The overall objective in this A2 grant is to determine the potential use of microRNAs (miRNAs) miR-15a/16 as therapy for chronic lymphocytic leukemia (CLL). This will be studied in vitro and in vivo in the murine model, NZB and in ex vivo CLL patient samples. We have described the NZB strain as a valid model of CLL that faithfully replicates the human disease. As they age, NZB develop a malignant expansion of B -1 cells with dull CD5 expression, CD11b, and B220. These mice also characteristically make an IgM anti- erythrocyte autoantibody response and polyclonal autoantibodies. We have found linkage of NZB lymphoproliferative disease with a region of mouse chromosome 14, in which there is a germline mutation in the mir-15a/16-1 loci in the 3'region flanking mir-16-1 and decreased expression of the mature miR-15a and miR-16 in NZB lymphoid sources relative to normal strain sources. A similar mutation has been found in the rare CLL patient, with the majority of CLL patients expressing deletions in this loci in the malignant clone resulting in decreased expression of miR-15a and miR-16. In the presence of decreased miR-15a/16, mRNA targets of these microRNAs are elevated including anti-apoptosis genes (bcl family) and cell cycle regulators (cyclin D1), which have been found to be increased in NZB malignant cells and critical to survival pathways for the malignant cells. An inability to respond to growth regulation and apoptosis induction may result in treatment resistant disease, much of which may be mediated by a defect in this important miRNA. The hypothesis to be tested is that abnormalities in miRNAs miR-15a and miR-16 are an underlying defect giving rise to CLL. In this A2 grant, (Specific Aim #1) normal mice will be engineered to have the NZB mir- 15a/16-1 loci to determine if the mutation results in decreased mature miR-15a and miR-16 levels, as well as effects on B-1 cell expansions. Next (Specific Aim #2), the potential therapeutic effect of in vivo lentiviral delivery of exogenous miR-15a/16 in the NZB model of CLL will be determined. The mechanism of action of miR-16 will be determined in both NZB malignant B cells (Specific Aim #3) and CLL patient samples (Specific Aim #4). The overall outcome of these studies will be to determine the potential efficacy of miR- 15a/16 delivery as a therapy or an adjuvant to chemotherapy in CLL.

Public Health Relevance

CLL is the most common leukemia in the Western world and, as the average age in the US rises, the number of affected individuals will also increase. Studies in CLL patient samples have demonstrated decreased levels of the microRNAs, miR-15a/16, which is also found in the NZB mouse model. Therapies directed at miRNAs developed in the NZB mouse model can be translated into the human situation due to the highly conserved nature of miRNAs.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA129826-03
Application #
8197568
Study Section
Basic Mechanisms of Cancer Therapeutics Study Section (BMCT)
Program Officer
Arya, Suresh
Project Start
2009-12-07
Project End
2012-11-30
Budget Start
2011-12-01
Budget End
2012-11-30
Support Year
3
Fiscal Year
2012
Total Cost
$313,989
Indirect Cost
$112,714
Name
University of Medicine & Dentistry of NJ
Department
Pathology
Type
Schools of Medicine
DUNS #
623946217
City
Newark
State
NJ
Country
United States
Zip Code
07107
Kasar, S; Salerno, E; Yuan, Y et al. (2012) Systemic in vivo lentiviral delivery of miR-15a/16 reduces malignancy in the NZB de novo mouse model of chronic lymphocytic leukemia. Genes Immun 13:109-19
Shim, Youn K; Middleton, Dannie C; Caporaso, Neil E et al. (2010) Prevalence of monoclonal B-cell lymphocytosis: a systematic review. Cytometry B Clin Cytom 78 Suppl 1:S10-8
Salerno, Erica; Yuan, Yao; Scaglione, Brian J et al. (2010) The New Zealand black mouse as a model for the development and progression of chronic lymphocytic leukemia. Cytometry B Clin Cytom 78 Suppl 1:S98-109
Scaglione, Brian J; Salerno, Erica; Balan, Murugabaskar et al. (2007) Murine models of chronic lymphocytic leukaemia: role of microRNA-16 in the New Zealand Black mouse model. Br J Haematol 139:645-57