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Brian Van Ness, PH.D.

Professor/ Department Head


Mailing Address:
University of Minnesota
Department of Genetics, Cell Biology, and Development
Box 806 Mayo
Cancer Center Research Bldg
Minneapolis, MN 55455
USA



Education:
Ph.D., University of Minnesota, 1979

Honors:
Scientific Advisory Board: International Myeloma Foundation
Scientific Advisory Board: Multiple Myeloma Research Foundation
Office:
14-287 Moos
P:612-624-9944
F:612-626-4915

Email:
vanne001@umn.edu

Lab:
14-115 Moos
P:612-624-9663

Areas of Research Strength:

Gene expression
Cancer genetics
Immunology
Genetic diagnostics
Mouse transgenics

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Research Techniques:

Gene profiling (expression arrays, SNPs)
Transfections
Flow cytometry
Transgenic mice
PCR

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Research Interests:

The research in the Van Ness lab is directed at defining genetic deregulation
that contributes to lymphoid malignancies, particularly multiple myeloma.
Multiple myeloma results from plasma cell expansion in the bone marrow,
and unfortunately is very hard to treat. This difficulty comes in part from
the variability in genetic and signaling pathways that are deregulated in the
plasma cells as well as the cells in the bone marrow microenvironment.
The lab is developing both cell lines and mouse models to explore how
different genes can influence disease progression and therapeutic response.
The lab is identifying some of the complexity of gene expression through
microarray expression profiling; and we have undertaken a collaborative project
to target gene deregulation that will contribute to models of plasma cell malignancy
in the mouse. The Van Ness lab is also working with both national and international
clinical groups to correlate genetic defects with disease outcome and response to
different therapies. The ultimate goal is to contribute to genetic characterization
of patients that will direct individualized therapy.

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Selected Publications:

Kyle, RA, Leong, T, Li, S, Oken MM, Kay, NE, Van Ness, B, and Greipp, PR. (2006) Complete Response in Multiple Myeloma: An Eastern Cooperative Oncology Group Study. Cancer (in press).

Cheung, WC, Kim, JS, Linden, M, Peng, L, Van Ness, B, Polakiewicz, RD, and Janz, S. (2005) The perils of abrogating myc-dependent apoptosis. CCR Frontiers in Science. 4:4-5.

Linden, M, Kirchoff, N, Kvitrud, M, and Van Ness, B. (2004) Abl-myc retroviral infection elicits bone marrow plasma cell tumors in Bcl-xL transgenic mice. Leukemia Research. 4:435-444.

Croonquist, P and Van Ness, B. (2005) The polycomb group protein Enhancer of Zeste Homologue 2 (EZH2) is an oncogene required for myeloma cell growth and the ras proliferative phenotype. Oncogene. 24:6269-6280.

Linden, M, Kirchhof, N, Carlson, C, and Van Ness, B. (2004) Targeted overexpression of BCL-xL in B lymphoid cells results in lymphoproliferative disease and plasma cell malignancies. Blood. 103:2779-2790.

Cheung, WC, Kim, JS, Linden, M, Van Ness, B. Polakiewicz, R, and Janz, S. Novel targeted deregulation of c-myc and bcl-xL combine to cause plasma cell malignancies in mice. (2004) J. Clinical Invest. 113: 1763-1773.

Linden M, Kirchhof N, Carlson C and Van Ness B (2004) Targeted overexpression of BCL-xL in B lymphoid cells results in lymphoproliferative disease and plasma cell malignancies. Blood. 103: 2779-2790.

Croonquist P, Linden M, Zhao F, and Van Ness B (2003) Gene Profiling of a Myeloma Cell Liine Reveals Similarities and Unique Signatures among IL-6 response, N-ras Activating Mutations and co-culture with bone Marrow Stromal Cells. Blood 2581-2592.

Kyle, RA, et al...Van Ness, BG(The International Myeloma Working Group). (2003) Criteria for the classification of monoclonal gammopathies, multiple myeloma and related disorders: a report of the International Myeloma Working Group. B J Hematol. 121:749-757.

Durie BG, Kyle RA, Belch A, Bensinger W, Blade J, Boccadoro M, Child JA, Comenzo R, Djulbegovic B, Fantl D, Gahrton G, Harousseau JL, Hungria V, Joshua D, Ludwig H, Mehta J, Morales AR, Morgan G, Nouel A, Oken M, Powles R, Roodman D, San Miguel J, Shimizu K, Singhal S, Sirohi B, Sonneveld P, Tricot G, Van Ness B. Myeloma management guidelines: a consensus report from the Scientific Advisors of the International Myeloma Foundation. Hematol J. 2003; 4(6): 379-98.

Fonseca, R., Blood, E., Rue, M., Harrington, D., Oken, M., Kyle, R., Dewald, G., Van Ness, B., Van Weir, S., Henderson, K., Bailey, R., and Greipp, P. (2003) Clinical and biological implications of recurrent genomic aberrations in myeloma. Blood. 101:4569-4575.

Croonquist, P. Linden, M, Zhao, F, and Van Ness, B. (2003) Gene Profiling of a Myeloma Cell Line Reveals Similarities and Unique Signatures among IL-6 response, N-ras Activating Mutations and co-culture with Bone Marrow Stromal Cells. Blood. 2581-2592

Hu, L., Shi, Y., Hsu, J., Gera, J., Van Ness, B., and Lichtenstein, A. (2003) Downstream effectors of oncogenic ras in multiple myeloma cells. Blood. 101(8):3126-3135

Cheung,, W. and Van Ness, B. (2002) Distinct IL-6 signal transduction leads to growth arrest and death in B cells or growth promotion and cell survival in myeloma cells. Leukemia. 16(6):1182-8

Rowley, M., and Van Ness, B. (2002) Activation of N-ras and K-ras induced by interleukin-6 in a myeloma cell line: implications for disease progression and therapeutic response. Oncogene 21:8679-8775.



To view these and other publications visit http://www.ncbi.nlm.nih.gov/PubMed
search menu should say PubMed
type Van Ness B in the avaliable line

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Related Links:

Bank On A Cure, with the International Myeloma Foundation

BOAC SNP info Table (Excel) File


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Bcl-xL transgenic mouse develops myeloma like bone disease

Sternum of transgenic Bcl-xL transgenic mouse infiltrated with malignant plasma cells