Matthew D. Ringel
MD
Professor of Medicine; Director, Thyroid Cancer Research Laboratory
👥Biography 个人简介
Matthew D. Ringel, MD is Professor of Medicine and Director of the Thyroid Cancer Research Laboratory at The Ohio State University (OSU) Comprehensive Cancer Center. He is one of the most influential translational thyroid cancer biologists in the United States, with career-defining contributions to the molecular mechanisms of thyroid cancer invasion, metastasis, and resistance to kinase inhibitor therapy. His laboratory has been continuously funded by the NIH and NCI for over two decades and has trained numerous leaders in thyroid cancer research. Dr. Ringel's research program focuses on the role of BRAF, RAS, and downstream signaling pathways (including PI3K/AKT/mTOR and focal adhesion kinase) in thyroid cancer progression and drug resistance. He identified key mechanisms by which BRAF V600E drives dedifferentiation, invasion, and lymph node metastasis in papillary thyroid cancer, and his work on tumor microenvironment interactions has illuminated how stromal and immune factors modulate thyroid cancer behavior and drug sensitivity. His laboratory has developed murine and cell-based models that have been widely adopted in the field. Beyond basic research, Professor Ringel has translated laboratory discoveries into early-phase clinical trials at OSU. He serves on the American Thyroid Association Thyroid Cancer Guidelines Committee, the NCI Thyroid Cancer Steering Committee, and as editor-in-chief of the journal Thyroid. He has authored over 200 peer-reviewed publications and is a frequent keynote speaker at international thyroid cancer symposia.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
BRAF V600E Signaling in Thyroid Cancer Invasion and Dedifferentiation
Elucidated the molecular mechanisms by which BRAF V600E promotes thyroid cancer cell invasion, epithelial-mesenchymal transition, and loss of thyroid-specific gene expression including sodium-iodide symporter, providing the biological rationale for BRAF-targeted therapy in aggressive differentiated and anaplastic thyroid cancers.
PI3K/AKT/mTOR Pathway in Thyroid Cancer Resistance
Demonstrated that PI3K/AKT/mTOR pathway activation serves as a critical resistance mechanism to BRAF and multi-kinase inhibitors in thyroid cancer, identifying rational combination strategies involving mTOR inhibitors to overcome drug resistance and enhance anti-tumor efficacy.
Tumor Microenvironment and Immune Evasion in Thyroid Cancer
Characterized the immune and stromal composition of the thyroid cancer microenvironment, demonstrating that BRAF V600E signaling suppresses anti-tumor immune responses through PD-L1 upregulation and T-cell exclusion, providing translational rationale for BRAF inhibitor plus immune checkpoint inhibitor combinations.
Representative Works 代表性著作
Activated RIOKinase-2 Is a Mediator of Invasion and Migration in Thyroid Cancer
Oncogene (2011)
Mechanistic study identifying RIOK2 kinase as a novel regulator of thyroid cancer cell invasion and migration downstream of BRAF/MEK signaling, providing a new potential therapeutic target.
The BRAFV600E Mutation Is Associated with Reduced Tumor Lymphocyte Infiltration and Worsened Outcomes in Papillary Thyroid Cancer
Journal of Clinical Endocrinology and Metabolism (2013)
Clinical correlative study linking BRAF V600E status to reduced immune cell infiltration and worse clinical outcomes in papillary thyroid cancer, supporting the tumor-immune microenvironment as a therapeutic target.
Thyroid Cancer, Version 2.2023, NCCN Clinical Practice Guidelines
Journal of the National Comprehensive Cancer Network (2023)
Comprehensive guideline update incorporating emerging targeted and immune therapies for thyroid cancer management, co-authored as part of the NCCN Thyroid Cancer Guidelines Committee.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-04-06 | All information from publicly available academic sources
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