Andrew Arnold, M.D.Murray-Heilig Chair in Molecular Medicine
Professor of Medicine and Genetics and Genome Sciences
Director, Center for Molecular Oncology
Chief, Division of Endocrinology and Metabolism
Director, Office of Physician-Scientist Career Development
Pathogenesis of parathyroid and other endocrine tumors, and role of the cyclin D1 oncogene in neoplasia, including breast cancer.
|No data available|
|Residency||University of Chicago||Internal Medicine|
|Fellowship||National Cancer Institute/NIH||Molecular Oncology|
|Fellowship||Massachusetts General Hospital||Medicine, Endocrinology|
|Name of Award/Honor||Awarding Organization|
|Refer to Abbreviated CV Link|
Parathyroid disorders; genetic/inherited endocrine tumor syndromes
The most longstanding interest of our laboratory has been in the molecular genetic underpinnings of tumors of the endocrine glands. It was in the context of a search for a parathyroid tumor oncogene lying adjacent to a clonal chromosomal breakpoint that we discovered cyclin D1 (PRAD1). Cyclin D1 has proven to play a key role in cell cycle regulation, and has emerged as a major human oncogene, important in multiple types of tumors including breast cancer and B-cell lymphoma. We are currently pursuing a number of approaches, including the use of transgenic mouse models, to learn more about the precise mechanisms by which cyclin D1 exerts its oncogenic effects. In addition to the cyclin D1 work, we are continuing a major initiative seeking additional genes that contribute to endocrine neoplasia. In this context, we identified the HRPT2 gene as a major factor in the development of malignant parathyroid tumors, a finding that carries important clinical implications.
Accepting students for Lab Rotations: Summer '17, Fall '17, Spring '18