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Washington University in St. Louis School of Medicine Division of Biology and Biomedical Sciences Division of Biology and Biomedical Sciences
Division of Biology and Biomedical Sciences Division of Biology and Biomedical Sciences
Keith M. Rich, M.D.

Associate Professor
Neurological Surgery
Anatomy and Neurobiology
Radiology
Neurosciences Program
Molecular Cell Biology Program
Developmental Biology Program
Lab Phone: 314-362-3694
Other Phone:
FAX: 314-362-2107
Box: 8057
Lab Address: 516 McMillan Building
Email: rich_k@wustl.edu
Keywords: apoptosis; cancer; DNA damage; glioma; gene expression
Research Abstract:
The primary area of investigation in our laboratory is the role of apoptosis after exposure of glioma cells to DNA-damaging agents in the treatment of brain tumors. We are correlating p53 and bcl-2 family gene expression in human glioma cell lines. More recently we have expanded studies to models of death in glioma cells. Methods include a variety of histological, cell culture, and fluorescent cell staining techniques. In vitro studies evaluate agents that influence neuronal or glioma cell death in a bioassay.

Selected Publications:
Vogelbaum MA, Tong JX, Perugu R, et al. Overexpression of BAX in human glioma cell lines. J Neurosurg 1999 91:483-489.

Vogelbaum MA, Tong JX, Higashikubo R, et al. Transfection of C6 glioma cells with the bax gene results in increased sensitivity to treatment with cytosine arabinoside. J Neurosurg 1998 88(1):99-105.

Vogelbaum MA, Tong JX, Rich KM. Developmental regulation of apoptosis in dorsal root ganglion neurons. J Neurosci 1998 18(21):8928-8935.

Rich KM, Tong JX. Flunarizine enhances survival and regeneration after sensory and motor peripheral nerve injury. Restor Neurol Neurosci 1997 11:203-209.

Tong JX, Vogelbaum MA, Rich KM. Radiation-induced apoptosis in dorsal root ganglions. J Neurocytol 1997 26:771-777.