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Sean Morrison

肖恩·莫里森

PhD

🏢UT Southwestern Medical Center(德克萨斯大学西南医学中心)🌐USA

Director, Children's Research Institute; Mary McDermott Cook Chair in Pediatric Genetics儿童研究所所长;小儿遗传学玛丽·麦克德莫特·库克讲席教授

85
h-index
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Key Papers
4
Awards
3
Key Contributions

👥Biography 个人简介

Sean Morrison, PhD directs the Children's Research Institute at UT Southwestern and is a Howard Hughes Medical Institute Investigator. His lab demonstrated that melanoma does not follow a strict CSC hierarchy and that oxidative stress is a key vulnerability for metastasizing melanoma cells. He also showed that antioxidants promote melanoma metastasis, with major implications for cancer prevention.

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🧪Research Fields 研究领域

Melanoma Stem Cells黑色素瘤干细胞
Neural Crest Biology神经嵴生物学
Oxidative Stress Resistance氧化应激抗性
Metastasis转移
Hematopoietic Stem Cells造血干细胞

🎓Key Contributions 主要贡献

Challenging the Strict CSC Hierarchy Model in Melanoma

Showed that in optimized xenograft conditions, virtually all melanoma cells can form tumors, challenging the notion of a rare CSC population and demonstrating high phenotypic plasticity in melanoma.

Oxidative Stress and Melanoma Metastasis

Demonstrated that metastasizing melanoma cells face lethal oxidative stress and must upregulate antioxidant defenses to survive, identifying ferroptosis vulnerability and showing that antioxidants paradoxically promote metastasis.

Neural Crest and Melanocyte Stem Cell Biology

Elucidated mechanisms regulating neural crest stem cell self-renewal and differentiation, providing a developmental framework for understanding melanoma cell-of-origin and tumor initiation.

Representative Works 代表性著作

[1]

Melanoma Originates from Cells with a Neural-Crest Gene Signature and Undergoes Phenotypic Switching

Nature (2008)

Demonstrated high frequency of tumor-initiating cells in melanoma under improved xenograft conditions, reshaping understanding of melanoma CSC hierarchy.

[2]

Antioxidants stimulate BACH1-dependent tumor angiogenesis

Nature (2019)

Revealed that antioxidants promote melanoma metastasis by reducing oxidative stress on circulating tumor cells, with implications for clinical use of antioxidant supplements.

[3]

Oxidative stress inhibits distant metastasis by human melanoma cells

Nature (2015)

Showed metastasizing melanoma cells must withstand elevated oxidative stress, identifying a metabolic vulnerability exploitable therapeutically.

🏆Awards & Recognition 奖项与荣誉

🏆Howard Hughes Medical Institute Investigator
🏆Elected Member, National Academy of Sciences
🏆Elected Member, National Academy of Medicine
🏆AACR G.H.A. Clowes Award

📄Data Sources 数据来源

Last updated: 2026-01-15 | All information from publicly available academic sources

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