Research Topics
Species | Denise K WaltersSummaryAffiliation: Oregon Health and Science University Country: USA Publications
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Detail Information
Publications
Phosphoproteomic analysis of AML cell lines identifies leukemic oncogenesDenise K Walters
Department of Hematology and Oncology, Howard Hughes Medical Institute, Oregon Health and Science University Cancer Institute, 3181 Sam Jackson Park Road, and Portland VA Medical Center, Portland, OR 97239, USA
Leuk Res 30:1097-104. 2006..This study illustrates the benefit of LC-MS/MS mass spectrometry and siRNA for the identification of novel targets and mutations...
RNAi-induced down-regulation of FLT3 expression in AML cell lines increases sensitivity to MLN518Denise K Walters
Department of Hematology and Oncology, Howard Hughes Medical Institute, Oregon Health and Science University, and Portland Veterans Affairs VA Medical Center, 3181 Sam Jackson Park Rd, Portland, OR 97239, USA
Blood 105:2952-4. 2005..Furthermore, siRNA-induced down-regulation of FLT3 increased the sensitivity of both cell lines to treatment with the FLT3 inhibitor MLN518. This illustrates the potential benefit of combined therapeutic approaches...
Activating alleles of JAK3 in acute megakaryoblastic leukemiaDenise K Walters
Howard Hughes Medical Institute, Portland, Oregon 97239, USA
Cancer Cell 10:65-75. 2006..These findings illustrate the biological importance of gain-of-function JAK3 mutations in leukemogenesis and demonstrate the utility of proteomic approaches to identifying clinically relevant mutations...
Combined Abl inhibitor therapy for minimizing drug resistance in chronic myeloid leukemia: Src/Abl inhibitors are compatible with imatinibThomas O'Hare
Howard Hughes Medical Institute, Oregon Health and Science University, Portland 97239, USA
Clin Cancer Res 11:6987-93. 2005..As combination therapy is frequently used to prevent emergence of resistance, the combination of imatinib with an inhibitor of imatinib-resistant Bcr-Abl mutants (e.g., Src/Abl inhibitors AP23848 and BMS-354825) was investigated...
RNAi screening of the tyrosine kinome identifies therapeutic targets in acute myeloid leukemiaJeffrey W Tyner
Division of Hematology and Medical Oncology, Oregon Health and Science University Cancer Institute, Portland, USA
Blood 111:2238-45. 2008..This technique, with additional development, might eventually offer the potential to match specific therapies with individual patients based on a functional assay...
In vitro activity of Bcr-Abl inhibitors AMN107 and BMS-354825 against clinically relevant imatinib-resistant Abl kinase domain mutantsThomas O'Hare
Howard Hughes Medical Institute, Oregon Health and Science University Cancer Institute, Portland 97239, USA
Cancer Res 65:4500-5. 2005..Thus, both inhibitors hold promise for treating imatinib-refractory CML...
AMN107: tightening the grip of imatinibDenise K Walters
Howard Hughes Medical Institute, Oregon Health and Science University Cancer Institute, Portland, Oregon, 97239, USA
Cancer Cell 7:117-9. 2005..The implications of these results, and the potential role this and other novel ABL inhibitors may have in treating patients with CML, are discussed...
Phosphotyrosine profiling identifies the KG-1 cell line as a model for the study of FGFR1 fusions in acute myeloid leukemiaTing Lei Gu
Cell Signaling Technology, Inc, 3 Trask Lane, Danvers, MA 01923, USA
Blood 108:4202-4. 2006..Thus, the KG-1 cell line provides an in vitro model for the study of FGFR1 fusions associated with leukemia and for the analysis of small molecule inhibitors against FGFR1 fusions...
Transactivation of gp130 in myeloma cellsJena D French
Department of Immunology, Mayo Graduate and Medical Schools, Mayo Clinic, Rochester, MN 55905, USA
J Immunol 170:3717-23. 2003..Finally, transactivation of gp130 may be a common theme in myeloma cells, perhaps providing a mechanism for enhanced or qualitatively distinct cellular responses to specific stimuli...
Atypical expression of ErbB3 in myeloma cells: cross-talk between ErbB3 and the interferon-alpha signaling complexDenise K Walters
Department of Immunology, Tumor Biology Program, Mayo Graduate and Medical Schools, Mayo Clinic Foundation, Rochester, MN 55905, USA
Oncogene 22:3598-607. 2003..These results suggest that ErbB3 expression alone does not uniquely confer IFN-alpha growth responsiveness, but instead may amplify proliferation rates in MM cells that have acquired atypical expression of this receptor...
A role for Janus kinases in crosstalk between ErbB3 and the interferon-alpha signaling complex in myeloma cellsDenise K Walters
Department of Immunology, Tumor Biology Program, Mayo Graduate and Medical Schools, Mayo Clinic Foundation, Rochester, MN 55905, USA
Oncogene 23:1197-205. 2004..These findings validate our previous report of ErbB3 involvement in IFN-alpha-induced proliferation and further suggest that both Janus kinase members, Tyk2 and Jak1, play a role in the transactivation of ErbB3 in this model system...
A novel fusion of RBM6 to CSF1R in acute megakaryoblastic leukemiaTing Lei Gu
Cell Signaling Technology, Danvers, MA 01923, USA
Blood 110:323-33. 2007..These findings identify a novel potential therapeutic target in leukemogenesis, and demonstrate the utility of phosphoproteomic strategies for discovery of tyrosine kinase alleles...
Taurolidine: a novel anti-neoplastic agent induces apoptosis of osteosarcoma cell linesDenise K Walters
Laboratory for Orthopaedic Research, Department of Orthopaedics, Balgrist University Hospital, University of Zurich, Forchstrasse 340, 8008 Zurich, Switzerland
Invest New Drugs 25:305-12. 2007..These data indicate that taurolidine possesses potent anti-neoplastic activity against osteosarcoma cell lines and may have potential as a novel OS chemotherapeutic agent...
Cytotoxic effects of curcumin on osteosarcoma cell linesDenise K Walters
Laboratory for Orthopaedic Research, Department of Orthopaedics, Balgrist University Hospital, University of Zurich, Forchstrasse 340, 8008 Zurich, Switzerland
Invest New Drugs 26:289-97. 2008..These data indicate that the potent cytotoxic activity of curcumin on OS cell lines is mediated by induction of apoptotic processes. Thus, curcumin has potential to be a novel OS chemotherapeutic agent...
