Stephen J. Meltzer
斯蒂芬·梅尔策
MD
Loeb Professor of Gastroenterology; Professor of Oncology and Medicine; Co-Director, GI Cancer Research洛布讲席教授;肿瘤学与内科学教授;胃肠肿瘤研究联合主任
👥Biography 个人简介
Stephen J. Meltzer, MD is the Loeb Professor of Gastroenterology and Professor of Oncology and Medicine at the Johns Hopkins University School of Medicine, where he co-directs gastrointestinal cancer research. He is one of the world's preeminent molecular biologists studying the progression from Barrett's esophagus (BE) to esophageal adenocarcinoma (EAC)—a field he has shaped over three decades through foundational discoveries in epigenetic alterations, microRNA regulation, and DNA methylation biomarkers that drive neoplastic transformation. Meltzer's laboratory was among the first to characterize genome-wide methylation abnormalities in BE and EAC, identifying candidate epigenetic biomarkers for early detection that have entered clinical evaluation. He contributed groundbreaking work identifying p16 (CDKN2A) hypermethylation as an early molecular event in BE-to-EAC progression, and his translational research pipeline has produced multiple DNA methylation and microRNA-based biomarker assays for risk stratification of patients with Barrett's esophagus under endoscopic surveillance. Beyond epigenetics, Meltzer has contributed to the molecular characterization of EAC genomics, studied the mechanisms of photodynamic therapy and endoscopic ablative techniques for early esophageal neoplasia, and developed predictive models for progression from non-dysplastic Barrett's to high-grade dysplasia and invasive cancer. He has been continuously funded by the National Institutes of Health for over 25 years and has authored over 300 peer-reviewed publications. His work provides the molecular foundation for endoscopic surveillance protocols and early intervention strategies in Barrett's esophagus.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
Epigenetic Biomarkers for Barrett's Esophagus and Early EAC Detection
Pioneered identification and validation of DNA methylation biomarkers (including p16/CDKN2A, RUNX3, HPP1) in Barrett's esophagus biopsies as risk stratification tools for dysplasia and adenocarcinoma progression, establishing the epigenetic framework for early EAC detection.
MicroRNA Profiling in Esophageal Cancer Progression
Performed landmark microRNA expression profiling studies characterizing microRNA alterations during BE-to-EAC progression, identifying miR-192 and other regulatory microRNAs as markers of disease progression and potential therapeutic targets.
Genome-Wide Methylation Mapping in EAC and Barrett's
Led comprehensive genome-wide methylation studies that mapped the epigenetic landscape of EAC and its precursors, defining the methylome of Barrett's esophagus and creating reference datasets used by laboratories worldwide for translational biomarker research.
Endoscopic Molecular Biomarkers for Surveillance Optimization
Translated epigenetic discoveries into clinical-grade molecular biomarker assays applicable to endoscopic surveillance biopsy specimens, enabling risk stratification beyond standard histopathology and supporting reduced surveillance intervals in low-risk patients.
Representative Works 代表性著作
Methylation of CDKN2A and loss of heterozygosity on 9p21 in Barrett's esophagus
Journal of the National Cancer Institute (2001)
Landmark study demonstrating that epigenetic silencing of p16/CDKN2A by methylation is an early and frequent event in Barrett's metaplasia, establishing a key molecular step in esophageal adenocarcinoma progression.
MicroRNA expression profiles of human stomach and esophageal adenocarcinomas
International Journal of Cancer (2006)
First comprehensive microRNA profiling of esophageal and gastric adenocarcinomas, identifying cancer-specific microRNA signatures and dysregulated oncomiRs and tumor suppressor microRNAs with functional implications.
Comprehensive molecular characterization of gastro-oesophageal adenocarcinoma
Nature (2017)
TCGA consortium paper (co-authored) providing integrative genomic, epigenomic, transcriptomic and proteomic characterization of esophageal and gastric adenocarcinoma, defining molecular subtypes with therapeutic relevance.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-01-15 | All information from publicly available academic sources
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