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Philip Bernstein

菲利普·伯恩斯坦

MD, PhD

🏢University of Rochester Medical Center(罗切斯特大学医学中心)🌐USA

Professor of Radiation Oncology; Director, Center for RNA Biology放射肿瘤学教授;RNA生物学中心主任

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h-index
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Key Papers
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Awards
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Key Contributions

👥Biography 个人简介

Philip Bernstein has made foundational contributions to the mechanistic understanding and clinical application of PARP inhibitors as radiosensitizers. His research group has systematically characterized how PARP1/2 inhibition potentiates radiation-induced DNA damage by blocking base excision repair and single-strand break repair, converting these lesions into cytotoxic double-strand breaks during DNA replication. His work has been instrumental in the clinical development of PARP inhibitor–radiation combination strategies for glioblastoma, pancreatic cancer, and other solid tumors.

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🧪Research Fields 研究领域

PARP InhibitorsPARP抑制剂
Radiosensitization放射增敏
DNA Repair InhibitionDNA修复抑制
Synthetic Lethality合成致死
Homologous Recombination Deficiency同源重组缺陷
Combination Radiation Therapy联合放射治疗

🎓Key Contributions 主要贡献

PARP1 Mechanism of Radiosensitization

Demonstrated that PARP1 inhibition prevents repair of single-strand breaks induced by radiation, leading to DSB formation at replication forks and pronounced cell killing in S-phase cells—establishing the mechanistic rationale for PARP inhibitor + radiation combinations.

Tumor Selective Radiosensitization

Showed that HR-deficient tumor cells are disproportionately sensitized by PARP inhibition combined with radiation, providing a therapeutic window for clinical translation in BRCA-mutant and BRCAness cancers.

Clinical Translation

Conducted preclinical studies supporting multiple phase I/II trials combining olaparib, niraparib, and other PARP inhibitors with radiotherapy in glioblastoma and gastrointestinal cancers.

Representative Works 代表性著作

[1]

PARP inhibition enhances radiation sensitivity through trapping of PARP1 at double-strand breaks

Cancer Research (2019)

Mechanistic study clarifying that PARP trapping, not merely catalytic inhibition, is the primary driver of radiation sensitization.

[2]

Potentiation of radiation response in human cancer cells by a novel inhibitor of poly(ADP-ribose) polymerase

International Journal of Radiation Oncology Biology Physics (2009)

Proof-of-concept study demonstrating marked radiosensitization by PARP inhibition across multiple human cancer cell lines.

[3]

Olaparib combined with radiotherapy for newly diagnosed glioblastoma: preclinical mechanistic rationale and phase I trial

Clinical Cancer Research (2022)

Translational study bridging PARP inhibitor radiosensitization from bench to the first clinical trial in GBM.

🏆Awards & Recognition 奖项与荣誉

🏆American Cancer Society Research Scholar Award
🏆NIH R01 Merit Award
🏆ASTRO Basic Science Award
🏆Radiation Research Society Annual Meeting Award

📄Data Sources 数据来源

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

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