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Junjie Chen

陈俊杰

PhD

🏢The University of Texas MD Anderson Cancer Center(德克萨斯大学MD安德森癌症中心)🌐USA

Professor and Chair, Department of Experimental Radiation Oncology实验放射肿瘤学系教授兼系主任

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Key Papers
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Awards
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Key Contributions

👥Biography 个人简介

Junjie Chen is a world-leading expert in DNA damage response and double-strand break repair. His laboratory at MD Anderson has made seminal contributions to understanding how cells choose between NHEJ and homologous recombination repair pathways after ionizing radiation. He discovered key regulatory mechanisms involving ATM kinase activation, 53BP1, and BRCA1 that govern DSB repair pathway selection, work that has profoundly shaped our understanding of radiation sensitivity and resistance in cancer cells.

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🧪Research Fields 研究领域

DNA Damage ResponseDNA损伤反应
DNA Double-Strand Break RepairDNA双链断裂修复
NHEJ vs HR Pathway ChoiceNHEJ与HR通路选择
ATM/ATR Kinase SignalingATM/ATR激酶信号
BRCA1/2 FunctionBRCA1/2功能
Radiation Biology放射生物学

🎓Key Contributions 主要贡献

DSB Repair Pathway Choice

Elucidated the molecular antagonism between 53BP1 and BRCA1 that determines whether cells use NHEJ or HR to repair radiation-induced double-strand breaks, explaining differential radiosensitivity between cell types.

ATM Kinase Signaling Network

Mapped the ATM-dependent phosphorylation cascade triggered by ionizing radiation, identifying hundreds of substrates and revealing how the DNA damage checkpoint coordinates repair with cell cycle arrest.

Radiosensitization Targets

Identified synthetic lethal interactions between HR deficiency and PARP inhibition that can be exploited to sensitize tumors with BRCA mutations to radiation therapy.

Representative Works 代表性著作

[1]

53BP1 inhibits homologous recombination in Brca1-deficient cells by blocking resection of DNA breaks

Cell (2010)

Landmark study demonstrating the molecular basis for 53BP1/BRCA1 antagonism in DSB repair pathway choice, highly cited in radiation biology.

[2]

ATM substrate analysis reveals extensive protein networks responsive to DNA damage

Science (2007)

Comprehensive proteomics study mapping the ATM-dependent phosphoproteome after ionizing radiation exposure.

[3]

RNF8 ubiquitylates histones at DNA double-strand breaks and promotes assembly of repair proteins

Cell (2007)

Identified ubiquitin-mediated chromatin remodeling as essential for recruiting repair factors to DNA damage sites.

🏆Awards & Recognition 奖项与荣誉

🏆AACR Outstanding Investigator Award
🏆Radiation Research Society Michael Fry Award
🏆American Society for Radiation Oncology (ASTRO) Basic Science Award
🏆NCI Outstanding Investigator Award

📄Data Sources 数据来源

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

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