Katherine Michaelis

  • Current Program Year: MS4
  • Graduate, Physiology and Pharmacology Graduate Program, School of Medicine

Biography

Katherine is a current MS4 in the OHSU MSTP whose long-term goal is to become a physician-scientist in the field of pediatric oncology. Her research prior to medical school included exploring the molecular underpinnings of pituitary tumorigenesis and elucidating the role of NF-kB signaling in bronchopulmonary dysplasia and acute respiratory distress syndrome. As a graduate student in the lab of Daniel L. Marks, she took an interest in the intersection of tumor response, immunology, and systemic physiology in the context of pancreatic cancer. During this time, she established a high fidelity mouse model of pancreatic cancer cachexia (Michaelis et al, JCSM 2017). Next, she employed mouse models to determine whether the immune- enhancing agent R848, an agonist of Toll-like receptor 7 (TLR7), could be delivered in a manner to overcome sickness responses and allow safe therapeutic use (Michaelis et al, BBI 2019). Finally, she applied the optimized R848 dosing strategy to the mouse model of PDAC and cancer-associated cachexia, which revealed beneficial effects on both tumor response and cachexia status (Michaelis et al, Nature Communications 2019). 

In addition to her future goal of exploring novel therapeutic modalities for pediatric malignancies, Katherine is passionate about childhood cancer survivorship issues including late effects of treatment, cardiovascular health, and cognition.

Dissertation Title: Toll-like Receptor 7 as a Therapeutic Target in Pancreatic Ductal Adenocarcinoma and Cancer-Associated Cachexia

Education and training

    • B.A., 2010, University of Colorado, Boulder
    • Ph.D., 2019, Oregon Health & Science University

Memberships and associations:

  • American Academy of Pediatrics
  • American Association for Cancer Research
  • American Physician Scientist Association
  • Association for Clinical and Translational Research
  • American Medical Association

Honors and awards

  • The John A. Resko Outstanding Doctoral Thesis Award, 2020
  • Nature Communications Editor’s Highlight in Therapeutics, 2019
  • TL1 OSLER Fellowship for Clinical and Translational Research, 2017-2019

Publications

Selected publications

  • Michaelis, K.A., Norgard, M.A., Zhu, X., Levasseur, P.R., Sivagnanam, S., Liudahl, S.M., Burfeind, K.G., Olson, B., Pelz, K.R., Angeles Ramos, D.M., Maurer, H.C., Olive, K.P., Coussens, L.M., Morgan, T.K., and Marks, D.L. The TLR7/8 agonist R848 remodels tumor and host responses to promote survival in pancreatic cancer. Nat Commun. 2019 Oct 15;10(1):4682. doi: 10.1038/s41467-019-12657-w. Erratum in: Nat Commun. 2019 Nov 15;10(1):5257. PMID: 31615993; PMCID: PMC6794326.
  • Michaelis, K.A., Norgard, M.A., Levasseur, P.R., Olson, B., Burfeind, K.G., Buenafe, A.C., Zhu, X., Jeng, S., McWeeney, S.K., and Marks, D.L. Persistent Toll-like receptor 7 stimulation induces behavioral and molecular innate immune tolerance. Brain Behav Immun. 2019 Sep 6. pii: S0889-1591(19)30525-2.
  • Zhu, X., Burfeind, K.G., Michaelis, K.A., Braun, T.P., Olson, B., Pelz, K.R., Morgan, T.K., and Marks, D.L. MyD88 signalling is critical in the development of pancreatic cancer cachexia. J Cachexia Sarcopenia Muscle. 2019 Apr;10(2):378-390.
  • Michaelis, K. A., Zhu, X., Burfeind, K. G., Krasnow, S. M., Levasseur, P. R., Morgan, T. K., & Marks, D. L. (2017). Establishment and characterization of a novel murine model of pancreatic cancer cachexia. Journal of cachexia, sarcopenia and muscle8(5), 824–838. https://doi.org/10.1002/jcsm.12225
  • Burfeind, K. G. #, Michaelis, K. A. #, & Marks, D. L. (2016). The central role of hypothalamic inflammation in the acute illness response and cachexia. Seminars in cell & developmental biology54, 42–52. https://doi.org/10.1016/j.semcdb.2015.10.038 (#, co-first authors)
  • McKenna, S., Michaelis, K. A., Agboke, F., Liu, T., Han, K., Yang, G., Dennery, P. A., & Wright, C. J. (2014). Sustained hyperoxia-induced NF-?B activation improves survival and preserves lung development in neonatal mice. American journal of physiology. Lung cellular and molecular physiology306(12), L1078–L1089. https://doi.org/10.1152/ajplung.00001.2014
  • Michaelis, K. A., Agboke, F., Liu, T., Han, K., Muthu, M., Galambos, C., Yang, G., Dennery, P. A., & Wright, C. J. (2014). I?B?-mediated NF-?B activation confers protection against hyperoxic lung injury. American journal of respiratory cell and molecular biology50(2), 429–438. https://doi.org/10.1165/rcmb.2013-0303OC
  • Tang, J. R., Michaelis, K. A., Nozik-Grayck, E., Seedorf, G. J., Hartman-Filson, M., Abman, S. H., & Wright, C. J. (2013). The NF-?B inhibitory proteins I?B? and I?B? mediate disparate responses to inflammation in fetal pulmonary endothelial cells. Journal of immunology (Baltimore, Md. : 1950)190(6), 2913–2923. https://doi.org/10.4049/jimmunol.1202670
  • Xu, M., Knox, A. J., Michaelis, K. A., Kiseljak-Vassiliades, K., Kleinschmidt-DeMasters, B. K., Lillehei, K. O., & Wierman, M. E. (2012). Reprimo (RPRM) is a novel tumor suppressor in pituitary tumors and regulates survival, proliferation, and tumorigenicity. Endocrinology153(7), 2963–2973. https://doi.org/10.1210/en.2011-2021
  • Michaelis, K. A., Knox, A. J., Xu, M., Kiseljak-Vassiliades, K., Edwards, M. G., Geraci, M., Kleinschmidt-DeMasters, B. K., Lillehei, K. O., & Wierman, M. E. (2011). Identification of growth arrest and DNA-damage-inducible gene beta (GADD45beta) as a novel tumor suppressor in pituitary gonadotrope tumors. Endocrinology152(10), 3603–3613. https://doi.org/10.1210/en.2011-0109

Publications

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