Lauren M. Fishbein

I am a Physician Scientist and Translational Researcher.

Lauren M. Fishbein, M.D., Ph.D.

University of Colorado - Denver

I first read about the promise of the human genome project and its potential for personalized medicine to predict and treat cancer and other diseases when I was a college student in the mid 1990s. I became fascinated with precision medicine and sought to pursue an MD, PhD degree to study cancer genetics.

Lauren Fishbein, MD, PhD, MTR, is an Associate Professor in Medicine at the University of Colorado School of Medicine in the Division of Endocrinology, Metabolism and Diabetes, with a secondary appointment in the Division of Biomedical Informatics and Personalized Medicine. Dr. Fishbein's research and clinical interests are in endocrine neoplasia and tumor genetics, including a special focus on pheochromocytomas and paragangliomas. Pheochromocytomas and paragangliomas are unique tumors that not only can become metastatic but can secrete hormones leading to high morbidity and mortality; interestingly, up to 40% are hereditary, with over 12 well-defined susceptibility genes. Many of these genes are in completely different pathways in the cell and yet create the same histological tumor type. And different susceptibility genes, even within the same protein complex, carry a different penetrance for tumor development and different risk of developing metastatic disease. These were the concepts that intrigued Dr. Fishbein to study pheochromocytoma and paraganglioma as a model of cancer genetics, to understand the interplay between germline and somatic genetics. Her research program works towards understanding the impact and implication of germline predisposition genetics, as well as understanding tumor development and transformation to aggressive and metastatic disease. One current project funded by the NCI is to identify genetic risk modifiers for penetrance of disease in the Hereditary Paraganglioma-Pheochromocytoma Syndromes.


Grant Listing
Project Title Grant Number Program Director Publication(s)
Inherited genetic variation and penetrance of Hereditary Paraganglioma-Pheochromocytoma Syndrome
1R01CA246586-01A1
Melissa Rotunno


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Last Updated: 01/06/2021 11:57:21