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BCL6

3q27

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BCL6 partners in B-cell lymphoma
LAZ3, ZNF51

The BCL6 gene is a proto-oncogene, that encodes for a zinc-finger transcriptional repressor acting on a series of target genes implicated in T and B cell maturation(39), cell cycle control, apoptosis or inflammation. Its down regulation is necessary for the post-germinal center B cell maturation, whereas its expression is crucial for the germinal center formation.

BCL6 is a zinc-finger transcription repressor normally expressed exclusively within GC B cells, suggesting a critical role in the GC reaction. Indeed, BCL6 null animals fail to generate GCs in response to antigen. The down-regulation of BCL6 may be necessary for normal GC B cells to further differentiate into memory B cells or plasma cells.

Pathology

- Chromosomal translocations involving the BCL6 gene on band 3q27 are the most common genetic abnormalities in DLBCL, occurring in 35% to 40% of cases. Although several chromosomes may partner with 3q27, the most common translocations involve the immunoglobulin heavy-chain promoter (IGH promoter), resulting in constitutive expression of this normally developmentally regulated gene.

- In diffuse large b-cell lymphoma (DLBCL), dysregulated constitutive expression of BCL6 may lead to maturation arrest and confer a proliferative advantage.

- Recent studies identify a mechanism whereby BCL6 may regulate GC formation and lymphomagenesis via down-regulation of p53.

- Investigators postulate that BCL6 functions normally to suppress p53-mediated apoptosis of GC B cells in response to DNA damage during the GC reaction.

- Constitutive expression of BCL6 might decrease the p53-mediated apoptotic response to DNA damage, promoting persistence of malignant clones. A recently developed BCL6 transgenic mouse provides further insight into the precise role of this gene in lymphomagenesis.

- BCL6 rearrangements occur primarily in de novo DLBCL.

- No uniform effect on prognosis has been observed, likely due to multiple other contributing factors, including differential biology of the partner chromosome, concomitant genetic defects, SHM, and unidentified molecular substructure.

Summary

- BCL6 rearrangements in B-cell lymphomas

- translocation with Ig genes

- fusion genes

  • TFRC at 3q29 (MIM.190010)
  • RHOH at 4p13 by t(3;4)(q27;p13) BCL6-RHOH (MIM.602037)
  • SFRS3 at 6p21 by t(3;6)(q27;p21) BCL6-SFRS3 (SRP20) (MIM.603364)
  • PIM1 at 6p21 by t(3;6)(q27;p21) BCL6-PIM1
  • HIST1H4I at 6p22 by t(3;6)(q27;p22) BCL6-HIST1H4I (H4FM) (MIM.602833)
  • ZNFN1A1 at 7p12 by t(3;7)(q27;p12) BCL6-ZNFN1A1 (MIM.603023)
  • MYC (?) at 8q24 by t(3;8)(q27;q24)
  • 9p13 at t(3;9)(q27;p13)
  • POU2AF1 at 11q23 by t(3;11)(q27;q23)
  • GAPDH at 12p13
  • LCP1 at 13q14 by t(3;13)(q27;q14) BCL6-LCP1 (MIM.153430)
  • HSPCA at 14q32
  • 15q22 by t(3;15)(q27;q22)
  • IL21R at 16p11 by t(3;16)(q27;p11) BCL6-IL21R (MIM.109565)
  • MHC2TA at 16p13
  • 17q11 by t(3;17)(q27;q11)
  • EIF4A2 at 18p11

- BCL6 rearrangements in nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) (48%) (15339680)

- BCL6 rearrangements in follicular lymphoma grade 3B (FL3B)(centroblasts) (55%)

- BCL6 mutations in

  • pulmonary lymphoproliferative disorders(15153535)
    • mucosa-associated lymphoid tissue (MALT) lymphoma (40%) (15153535)
    • HIV-related (100%) (15153535)
    • EBV-related (40%) (15153535)
    • virus-negative lymphocytic interstitial pneumonia (LIP) (30%) (15153535)

P.S.


- AGCOH
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