Yoon-Jae Cho
MD
Associate Professor, Department of Neurology; Knight Cancer Institute Member; Director, Pediatric Brain Tumor Program, Doernbecher Children's Hospital
👥Biography 个人简介
Yoon-Jae Cho, MD is Associate Professor in the Department of Neurology at Oregon Health & Science University (OHSU), a member of the Knight Cancer Institute, and Director of the Pediatric Brain Tumor Program at Doernbecher Children's Hospital. He is one of the leading researchers in medulloblastoma biology, known for significant contributions to the molecular subgroup classification of medulloblastoma—particularly the WNT and SHH subgroups—and for translational work identifying therapeutic vulnerabilities within these subgroups. His research integrates genomics, epigenomics, and developmental neurobiology to understand medulloblastoma pathogenesis. Dr. Cho performed much of his foundational research as a postdoctoral fellow and junior investigator at Stanford University and the Children's Hospital Boston/Dana-Farber Cancer Institute, where he participated in landmark studies characterizing the four major medulloblastoma subgroups (WNT, SHH, Group 3, Group 4) using gene expression profiling and DNA methylation data from large international consortia. His subsequent independent work at OHSU has focused on understanding the developmental cell-of-origin for specific subgroups and identifying subgroup-specific driver mechanisms—including MYC amplification in Group 3 and SMO/PTCH alterations in SHH-subgroup tumors—as targets for therapy. Beyond subgroup classification, Dr. Cho's laboratory investigates epigenetic mechanisms of medulloblastoma pathogenesis and resistance, including the role of chromatin-remodeling complexes and histone modifications. He has contributed to clinical trial design for subgroup-stratified risk reduction in WNT-subgroup medulloblastoma—which has a favorable prognosis—and therapeutic intensification for Group 3 tumors with poor outcomes. His program at OHSU is expanding the use of patient-derived organoids and mouse models for preclinical drug development in medulloblastoma.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
Medulloblastoma Molecular Subgroup Classification (WNT, SHH, Group 3, Group 4)
Contributed to the landmark international consensus studies defining four core molecular subgroups of medulloblastoma through integrative gene expression and DNA methylation analysis, each with distinct biology, demographics, and prognosis—forming the basis of the current WHO classification and clinical risk stratification.
WNT Subgroup Biology and Therapy De-escalation
Investigated the developmental origins and molecular mechanisms of WNT-subgroup medulloblastoma, demonstrating that WNT pathway activation confers exceptional sensitivity to standard therapy and supporting rational treatment de-escalation trials to reduce late effects in this favorable-prognosis subgroup.
SHH Pathway Biology and SMO/PTCH Targeting
Characterized SHH-subgroup medulloblastoma driver alterations including PTCH1 mutations, SMO mutations, and SUFU deletions, and contributed to understanding of SMO inhibitor resistance mechanisms and alternative SHH pathway activation at downstream nodes.
Epigenomic Mechanisms in Medulloblastoma
Investigated chromatin remodeling and epigenetic regulation as drivers of subgroup identity and treatment resistance in medulloblastoma, identifying potential epigenetic targets such as EZH2 and BET bromodomains as tractable vulnerabilities in high-risk subgroups.
Representative Works 代表性著作
Medulloblastoma comprises four distinct molecular variants
Journal of Clinical Oncology (2011)
Definitive multi-institutional study establishing consensus four-subgroup model (WNT, SHH, Group 3, Group 4) of medulloblastoma using gene expression profiling of 550 tumors, demonstrating highly distinct clinical and molecular features across subgroups.
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia (contribution to international consortium medulloblastoma studies)
Nature Genetics (2012)
Co-authored landmark medulloblastoma genomic landscape study using whole-genome sequencing of 125 tumors to identify subgroup-specific somatic mutations, structural variants, and copy number alterations driving each molecular subgroup.
Identification of pre-existing and acquired resistance mechanisms to Hedgehog pathway inhibition in medulloblastoma
Cancer Discovery (2013)
Study characterizing mechanisms of primary and acquired resistance to smoothened inhibitors in SHH-subgroup medulloblastoma, including downstream pathway reactivation via Gli2 amplification and PI3K pathway activation.
Subgroup-specific prognostic implications of TP53 mutation in medulloblastoma
Journal of Clinical Oncology (2013)
Demonstrated that TP53 mutations are specifically associated with ultra-high-risk outcomes in the SHH subgroup of medulloblastoma, providing a molecular rationale for subgroup-specific intensification strategies.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-04-05 | All information from publicly available academic sources
Related Experts 相关专家
Antoni Ribas
UCLA Jonsson Comprehensive Cancer Center
Drew M. Pardoll
Johns Hopkins University
Padmanee Sharma
MD Anderson Cancer Center
Naiyer A. Rizvi
Columbia University Irving Medical Center
关注 Yoon-Jae Cho 的研究动态
Follow Yoon-Jae Cho's research updates
留下邮箱,当我们发布与 Yoon-Jae Cho(Oregon Health & Science University (OHSU))相关的新研究或访谈时,我们会通知你。
Explore More Experts
Discover the researchers shaping the future of cancer treatment