PAX5 is one of the key transcription factors mediating differentiation of B-lymphocytes. It transcriptionally activates and represses a very large number of genes that permits the development of B-lymphocytes and prevents differentiation to T-lymphocytes or myeloid cells. We examined by SNP chip 633 acute lymphocytic leukemia (ALL) samples for PAX5 alterations (469 pediatric cases, 70 pediatric relapse cases, 74 adult cases and 50 ALL samples growing as xenografts). PAX5 genomic abnormalities occurred in H 27% of the samples including 26 PAX5 fusions to one of 5 other genes. Overall goal of the grant is to understand the clinical and pathologic significance of PAX5 alterations in ALL.
Specific Aim 1 will determine frequency of genomic abnormalities of PAX5 in ALL and determine their clinical impact.
Specific Aim 2 will define and understand the aberrant functions of PAX5 fusion and mutant proteins in ALL (Ex Vivo Studies). Studies will include gel retardation and reporter gene analysis as well as testing the ability of these proteins transcriptionally to activate selected target genes. Detailed studies will be done using two of the PAX5 fusions [PAX5-ETV6;PAX5- C20orf112 (C20)] including genome-wide identification of target genes of PAX5 fusion proteins in ALL using cDNA microarray analysis and high through-put ChIP sequencing studies. Comprehensive validation of the results will use a variety of techniques. Also, effect of PAX5 fusion proteins on hematopoietic cell differentiation will be determined.
Specific Aim 3 will use in vivo models to examine the aberrant function of PAX5 fusions and deletions. First, we will determine if expression of PAX5 fusion proteins disrupts normal steady-state lymphopoiesis or hematopoiesis by impairing differentiation, promoting survival and/or proliferation of specific compartments? Second, we will identify secondary events that synergize with PAX5 fusion proteins to induce ALL. Third, we will determine if PAX5 deletions affect the course of human Ph1+ ALL xenografts. In summary, we will for the first time, correlate PAX5 alterations with clinical and pathological characteristics of the patients and define fully the functional significance of these alterations. These studies will have importance for classification of the disease, offer new therapeutic targets and foster our understanding of the pathogenesis of ALL.

Public Health Relevance

PAX5 lymphoid transcription factor is structurally abnormal in approximately 27% of 634 ALL samples. Our studies will for the first time provide insights into the clinical significance of PAX5 alterations in acute lymphocyte leukemia (ALL), as well as provide an understanding of the functional ramifications of PAX5 alterations in ALL. Our studies should lead to new therapeutic targets for acute leukemias, as well as provide a greater understanding of the biology of ALL.

National Institute of Health (NIH)
National Cancer Institute (NCI)
Research Project (R01)
Project #
Application #
Study Section
Hematopoiesis Study Section (HP)
Program Officer
Mufson, R Allan
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Cedars-Sinai Medical Center
Los Angeles
United States
Zip Code
Sun, Qiao-Yang; Ding, Ling-Wen; Xiao, Jin-Fen et al. (2015) SETDB1 accelerates tumourigenesis by regulating the WNT signalling pathway. J Pathol 235:559-70
Ding, L-W; Sun, Q-Y; Lin, D-C et al. (2015) LNK (SH2B3): paradoxical effects in ovarian cancer. Oncogene 34:1463-74
Okamoto, Ryoko; Gery, Sigal; Gombart, Adrian F et al. (2014) Deficiency of CCAAT/enhancer binding protein-epsilon reduces atherosclerotic lesions in LDLR-/- mice. PLoS One 9:e85341
Lin, De-Chen; Hao, Jia-Jie; Nagata, Yasunobu et al. (2014) Genomic and molecular characterization of esophageal squamous cell carcinoma. Nat Genet 46:467-73
Lin, De-Chen; Meng, Xuan; Hazawa, Masaharu et al. (2014) The genomic landscape of nasopharyngeal carcinoma. Nat Genet 46:866-71
Lin, Lehang; Gaut, Daria; Hu, Kaishun et al. (2014) Dual targeting of glioblastoma multiforme with a proteasome inhibitor (Velcade) and a phosphatidylinositol 3-kinase inhibitor (ZSTK474). Int J Oncol 44:557-62
Okamoto, Ryoko; Gery, Sigal; Kuwayama, Yoshio et al. (2014) Novel Gemini vitamin D3 analogs: large structure/function analysis and ability to induce antimicrobial peptide. Int J Cancer 134:207-17
Zheng, Yun; Gery, Sigal; Sun, Haibo et al. (2014) KPT-330 inhibitor of XPO1-mediated nuclear export has anti-proliferative activity in hepatocellular carcinoma. Cancer Chemother Pharmacol 74:487-95
Zhou, Yan; Zhao, Conghui; Gery, Sigal et al. (2014) Off-target effects of c-MET inhibitors on thyroid cancer cells. Mol Cancer Ther 13:134-43
Chien, Wenwen; Ding, Ling-Wen; Sun, Qiao-Yang et al. (2014) Selective inhibition of unfolded protein response induces apoptosis in pancreatic cancer cells. Oncotarget 5:4881-94

Showing the most recent 10 out of 193 publications