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Experimental Approaches to Unravel Ferroptosis: Strategies and Tools for Deciphering Regulated Cell Death
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Chao-Chieh Lin

Chao-Chieh Lin

Department of Molecular Genetics and Microbiology, Duke University School of Medicine

Dr. Chao-Chieh Lin earned his PhD in genetics and genomics from Duke University. He is currently a senior research associate in the Department of Molecular Genetics & Microbiology at Duke University School of Medicine. His research focuses on the molecular mechanisms of ferroptosis and their implications in cancer, neurodegeneration, and stroke. He has published 20 peer-reviewed articles in leading journals such as Journal of Clinical Investigation, Cell Death & Differentiation, Nature Communications, EMBO Reports, and Oncogene. Dr. Lin’s work has uncovered novel regulators of ferroptosis, therapeutic compounds, and protective pathways with significant translational potential for human health.

Collection Overview

Ferroptosis is a regulated form of cell death driven by iron-dependent lipid peroxidation. Over the past decade, it has emerged as a fundamental biological process with wide-ranging implications in cancer, neurodegeneration, ischemia-reperfusion injury, and immunology. Despite its growing importance, the field is limited by a lack of standardized methods and reproducible protocols that enable researchers to detect, induce, and modulate ferroptosis across different model systems.


This Methods Collection aims to assemble a set of practical, validated approaches for studying ferroptosis, spanning chemical and genetic tools, lipidomics workflows, cell-based assays, and in vivo models. By gathering diverse methodologies in a centralized resource, this collection will provide researchers with a toolkit to rigorously dissect ferroptosis mechanisms and apply them in biomedical contexts.


This collection will help the research community by promoting consistency, comparability, and innovation in ferroptosis research. It will also highlight emerging technologies that can accelerate translation of ferroptosis biology into therapeutic strategies, making it a valuable reference for established investigators and new entrants to the field.

Articles

A Ferric Ammonium Citrate-Based Model of Iron Overload With Ferroptosis-Associated Readouts In C2C12 Myoblasts

A Ferric Ammonium Citrate-Based Model of Iron Overload With Ferroptosis-Associated Readouts In C2C12 Myoblasts

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2026

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