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Translational Medicine / 转化医学Cancer Stem Cells

Kornelia Polyak

科内利亚·波利亚克

MD, PhD

🏢Dana-Farber Cancer Institute / Harvard Medical School(丹娜-法伯癌症研究所 / 哈佛医学院)🌐USA

Professor of Medicine, Harvard Medical School; Senior Scientist, Dana-Farber Cancer Institute哈佛医学院医学教授;丹娜-法伯癌症研究所高级科学家

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h-index
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Key Papers
5
Awards
3
Key Contributions

👥Biography 个人简介

Kornelia Polyak, MD PhD at Dana-Farber/Harvard is a world authority on breast cancer heterogeneity, CSC markers, and clonal evolution. Her lab dissects the cellular and molecular diversity within breast tumors, characterizes CSC populations using markers such as CD44/CD24/ALDH1, and investigates how tumor-stromal interactions and clonal dynamics drive breast cancer progression from in situ to invasive disease.

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🧪Research Fields 研究领域

Breast Cancer Heterogeneity乳腺癌异质性
Cancer Stem Cell Markers癌症干细胞标志物
Clonal Evolution克隆进化
Tumor Microenvironment肿瘤微环境
DCIS to Invasive Transition原位癌至浸润癌转变

🎓Key Contributions 主要贡献

Breast Cancer Heterogeneity and CSC Subpopulations

Used single-cell genomics and flow cytometry to demonstrate that breast tumors contain functionally distinct subpopulations with varying tumor-initiating capacities, and showed that CD44+/ALDH1+ cells are enriched for CSC activity and metastatic potential.

Clonal Evolution in Breast Cancer

Applied whole-genome sequencing of single cells and microdissected tumor regions to reconstruct clonal evolutionary trees in breast cancer, revealing parallel evolution, convergent mutations, and non-linear branching patterns.

DCIS to Invasive Breast Cancer Transition

Investigated the cellular and microenvironmental determinants of progression from ductal carcinoma in situ (DCIS) to invasive breast cancer, identifying myoepithelial cell dysfunction and immune infiltration as key determinants of invasion.

Representative Works 代表性著作

[1]

A cancer cell program promotes T cell exclusion and resistance to checkpoint blockade

Cell (2019)

Identified a cancer cell-intrinsic program that drives immunosuppression in breast tumors by excluding T cells, linking CSC states to immune evasion.

[2]

Functional and genetic analysis of chromatin accessibility identifies breast cancer vulnerability

Nature Genetics (2018)

Combined ATAC-seq and scRNA-seq to map chromatin accessibility in breast CSC subpopulations, identifying epigenetic vulnerabilities specific to tumor-initiating cells.

[3]

Clonal evolution in breast cancer revealed by single nucleus genome sequencing

Nature (2014)

Used single-nucleus sequencing to reconstruct clonal architecture and evolutionary dynamics within individual breast tumors, revealing complex branching evolution.

🏆Awards & Recognition 奖项与荣誉

🏆Elected Member, National Academy of Medicine
🏆AACR Award for Outstanding Achievement in Cancer Research
🏆Susan G. Komen Foundation Scholar Award
🏆Breast Cancer Research Foundation Investigator Award
🏆BCRF-Phi Beta Psi Translational Award

📄Data Sources 数据来源

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

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