IMPORTANT UPDATE – As of 10/22/2020, Challen Lab's research activities are operating at limited capacity in accordance with Washington University's guidelines to help slow the spread of SARS-CoV2
Department of Medicine - Oncology Division - Molecular Oncology Section
Dr. Challen's work in understanding the molecular regulation of hematopoietic stem cells is motivated by his desire to improve the lives of patients afflicted with hematopoietic disorders. His ultimate career goal is to see the implementation of meaningful discoveries in basic biology help drive novel clinical outcomes...
Join Our Team!
Challen Lab actively recruits motivated and enthusiastic post-docs, Ph.D. students and technicians to work and assist on projects related to stem cells, epigenetics and leukemia research!
Challen Lab trainees have a 100% success rate for acquiring awards and fellowships!
Please send CV/resume, references, and research statements to Dr. Grant Challen – email@example.com
For more info on Challen Lab positions, please visit https://jobs.wustl.edu/ and search 'Challen'
To learn more about our team, please visit our Lab Members page!
Challen Lab Research
Hematopoietic stem cells (HSCs) reside in the bone marrow and are defined by their capacity for lifetime maintenance of the blood and bone marrow, achieved through their differentiation into the myriad of cellular components, as well as their ability to generate additional stem cells via self-renewal. The mechanisms that instruct the fate of stem cells toward differentiation versus self-renewal are still relatively poorly understood. A number of transcription factors have been identified as critical for HSC maintenance and self-renewal; however, we have little insight into how these factors are orchestrated by epigenetic mechanisms to ensure blood homeostasis. The central theme of the Challen Lab's research is understanding how epigenetic marks such as histone methylation and acetylation, DNA methylation, and 5-hydroxymethylation co-ordinately act to regulate normal HSC function and how these processes go awry in hematopoietic diseases such as leukemia and lymphoma. In order to explore these questions, we use various mouse genetic models to study the roles of genetic mutations of different components of the epigenetic machinery in cancers of the blood and bone marrow.