Michael J. Birrer
M.D., Ph.D.
Director, Winthrop P. Rockefeller Cancer Institute; Professor of Medicine
👥Biography 个人简介
Michael Birrer is Director of the Winthrop P. Rockefeller Cancer Institute and Professor of Medicine at the University of Arkansas for Medical Sciences (UAMS). Prior to this role, he led gynecologic cancer research programs at Massachusetts General Hospital/Harvard Medical School and the National Cancer Institute. Birrer is a dual physician-scientist whose research has examined the molecular biology of ovarian cancer with an emphasis on transcription factor signaling — particularly the AP-1 family — and on genomic characterization of ovarian tumors for biomarker and therapeutic target discovery. Birrer contributed to the ARIEL2 trial as an investigator and translational team member, helping analyze genomic predictors of rucaparib response in high-grade serous ovarian cancer. His laboratory discovered that AP-1 transcription factors play critical roles in regulating ovarian cancer cell survival, invasion, and resistance to therapy, providing a mechanistic framework for novel therapeutic targeting approaches. He was also a key participant in landmark TCGA (The Cancer Genome Atlas) analyses of high-grade serous ovarian cancer, contributing to the comprehensive molecular characterization of this disease. Birrer has made substantial contributions to clinical trial design and biomarker science for gynecologic oncology, integrating deep molecular profiling with clinical outcomes across multiple cooperative group and industry trials. He has trained numerous physician-scientists and holds leadership positions in GOG, SGO, and NCI-sponsored research consortia focused on gynecologic malignancies.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
AP-1 Transcription Factor Biology in Ovarian Cancer
Identified and characterized the role of AP-1 transcription factor family members (c-Jun, JunB, c-Fos) in ovarian cancer tumorigenesis, chemotherapy resistance, and invasive behavior, providing novel molecular targets for intervention.
TCGA Genomic Characterization of Ovarian Cancer
Participated in The Cancer Genome Atlas comprehensive genomic characterization of high-grade serous ovarian carcinoma, contributing to the landmark 2011 Nature publication defining the molecular landscape of the disease.
ARIEL2 Translational Research
Contributed to the translational component of the ARIEL2 trial analyzing genomic features — including BRCA mutation, RAD51C/D alterations, and genome-wide loss of heterozygosity — as predictors of rucaparib response.
Biomarker-Driven Clinical Trial Design
Advanced the integration of tumor molecular profiling, including gene expression signatures and somatic mutation analysis, into gynecologic oncology clinical trial design, enabling patient stratification and biomarker validation.
Representative Works 代表性著作
Integrated genomic analyses of ovarian carcinoma (TCGA)
Nature (2011)
Co-authored the landmark TCGA paper presenting comprehensive genomic characterization of 489 high-grade serous ovarian carcinomas, defining mutation spectra, copy-number alterations, methylation patterns, and gene expression subtypes.
ARIEL2 Part 1: identification of low-grade serous ovarian cancer as distinct from high-grade serous ovarian cancer
The Lancet Oncology (2017)
Contributed to translational analyses in ARIEL2 identifying genomic classifiers of rucaparib response, including HRD genomic scar scores and BRCA mutation status, in relapsed platinum-sensitive ovarian cancer.
The role of the AP-1 transcription factor in ovarian cancer
Clinical Cancer Research (2000)
Reviewed evidence implicating AP-1 transcription factor dysregulation in ovarian cancer pathogenesis, resistance mechanisms, and tumor progression, and proposed targeting 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
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