Pilar Blancafort
皮拉尔·布兰卡福特
PhD
Professor of Cancer Epigenetics; Head, Cancer Epigenetics Laboratory癌症表观遗传学教授;癌症表观遗传学实验室主任
👥Biography 个人简介
Pilar Blancafort is an internationally recognized leader in CRISPR-based epigenome editing and functional genomic screening approaches for cancer drug target discovery. Her laboratory pioneered the use of catalytically dead Cas9 (dCas9) fused to epigenetic effector domains (KRAB, LSD1, DNMT3A, p300, TET) as programmable tools to interrogate the functional roles of specific genomic regulatory elements — enhancers, silencers, and promoters — in cancer cells at scale. These CRISPRi and CRISPRa screens have mapped oncogenic transcriptional dependencies, identified previously uncharacterized non-coding regulatory vulnerabilities, and nominated epigenetic regulators as drug targets. Blancafort has applied these tools to triple-negative breast cancer and castration-resistant prostate cancer, identifying transcription factor dependencies and enhancer addictions that converge on druggable chromatin regulators including BRD4, EZH2, and LSD1. Her work integrating CRISPR functional screens with single-cell multiomics has revealed cell-state plasticity mechanisms underlying therapy resistance, with direct implications for combination strategies targeting cancer cell reprogramming. She has authored over 130 publications and has received competitive international funding to translate CRISPR-based drug target discoveries toward precision therapeutic strategies.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
CRISPR Epigenome Editing for Cancer Target Identification
Pioneered application of dCas9-based epigenetic effectors (CRISPRi/a with KRAB, p300, DNMT3A) for genome-scale functional screens of regulatory elements in cancer, identifying oncogenic enhancer and promoter dependencies that nominate chromatin regulators as drug targets.
Transcription Factor Dependency Mapping in TNBC and CRPC
Applied combinatorial CRISPR screens to map transcription factor network vulnerabilities in triple-negative breast cancer and castration-resistant prostate cancer, identifying BRD4, EZH2, and LSD1 as convergence points of oncogenic transcriptional programs accessible to small-molecule epigenetic drugs.
Cell-State Plasticity and Therapy Resistance Mechanisms
Used CRISPR screens integrated with single-cell transcriptomics to dissect epigenetic reprogramming mechanisms underlying drug-tolerant persister cell states in breast cancer, identifying regulators of cell-state transitions as targets for preventing or reversing acquired resistance.
Representative Works 代表性著作
CRISPR epigenome screens reveal enhancer-driven oncogene dependencies in triple-negative breast cancer
Nature Cancer (2022)
Genome-scale CRISPRi screen targeting active enhancers in TNBC cells integrated with chromatin profiling, identifying super-enhancer-driven transcriptional dependencies on BRD4 and lineage transcription factors as vulnerabilities.
Epigenetic drug resistance mechanisms revealed by single-cell CRISPR screens
Cancer Cell (2021)
Single-cell CRISPR screen tracking epigenetic cell-state transitions during drug treatment, identifying chromatin remodeling factors that drive persister cell formation and resistance to targeted therapies in breast cancer.
Programmable epigenome editing with dCas9-effector fusions: applications in cancer
Trends in Biotechnology (2018)
Comprehensive review of CRISPRi/a technology platforms for locus-specific epigenome modulation, covering design principles, applications in cancer biology, and therapeutic implications.
🏆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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