elenitoba-Johnson, KSJ
    LABORATORY INVESTIGATION, 2005, 85 : 242A - 242A
  • [48] Expression of the bcl-6 protein correlates with overall survival in patients with primary cutaneous large B cell lymphoma
    Sundram, U
    Mraz-Gerhard, S
    Storz, M
    Natkunam, Y
    Hoppe, R
    Kim, Y
    Kohler, S
    MODERN PATHOLOGY, 2003, 16 (01) : 100A - 100A
  • [49] BCL-6 gene mutations in primary cutaneous B-cell lymphomas
    Gianelli, U
    Cerri, A
    Cassani, B
    Moneghini, L
    Raviele, PR
    Berti, E
    Bosari, S
    HAEMATOLOGICA, 2004, 89 (05) : 624 - 626
  • [50] BCL-6 protein expression predicts improved survival in patients with diffuse large B-cell lymphoma
    Natkunam, Y
    Warnke, R
    Alizadeh, A
    Tibshirani, R
    Horning, S
    van de Rijn, M
    LABORATORY INVESTIGATION, 2001, 81 (01) : 173A - 173A