Research Topics
Species | Michael S BobolaSummaryAffiliation: University of Washington Country: USA Publications
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Detail Information
Publications
O6-methylguanine-DNA methyltransferase, O6-benzylguanine, and resistance to clinical alkylators in pediatric primary brain tumor cell linesMichael S Bobola
Division of Neurosurgery, Department of Surgery and Hematology Oncology, Children s Hospital and Regional Medical Center, Seattle, Washington 98105, USA
Clin Cancer Res 11:2747-55. 2005..Few such data for pediatric glioma lines, particularly those from low-grade tumors, are currently available...
Human glioma cell sensitivity to the sequence-specific alkylating agent methyl-lexitropsinMichael S Bobola
Department of Neurological Surgery, University of Washington, Seattle, WA 98105, USA
Clin Cancer Res 13:612-20. 2007..Our purpose is to characterize the sensitivity of human glioma cells to methyl-lexitropsin (Me-lex), a sequence-specific alkylator that produces 3-methyladenine (3-meA) as the predominant (>90%) DNA lesion...
Minimally cytotoxic doses of temozolomide produce radiosensitization in human glioblastoma cells regardless of MGMT expressionMichael S Bobola
Department of Neurological Surgery, University of Washington, Seattle, WA 98195 6470, USA
Mol Cancer Ther 9:1208-18. 2010..These results provide novel information on which to base further mechanistic study of radiosensitization by temozolomide in human GBM cells and to develop strategies to improve the outcome of concurrent temozolomide radiotherapy...
Apurinic/apyrimidinic endonuclease activity is associated with response to radiation and chemotherapy in medulloblastoma and primitive neuroectodermal tumorsMichael S Bobola
Division of Neurosurgery, Department of Surgery, Children s Hospital and Regional Medical Center, Seattle, WA 98105, USA
Clin Cancer Res 11:7405-14. 2005....
Apurinic/apyrimidinic endonuclease is inversely associated with response to radiotherapy in pediatric ependymomaMichael S Bobola
Department of Neurological Surgery, University of Washington, Seattle, WA 98195 6470, USA
Int J Cancer 129:2370-9. 2011..Our findings support the use of inhibitors of Ap endo activity to overcome resistance...
Apurinic endonuclease activity in adult gliomas and time to tumor progression after alkylating agent-based chemotherapy and after radiotherapyMichael S Bobola
Department of Neurological Surgery, University of Washington, 1959 N.E Pacific Street, Seattle, WA 98195-6470, USA
Clin Cancer Res 10:7875-83. 2004..CONCLUSIONS: Our data suggest that Ap endo activity mediates resistance to alkylating agents and radiation and may be a useful predictor of progression after adjuvant therapy in a subset of gliomas...
The apurinic/apyrimidinic endonuclease activity of Ape1/Ref-1 contributes to human glioma cell resistance to alkylating agents and is elevated by oxidative stressJohn R Silber
Department of Neurological Surgery, University of Washington, Seattle, Washington 98195, USA
Clin Cancer Res 8:3008-18. 2002..Our results may also be relevant to the design of therapeutic regimens using concurrent ionizing radiation (a generator of ROS) and alkylating agent-based chemotherapy...
O6-methylguanine-DNA methyltransferase deficiency in developing brain: implications for brain tumorigenesisMichael S Bobola
Department of Neurological Surgery, Box 356470, University of Washington, Seattle, WA 98195 6470, USA
DNA Repair (Amst) 6:1127-33. 2007..Our findings provide possible mechanistic insight into epidemiologic data associating maternal alkylating agent exposure with brain tumor incidence...
The Werner syndrome protein confers resistance to the DNA lesions N3-methyladenine and O6-methylguanine: implications for WRN functionA Blank
Department of Pathology, University of Washington, Seattle, WA 98195-7705, USA
DNA Repair (Amst) 3:629-38. 2004....
O(6)-methylguanine-DNA methyltransferase in glioma therapy: promise and problemsJohn R Silber
Department of Neurological Surgery, University of Washington, Seattle, WA 98195, USA
Biochim Biophys Acta 1826:71-82. 2012..We conclude by considering approaches that may improve the utility of MGMT methylation status in planning optimal therapies tailored to individual patients...
