Biography
Dr. Okimoto is a medical oncologist who specializes in the treatment of sarcomas and lung cancer. He is a laboratory based physician-scientist who broadly aims to translate basic science discoveries into novel therapies for patients with cancer. He is currently interested in understanding how cancer cells gain transcriptional dependence to drive tumor progression and metastasis.
Education
Education
Creighton University School of Medicine 2009
Residencies
Tufts Medical Center, Internal Medicine 2012
Board Certifications
American Board of Internal Medicine
American Board of Internal Medicine, Medical Oncology
Awards & Honors
Award | Conferred By | Date |
---|---|---|
Damon Runyon Clinical Investigator Award Finalist | 2021 | |
National Cancer Institute R37 MERIT Award | 2021 | |
American Society of Clinical Investigation Young Physician-Scientist Award | 2019 | |
NIH-NCI Career Development Award (K08) | 2018 | |
UCSF DOM Cohort Iniative Award | 2018 | |
A.P. Giannini Postdoctoral Fellowship | 2015 |
Clinical Expertise
Pulmonary Metastases
Soft Tissue Sarcoma
Bone Sarcoma
Grants and Funding
- Therapeutic degradation of Capicua (CIC) fused oncoproteins in undifferentiated sarcomas | NIH | 2021-06-17 - 2026-05-31 | Role: Principal Investigator
- Therapeutic rescue of the transcriptional repressor Capicua to inhibit lung cancer metastasis | NIH | 2018-02-01 - 2023-01-31 | Role: Principal Investigator
Research Narrative
A physician-scientist, Okimoto conducts research in addition to providing clinical care. The overall goal of his laboratory-based investigations is to help improve outcomes for cancer patients. His current research work focuses on understanding the molecular mechanisms that promote tumor cell metastasis.
Publications
MOST RECENT PUBLICATIONS FROM A TOTAL OF 43
- A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States.| | PubMed
- Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.| | PubMed
- Mytilus mitochondrial DNA contains a functional gene for a tRNASer(UCN) with a dihydrouridine arm-replacement loop and a pseudo-tRNASer(UCN) gene.| | PubMed