TY - JOUR
T1 - Therapeutic targeting of the BCL6 oncogene for diffuse large B-cell lymphomas
AU - Parekh, Samir
AU - Prive, Gilbert
AU - Melnick, Ari
N1 - Funding Information:
GGP is supported by the National Cancer Institute of Canada/Canadian Cancer Society and the Canadian Institutes of Health Research. AMM is supported by NCI R01 CA104348, the G&P foundation, Chemotherapy foundation, and the Leukemia and lymphoma Society of America. Both GGP and AMM are supported by a program grant from the Samuel Waxman Cancer Research Foundation.
PY - 2008/5
Y1 - 2008/5
N2 - BCL6 is a transcriptional repressor often expressed constitutively in diffuse large B-cell lymphomas (DLBCL) due to mutations of its genomic locus. BCL6 mediates aberrant survival, proliferation, genomic instability and differentiation blockade in DLBCL cells. The biochemical study of BCL6 mediated gene repression has provided the basis for design of agents that inhibit BCL6 and kill lymphoma cells. The repressor activity of the BCL6 BTB domain is particularly well defined from the structural standpoint. Design of inhibitors targeting BCL6 BTB domain protein interaction surfaces appears to be an effective approach, which reactivates important BCL6 target genes and readily kills DLBCL cells. Targeting other domains of BCL6 or using histone deacetylase inhibitors to overcome BCL6 mediated repression may also be useful. Recent studies in DLBCL transcriptional signatures have revealed a subset of DLBCLs that are particularly dependent on BCL6 to maintain their survival and these patients could be candidates for clinical trials of BCL6 inhibitors.
AB - BCL6 is a transcriptional repressor often expressed constitutively in diffuse large B-cell lymphomas (DLBCL) due to mutations of its genomic locus. BCL6 mediates aberrant survival, proliferation, genomic instability and differentiation blockade in DLBCL cells. The biochemical study of BCL6 mediated gene repression has provided the basis for design of agents that inhibit BCL6 and kill lymphoma cells. The repressor activity of the BCL6 BTB domain is particularly well defined from the structural standpoint. Design of inhibitors targeting BCL6 BTB domain protein interaction surfaces appears to be an effective approach, which reactivates important BCL6 target genes and readily kills DLBCL cells. Targeting other domains of BCL6 or using histone deacetylase inhibitors to overcome BCL6 mediated repression may also be useful. Recent studies in DLBCL transcriptional signatures have revealed a subset of DLBCLs that are particularly dependent on BCL6 to maintain their survival and these patients could be candidates for clinical trials of BCL6 inhibitors.
KW - Lymphoma and Hodgkin disease
KW - Pharmacotherapeutics
KW - Transcription factor changes
UR - http://www.scopus.com/inward/record.url?scp=46749154664&partnerID=8YFLogxK
U2 - 10.1080/10428190801895345
DO - 10.1080/10428190801895345
M3 - Review article
C2 - 18452090
AN - SCOPUS:46749154664
SN - 1042-8194
VL - 49
SP - 874
EP - 882
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 5
ER -