Dr Thomas Pulliam

Grant-Funded Researcher (B)

SAIGENCI

College of Health


Dr Thomas Pulliam is a postdoctoral research fellow in the lab of Professor Lisa Butler where he undertakes prostate cancer research including treatment response prediction, testing the efficacy of novel drugs, spatial multiomics, nutrition/diet studies, and lipid metabolism.  
 
Dr Pulliam recieved his PhD in Cell and Molecular Biology from the Univeristy of Houston in 2021. He conducted his postdoctoral training at MD Anderson Cancer Center in Houston, Texas where he studied the interaction of androgen receptor (AR) signaling, metabolism, and angiogensis in advanced stage prostate cancer. He also aided in the development of novel inhibitors of Calcium/calmodulin-dependent protein kinase kinase 2 (CAMKK2), an AR regulated gene shown to drive prostate cancer progression through metabolic adaptation. 

Date Position Institution name
2026 - ongoing Postdoctoral Fellow University of Adelaide
2021 - 2026 Postdoctoral Fellow The University of Texas MD Anderson Cancer Center
2017 - 2021 Graduate Research Assistant University of Houston
2015 - 2017 Graduate Teaching Assistant University of Houston
2014 - 2014 Beach Water Sample Analyzer Texas General Land Office
2008 - 2012 Chemical, Biological, Radiological, Nuclear Defense Specialist United States Marine Corps

Date Institution name Country Title
2015 - 2021 University of Houston United States PhD
2012 - 2014 Lamar University United States Bachelors

Date Title Institution Country
2026 Postdoctoral Fellow University of Adelaide Australia
2021 - 2026 Postdoctoral Fellow The University of Texas MD Anderson Cancer Center United States

Year Citation
2025 Lin, C., Pulliam, T. L., Han, J. J., Xu, J., Recio, C. V., Wilkenfeld, S. R., . . . Frigo, D. E. (2025). Cholesterol metabolism regulated by CAMKK2-CREB signaling promotes castration-resistant prostate cancer. Cell Reports, 44(6), 115792.
DOI
2024 Awad, D., Cao, P. H. A., Pulliam, T. L., Spradlin, M., Subramani, E., Tellman, T. V., . . . Frigo, D. E. (2024). Adipose Triglyceride Lipase Is a Therapeutic Target in Advanced Prostate Cancer That Promotes Metabolic Plasticity.. Cancer research, 84(5), 703-724.
DOI Europe PMC20
2022 Pulliam, T. L., Goli, P., Awad, D., Lin, C., Wilkenfeld, S. R., & Frigo, D. E. (2022). Regulation and role of CAMKK2 in prostate cancer.. Nature reviews. Urology, 19(6), 367-380.
DOI Europe PMC30
2022 Pulliam, T. L., Awad, D., Han, J. J., Murray, M. M., Ackroyd, J. J., Goli, P., . . . Frigo, D. E. (2022). Systemic Ablation of <i>Camkk2</i> Impairs Metastatic Colonization and Improves Insulin Sensitivity in TRAMP Mice: Evidence for Cancer Cell-Extrinsic CAMKK2 Functions in Prostate Cancer.. Cells, 11(12), 1890.
DOI Europe PMC11
2021 Lin, C., Blessing, A. M., Pulliam, T. L., Shi, Y., Wilkenfeld, S. R., Han, J. J., . . . Frigo, D. E. (2021). Inhibition of CAMKK2 impairs autophagy and castration-resistant prostate cancer via suppression of AMPK-ULK1 signaling.. Oncogene, 40(9), 1690-1705.
DOI Europe PMC51
2021 Eduful, B. J., O'Byrne, S. N., Temme, L., Asquith, C. R. M., Liang, Y., Picado, A., . . . Drewry, D. H. (2021). Hinge Binder Scaffold Hopping Identifies Potent Calcium/Calmodulin-Dependent Protein Kinase Kinase 2 (CAMKK2) Inhibitor Chemotypes.. Journal of medicinal chemistry, 64(15), 10849-10877.
DOI Europe PMC23
2018 Awad, D., Pulliam, T. L., Lin, C., Wilkenfeld, S. R., & Frigo, D. E. (2018). Delineation of the androgen-regulated signaling pathways in prostate cancer facilitates the development of novel therapeutic approaches.. Current opinion in pharmacology, 41, 1-11.
DOI Europe PMC9
2018 White, M. A., Tsouko, E., Lin, C., Rajapakshe, K., Spencer, J. M., Wilkenfeld, S. R., . . . Frigo, D. E. (2018). GLUT12 promotes prostate cancer cell growth and is regulated by androgens and CaMKK2 signaling.. Endocrine-related cancer, 25(4), 453-469.
DOI Europe PMC51

Year Citation
2019 Lin, C., Salzillo, T. C., Bader, D. A., Wilkenfeld, S. R., Awad, D., Pulliam, T. L., . . . Frigo, D. E. (2019). Prostate Cancer Energetics and Biosynthesis.. In Advances in Experimental Medicine and Biology (Vol. 1210, pp. 185-237). Springer International Publishing.
DOI Europe PMC27

Year Citation
2022 Awad, D., Pulliam, T., Spradlin, M., Cao, P. H. -A., Subramani, E., Tellman, T., . . . Frigo, D. (2022). Adipose triglyceride lipase is regulated by CAMKK2-AMPK signaling and drives advanced prostate cancer.
DOI
2022 Wells, C., Liang, Y., Pulliam, T., Lin, C., Awad, D., Eduful, B., . . . Drewry, D. (2022). SGC-CAMKK2-1: A chemical probe for CAMKK2.
DOI
2020 Lin, C., Blessing, A., Pulliam, T., Shi, Y., Wilkenfeld, S., Han, J., . . . Frigo, D. (2020). Inhibition of CAMKK2 impairs autophagy and castration-resistant prostate cancer via suppression of AMPK-ULK1 signaling.
DOI

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