Highlights
- 1Nature biotechnology · 2022KCKevan ChuLELukas Edward Dow
- 2
- 3
Publications
Funding
Active
8 grants- PIR01CA297721-02Mechanisms of genetic and non-genetic resistance to KRAS inhibitionNational Cancer Institute · 2025–2030
- Sub-PIR01CA289804-02The Genetic Epidemiology of Radiation-Associated Contralateral Breast CancerNational Cancer Institute · 2026–2030 · via Memorial Sloan Kettering Cancer Center
- MPIR01CA290616-02Defining the oncogenic potential and therapeutic dependencies of PDAC-associated KRAS variantsNational Cancer Institute · 2024–2029
- KPF31CA288132-01Understanding Kras Mutation Heterogeneity in PDACNational Cancer Institute · 2024–2027Fellowship
- PISRA 250524-01Agmen SRA : Understanding WNT dependence in CRCAmgen Inc. · 2025–2027Contract
- Sub-PIR01CA249678-04Biology of R-Spondin-Induced Sensitization to Asparaginase in Colorectal CancerNational Cancer Institute · 2021–2026 · via St. Jude Children's Research Hospital· 2 renewals
- PIHT9425-23-1-0728Defining the impact of Kras mutational heterogeneity on the tumor microenvironment in pancreatic cancerU.S. Department of Defense · 2023–2026
Completed grants (23)
- KPF31CA261061-01A1Interrogating the role of mutant KRAS allelic imbalance and co-mutated genes in targeted therapy response of NSCLCNational Cancer Institute · 2021–2025Fellowship
- Co-IR01CA234614-01A1Modeling Hepatoblastoma using pluripotent stem cell derived hepatocyte-like cellsNational Cancer Institute · 2019–2025
- PIR01CA229773-05In Vivo Base Editing for Precision Oncology ModelsNCI · 2019–2025 · via NIH RePORTER
- PI5 R01C A229773-05In Vivo Base Editing for Precision Oncology ModelsNational Cancer Institute · 2019–2025
- PISCC I16-0062Identifying acquired vulnerabilities driven by lineage plasticity and drug resistance in CRCStarr Cancer Consortium · 2023–2024
- KPR01CA270885-01Differential role of different NAD+ kinase Isoforms in melanoma metastasisNational Cancer Institute · 2022–2024
- KPK08CA241341-03Investigating the non-cell autonomous immune effects of mutant p53 in pancreatic cancerNational Cancer Institute · 2021–2024
- PIRMI 212909-01Revolution Medicines, Inc. BiopharmaRevolution Medicines, Inc. · 2020–2024BioPharma Alliance
- Co-ISU2C-AACR-DT22-17Targeting Genomic, Metabolic and Immunological Vulnerabilities of Colorectal CancerAmerican Association for Cancer Research · 2017–2024 · via Sloan-Kettering Institute for Cancer Research
- PIR01CA222517-05Progression, response, and resistance of RSPO fusion colorectal cancerNational Cancer Institute · 2018–2023
- PIBP 226002-01Defining the Genetic Determinants of Response to B-Catenin Blockade in CRCFog Pharmaceuticals, Inc. · 2022–2023BioPharma Alliance
- PISCC I14-0023Defining the cancer stem cell nicheStarr Cancer Consortium · 2021–2022
- KPF31CA247351-01Sensitizing Colorectal Cancer to Checkpoint Inhibitors by WNT Pathway SuppressionNational Cancer Institute · 2020–2022Fellowship
- PIRSG-17-202-01-TBGTumor Dormancy and Therapy Resistance in RSPO Fusion CRCAmerican Cancer Society · 2018–2021
- PISYN 194391-01OVERCOMING OBSTACLES IN BASE EDITING WITH SYTHETIC GUIDE RNAsSynthego · 2019–2021
- KPF31CA224800-02Targeting the WNT Pathway in Colorectal CancerNational Cancer Institute · 2017–2021Fellowship
- Co-IR01CA205418-03Targeting the Epithelial to Mesenchymal Transition-Related Chemoresistance in Breast CancerNational Cancer Institute · 2016–2021
- KPK99CA218686-02Propionate Metabolism as an Essential Metabolic Adaptation for Tumor ProgressionNational Cancer Institute · 2017–2020Career
- PICONCERN 194724-01Targeting cancer-specific vulnerabilities in the WNT pathwayConcern Foundation · 2018–2020
- PISCC 17070948-01Investigating Cancer-Associated Structural Genomic Rearrangements Using in vivo Genome EditingStarr Cancer Consortium · 2017–2018
- PIDFI 180426-01Selective TNKS2 inhibition as a Collateral Vulnerability in Colorectal CancerDaedalus Fund for Innovation (Weill Cornell) · 2017–2018
- Sub-PIR01CA195787-03A scalable platform for target validation in GEMM models of gastrointestinalmalignancies.National Cancer Institute · 2015–2018 · via Sloan-Kettering Institute for Cancer Research
- PIK22CA181280-03Defining the genetic requirements for maintenance of colorectal cancerNCI · 2014–2017 · via NIH RePORTER
Available technologies
News mentions
- New Strategy May Target Common Cancer Driver with Minimal Side EffectsNovember 2, 2026
Researchers have found a surprisingly common vulnerability in a broad variety of cancers and have begun designing drug compounds to exploit it, in a study led by investigators at Weill Cornell Medicine.
- Targeting Inflammation May Help Overcome Drug Resistance in Colon CancerMay 21, 2026
According to a new preclinical study by Weill Cornell Medicine and MD Anderson Cancer Center investigators, colorectal tumors often find multiple ways to survive treatment, including additional genetic mutations and activation of cellular pathways typically associated with inflammation and regeneration.
- New Gene Editing Tool Helps Zero in on Small Cancer-Linked MutationsAugust 10, 2023
A new, very precise gene-editing tool created by Weill Cornell Medicine investigators will enable scientists to study the impact of these specific genetic changes in preclinical models rather than being limited to more broadly targeted tactics, such as deleting the entire gene.
- Cancer Research Teams Awarded Grants from Starr Cancer ConsortiumFebruary 10, 2023
Five teams led by Weill Cornell Medicine scientists have been awarded funding from the Starr Cancer Consortium in its 16th annual grant competition.
- Postdoctoral Fellow Honored with 2021 Tri-Institutional Breakout AwardJune 7, 2021
Dr. Maria Paz Zafra, a postdoctoral associate in medicine at Weill Cornell Medicine, has won a 2021 Tri-Institutional Breakout Award for Junior Investigators.
Show 1 more mention
- Gene Editing Yields New Models for Studying Common Cancer MutationsAugust 12, 2020
A new set of laboratory models designed to study variations in one of the most commonly mutated genes in cancer has revealed that each variation has a different effect on the colon and pancreas, according to investigators at Weill Cornell Medicine. The models also provide a new platform for screening potential therapies.
Media highlights
- Weill Cornell Finds Cancer-Cell Vulnerability, But Experimental Drug Remains At Lab StageFingerLakes1.com · November 3, 2026
Mentoring
- AKAlyna KattiCell & Developmental Biology (PhD) · Class of 2022
- THTeng HanCell & Developmental Biology (PhD) · Class of 2020
- BDBianca DiazCell & Developmental Biology (PhD) · Class of 2025
- JZJill ZimmermanCell & Developmental Biology · Class of 2024
- KCKevan ChuCell & Developmental Biology (PhD)
- WSWhitney SissoCell & Developmental Biology (PhD)
- MPMarie ParsonsPostdoc mentee · 2021–2025
- SBSara BernardoPostdoc mentee · 2023–2026
- JKJangkyung KimCell & Developmental Biology (PhD)
- MKMax KopsCell & Developmental Biology (PhD)
- SBSher BahadurBiochemistry, Cell & Molecular Biology (PhD)
External relationships
Other
Revolution Medicines, Inc.