Author

A. T. Le

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cancer Biology· 5

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Organism:mouse· 4 Research Focus:cancer & tumor microenvironment· 3 Assay:bulk RNA-seq· 2 Research Focus:drug response / drug discovery· 2 Research Focus:cell type annotation· 1 Assay:CRISPR screen· 1 Approach:genetic perturbation / CRISPR· 1

Frequent Co-Authors

L. E. Heasley· 4 shared R. A. Nemenoff· 4 shared T. K. Hinz· 4 shared A. Navarro· 3 shared E. K. Kleczko· 3 shared E. T. Clambey· 2 shared R. C. Doebele· 2 shared T. T. Nguyen· 2 shared

Activity by Year

2022-2023 · peak 4/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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4 shared papersCancer Biology

L. E. Heasley

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

A Rapid, Functional sgRNA Screening Method for Generating Murine RET and NTRK1 Fusion Oncogenes

L. E. Heasley, L. Schubert, A. T. Le, T. K. Hinz, A. Navarro, S. K. Nelson-Taylor, R. A. Nemenoff, R. C. Doebele

This paper describes a method to validate sgRNAs that generate RET and NTRK1 fusion oncogenes in murine models, demonstrating their efficacy in creating tumor models responsive to targeted therapies.

bioRxiv · Apr 6, 2023 · PreprintCancer Biology

Novel EGFR-Mutant Mouse Models of Lung Adenocarcinoma Reveal Adaptive Immunity Requirement for Durable Osimertinib Response

L. E. Heasley, E. K. Kleczko, A. T. Le, T. K. Hinz, T. T. Nguyen, A. Navarro, C.-J. Hu, E. T. Clambey, D. T. Merrick, M. Weiser-Evans, R. A. Nemenoff

bioRxiv · Oct 26, 2022Cancer Biology

Evaluation of KRASG12C Inhibitor Responses in Novel Murine KRASG12C Lung Cancer Cell Line Models

D. J. Sisler, T. K. Hinz, A. T. Le, E. K. Kleczko, R. A. Nemenoff, L. E. Heasley

This paper develops three novel murine KRASG12C-driven lung cancer cell lines to evaluate responses to KRASG12C inhibitors and identify combination strategies for improved therapeutic outcomes.

bioRxiv · Aug 19, 2022Cancer Biology

Loss of Spindly sensitizes EML4-ALK v3 lung cancer cells to HSP90 inhibitors

M. P. Licciardello, C. Zhang, A. T. Le, R. C. Doebele, P. A. Clarke, P. Workman

The paper shows that loss of Spindly increases sensitivity of EML4-ALK v3 NSCLC cells to HSP90 inhibitors, but not v1 cells.

bioRxiv · Jun 8, 2022 · PreprintCancer Biology

Adaptive immunity is required for durable responses to alectinib in murine models of EML4-ALK lung cancer

E. K. Kleczko, T. K. Hinz, T. T. Nguyen, N. J. Gurule, A. Navarro, A. T. Le, A. M. Johnson, J. Kwak, D. I. Polhac, E. T. Clambey, M. C. Weiser-Evans, T. Patil, E. L. Schenk, L. E. Heasley, R. A. Nemenoff

This paper shows that adaptive immunity enhances the durability of alectinib response in EML4-ALK lung cancer models, with CD8+ T cells playing a key role.

bioRxiv · Apr 14, 2022 · PreprintCancer Biology