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Julie L. Kadrmas, PhD

Languages spoken: English

Academic Information

Departments: Oncological Sciences - Research Assistant Professor

Academic Office Information

(801) 587-4634

Huntsman Cancer Hospital
Department of Oncological Sciences
1950 Circle of Hope, Room: 5322
Salt Lake City, UT 84112

Research Interests

  • Integrin Signaling
  • Integrin Adhesion
  • Cell Migration
  • Metastasis
Julie Kadrmas, Ph.D. is an investigator in the Cell Response and Regulation Program at the Huntsman Cancer Institute. Her group is interested in understanding regulatory mechanisms controlling cell adhesion and migration, with implications for how cancer cells gain the capacity to leave the site of a primary tumor and migrate during metastasis. Through the examination of normal developmental processes in the fruit fly Drosophila melanogaster, they characterize the functions of the integrin family of transmembrane receptors in regulating cell attachment and movement. Of particular interest is a molecular scaffolding protein called PINCH, which physically associates with integrins, as well as several additional PINCH protein partners that impinge upon distinct signaling cascades. Their work will provide a molecular understanding of how protein-protein interactions mediated by molecular scaffolds such as PINCH, integrate signals between multiple pathways to coordinate complex biological processes like cell adhesion and migration.

Education History

Postdoctoral Fellowship University of Utah, Department of Chemistry
Postdoctoral Fellow
Fellowship Duke University, National Institutes of Health
Doctoral Training Duke University
Undergraduate Bowling Green State University
Biology & Chemistry

Selected Publications

  1. Kadrmas JL, Beckerle MC, Yoshigi M (2020). Genetic analyses in mouse fibroblast and melanoma cells demonstrate novel roles for PDGF-AB ligand and PDGF receptor alpha. Sci Rep, 10(1), 19303.
  2. Wang Y, Antunes M, Anderson AE, Kadrmas JL, Jacinto A, Galko MJ (2015). Integrin Adhesions Suppress Syncytium Formation in the Drosophila Larval Epidermis. Curr Biol, 25(17), 2215-27.
  3. Ojelade SA, Jia T, Rodan AR, Chenyang T, Kadrmas JL, Cattrell A, Ruggeri B, Charoen P, Lemaitre H, Banaschewski T, Buchel C, Bokde AL, Carvalho F, Conrod PJ, Flor H, Frouin V, Gallinat J, Garavan H, Gowland PA, Heinz A, Ittermann B, Lathrop M, Lubbe S, Martinot JL, Paus T, Smolka MN, Spanagel R, OReilly PF, Laitinen J, Veijola JM, Feng J, Desrivieres S, Jarvelin MR, Schumann G, Rothenfluh A (2015). Rsu1 regulates ethanol consumption in Drosophila and humans. Proc Natl Acad Sci U S A, 112(30), E4085-93.
  4. Clark KA, Kadrmas JL (2013). Drosophila melanogaster muscle LIM protein and alpha-actinin function together to stabilize muscle cytoarchitecture: a potential role for Mlp84B in actin-crosslinking. Cytoskeleton (Hoboken), 70(6), 304-16.
  5. Yoshigi M, Pronovost SM, Kadrmas JL (2013). Interactions by 2D Gel Electrophoresis Overlap (iGEO): a novel high fidelity approach to identify constituents of protein complexes. Proteome Sci, 11(1), 21.
  6. Pronovost SM, Beckerle MC, Kadrmas JL (2013). Elevated expression of the integrin-associated protein PINCH suppresses the defects of Drosophila melanogaster muscle hypercontraction mutants. PLoS Genet, 9(3), e1003406.
  7. Elias MC, Pronovost SM, Cahill KJ, Beckerle MC and Kadrmas JL (2012). A crucial role for Ras suppressor-1 (RSU-1) revealed when PINCH and ILK binding is disrupted. J Cell Sci, 125, 3185-3194.
  8. Kadrmas JL, Smith MA, Pronovost SM, Beckerle MC (2007). Characterization of RACK1 function in Drosophila development. Dev Dyn, 236(8), 2207-15.
  9. Kadrmas JL, Smith MA, Clark KA, Pronovost SM, Muster N, Yates JR 3rd, Beckerle MC (2004). The integrin effector PINCH regulates JNK activity and epithelial migration in concert with Ras suppressor 1. J Cell Biol, 167(6), 1019-24.
  10. Kadrmas JL, Beckerle MC (2004). The LIM domain: from the cytoskeleton to the nucleus. [Review]. Nat Rev Mol Cell Biol, 5(11), 920-31.