CHARLES KELLER, M.D.
Adjunct Scientist, Legacy Research Institute
Phone: 801-232-8038 | Email: firstname.lastname@example.org
Charles’ research focuses on the development of more effective, less toxic therapies for childhood cancers. His special interest is advanced disease that has spread beyond the initial location of the cancer or which makes the tumor unresectable. Charles has co-chaired the brain tumor developmental therapeutics committee (CNS-DVL) of the Children’s Oncology Group and is a member of the soft tissue sarcoma (STS) committee of Children’s Oncology Group. He has also regularly been a standing or ad hoc member of NIH/NCI Study Sections.
Charles attended Tulane University where he received a degree in Biomedical Engineering prior to attending Baylor College of Medicine where he received his M.D. degree. After completing his internship and residency in Pediatrics at Texas Children’s Hospital, Charles trained in Pediatric Hematology-Oncology at the University of Utah and with 2007 Nobel laureate, Mario Capecchi. Charles has authored over 100 scientific publications and is a recognized expert in the biology of childhood sarcomas and the preclinical investigation of childhood cancers.
Charles is also a co-founder of First Ascent Biomedical (a company developing personalized medical approaches to therapy for canine and human solid tumor patients), Artisan Biopharma (a company helping translate drug discoveries to clinical use), and Tio Companies that improves drug safety and cancer drug effectiveness*. In their spare time, Charles, his wife Kelly & their daughters enjoy outdoor adventures, as well as designing and building treehouses and Japanese Teahouses.
* overlap between cc-TDI, FirstAscent, Artisan Biopharma and Tio Companies is overseen by a conflict of interest management committee.
In vitro benchmarking of NF-κB inhibitors.
Interleukin-4 receptor inhibition targeting metastasis independent of macrophages.
SMARCA4-miR27a axis promotes expression of the PAX3:FOXO1 fusion oncogene in rhabdomyosarcoma.
IGF1R as a Key Target in High Risk, Metastatic Medulloblastoma.
Functionally-defined Therapeutic Targets in Diffuse Intrinsic Pontine Glioma.
Lineage of Origin in Rhabdomyosarcoma informs Pharmacological Response.
As a physician-scientist, my laboratory has been devoted to the development of novel molecular therapies for advanced childhood cancers (sarcomas and brain tumors) associated with high morbidity or mortality. The long-term emphasis of my laboratory’s research is molecularly-targeted therapies to halt progression or induce regression for gross residual disease, metastatic disease and relapsed disease.
To achieve these goals, my laboratory has traditionally utilized physiologically-accurate, genetically-engineered mouse models (GEMMs) of soft tissue sarcomas including alveolar & embryonal rhabdomyosarcoma, and brain tumors including medulloblastoma. In parallel, we also develop primary tumor cell cultures of pediatric cancers for preclinical validation studies. Our approach has been to study these childhood cancers in the context of developmental biology. By providing the scientific community a centralized knowledge base and experimental resources of validated and credentialed models, we hope to recruit not only cancer biologists but also developmental biologists, cancer biologists and engineers to the investigation of these devastating childhood cancers.
Collaborations with cancer biologists and neuroscientists at Legacy Research Institute and clinicians at the Randall Children’s Hospital at Legacy Emanuel bolster our shared mission to discover more effective treatments for these children whose lives have been touched by cancer.