Research Topics
Species | Jonathan J KeatsSummaryAffiliation: Mayo Clinic Country: USA Publications
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Detail Information
Publications
Ten years and counting: so what do we know about t(4;14)(p16;q32) multiple myelomaJonathan J Keats
Department of Oncology, University of Alberta and Cross Cancer Institute, Edmonton, Canada
Leuk Lymphoma 47:2289-300. 2006..Unfortunately, despite the known association with outcome, an understanding of the mechanism(s) whereby the translocation contributes to developing and maintaining this aggressive form of myeloma remains elusive...
Overexpression of transcripts originating from the MMSET locus characterizes all t(4;14)(p16;q32)-positive multiple myeloma patientsJonathan J Keats
Department of Oncology, University of Alberta and Cross Cancer Institute, 11560 University Ave, Edmonton, AB, T6G 1Z2, Canada
Blood 105:4060-9. 2005..In contrast, RE-IIBP is universally dysregulated and also potentially functional in all t(4;14)POS patients irrespective of fibroblast growth factor receptor 3 (FGFR3) expression or breakpoint type...
SSX cancer testis antigens are expressed in most multiple myeloma patients: co-expression of SSX1, 2, 4, and 5 correlates with adverse prognosis and high frequencies of SSX-positive PCsBrian J Taylor
Department of Oncology, Cross Cancer Institute, and Department of Medicine, University of Alberta, Edmonton, Alberta, Canada
J Immunother (1997) 28:564-75. 2005..These results demonstrate that SSX is a frequently expressed CTA in MM and highlight its potential as an MM vaccine candidate...
Receptor for hyaluronan-mediated motility correlates with centrosome abnormalities in multiple myeloma and maintains mitotic integrityChristopher A Maxwell
Department of Oncology, University of Alberta and Cross Cancer Institute, 11560 University Avenue, Edmonton, Alberta, Canada T6G 1Z2
Cancer Res 65:850-60. 2005..We postulate that augmentation of RHAMM expression within human cancers, including myeloma, can directly affect centrosomal structure and spindle integrity and potentially modulate apoptotic and cell cycle progression pathways...
The selective Aurora B kinase inhibitor AZD1152 is a potential new treatment for multiple myelomaRobert P Evans
Department of Oncology, University of Alberta Cross Cancer Institute, Edmonton, AB, Canada
Br J Haematol 140:295-302. 2008..AZD1152 shows promise in these preclinical studies as a novel treatment for MM...
In multiple myeloma, t(4;14)(p16;q32) is an adverse prognostic factor irrespective of FGFR3 expressionJonathan J Keats
Department of Oncology, University of Alberta and Cross Cancer Institute, Edmonton, Canada
Blood 101:1520-9. 2003..003). The presence of t(4;14) is also predictive of poor response to first-line chemotherapy (P =.05). These results indicate a significant clinical impact of the t(4;14) translocation in MM that is independent of FGFR3 expression...
RHAMM expression and isoform balance predict aggressive disease and poor survival in multiple myelomaChristopher A Maxwell
Department of Medical Oncology, Cross Cancer Institute, 11560 University Ave, Edmonton, AB, T6G 1Z2, Canada
Blood 104:1151-8. 2004..The RHAMM-exon4/RHAMMFL ratio in diagnostic bone marrow samples (n=101, Alberta) is an independent prognostic factor. Thus, expression and splicing of RHAMM are important molecular determinants of disease severity in MM...
Identification of a potent natural triterpenoid inhibitor of proteosome chymotrypsin-like activity and NF-kappaB with antimyeloma activity in vitro and in vivoRodger E Tiedemann
Division of Hematology and Oncology, Comprehensive Cancer Center, Mayo Clinic, Scottsdale, AZ 85259, USA
Blood 113:4027-37. 2009....
Leukemic B cells clonally identical to myeloma plasma cells are myelomagenic in NOD/SCID miceLinda M Pilarski
Department of Oncology, University of Alberta and Cross Cancer Institute, Edmonton, Alberta, Canada
Exp Hematol 30:221-8. 2002....
Promiscuous mutations activate the noncanonical NF-kappaB pathway in multiple myelomaJonathan J Keats
Comprehensive Cancer Center, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA
Cancer Cell 12:131-44. 2007..These results highlight the critical importance of the NF-kappaB pathway in the pathogenesis of multiple myeloma...
