Ellen Langer, Ph.D. (she/her)
- Assistant Professor of Division of Oncological Sciences, School of Medicine
- Assistant Professor of Molecular and Medical Genetics, School of Medicine
- Member, CEDAR, OHSU Knight Cancer Institute, School of Medicine
Biography
Dr. Langer received her Ph.D. in Molecular Cell Biology from Washington University in St. Louis under the mentorship of Dr. Greg Longmore, and she completed postdoctoral training with Dr. Ken Murphy, Dr. Mario Capecchi, and Dr. Rosalie Sears. Throughout her career, Dr. Langer has sought to understand how physiologic processes that occur during development or in response to injury are corrupted to contribute to tumor development and progression. Her early research focused on the transcriptional regulators that control epithelial to mesenchymal transitions (EMT) in developmental systems including Xenopus neural crest development and embryonic stem cell differentiation. During her postdoc, Dr. Langer interrogated mechanisms of phenotypic plasticity in breast cancer cells to understand how extrinsic stressors such as low nutrients or therapeutic treatments mediate changes in tumor cell phenotypes. She also co-led an effort to develop manipulable, heterotypic, 3D bioprinted tumor models to support investigations of how tumor-stromal crosstalk affects tumor phenotype and response to treatment.
Dr. Langer’s research is focused on interrogating mechanisms of cellular plasticity in both neoplastic and non-neoplastic cells in order to understand how interactions between these populations impact tumor development and progression. Current work in her group utilizes 2-dimensional tissue culture, 3-dimensional bioprinted tissues, and mouse models in order to identify and target mechanisms of crosstalk between tumor cells and stromal cells in breast and pancreatic cancer.
Education and training
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Degrees
- B.S., 2001, University of Notre Dame
- Ph.D., 2007, Washington University in St. Louis
Memberships and associations:
- American Association of Cancer Research
Publications
Publications
Ongoing replication stress tolerance and clonal T cell responses distinguish liver and lung recurrence and outcomes in pancreatic cancer
Nature CancerMicelle-Formulated Juglone Effectively Targets Pancreatic Cancer and Remodels the Tumor Microenvironment
PharmaceuticsMYC Deregulation and PTEN Loss Model Tumor and Stromal Heterogeneity of Aggressive Triple-Negative Breast Cancer
Nature communicationsSulfopin is a covalent inhibitor of Pin1 that blocks Myc-driven tumors in vivo
Nature Chemical BiologyAltering MYC phosphorylation in the epidermis increases the stem cell population and contributes to the development, progression, and metastasis of squamous cell carcinoma
OncogenesisDeregulating MYC in a model of HER2+ breast cancer mimics human intertumoral heterogeneity
Journal of Clinical InvestigationPIN1 Provides Dynamic Control of MYC in Response to Extrinsic Signals
Frontiers in Cell and Developmental BiologyModeling differentiation-state transitions linked to therapeutic escape in triple-negative breast cancer
PLoS computational biologyModeling Tumor Phenotypes In Vitro with Three-Dimensional Bioprinting
Cell ReportsDifferentiation-state plasticity is a targetable resistance mechanism in basal-like breast cancer
Nature communicationsZEB1-repressed microRNAs inhibit autocrine signaling that promotes vascular mimicry of breast cancer cells
OncogeneThe tumor suppressor phosphatase PP2A-B56α regulates stemness and promotes the initiation of malignancies in a novel murine model
PloS oneThe impact of chromosomal translocation locus and fusion oncogene coding sequence in synovial sarcomagenesis
OncogeneTargeting c-MYC by antagonizing PP2A inhibitors in breast cancer
Proceedings of the National Academy of Sciences of the United States of AmericaDual actions of Meis1 inhibit erythroid progenitor development and sustain general hematopoietic cell proliferation
BloodSnail promotes the cell-autonomous generation of Flk1 + endothelial cells through the repression of the microRNA-200 family
Stem Cells and DevelopmentSnail and the microRNA-200 family act in opposition to regulate epithelial-to-mesenchymal transition and germ layer fate restriction in differentiating ESCs
Stem CellsAjuba LIM proteins are snail/slug corepressors required for neural crest development in Xenopus.
Developmental CellMesp1 coordinately regulates cardiovascular fate restriction and epithelial-mesenchymal transition in differentiating ESCs
Cell Stem CellThe LIM protein AJUBA recruits protein arginine methyltransferase 5 to mediate SNAIL-dependent transcriptional repression
Molecular and cellular biologyThe Ajuba LIM domain protein is a corepressor for SNAG domain-mediated repression and participates in nucleocytoplasmic shuttling
Cancer ResearchBcl-xL deamidation is a critical switch in the regulation of the response to DNA damage
Cell