• Office
  • PAHL 4828
  • 54731
  • Lab:
  • PAHL 4814

Samuel Workenhe

Assistant Professor   |   D.V.M., PhD

Profile

DVM, Addis Ababa University, Ethiopia

MSc, Marine Biotechnology, University of Tromso, Norway

PhD, Molecular Virology, University of Prince Edward Island, Canada

Postdoctoral Fellowship, Cancer Immunology&Immunotherapy, McMaster Immunology Research Center, Canada

Research Interests

Overview of Research Program

My lab's research aims to understand how cell intrinsic processes such as sensing of pathogens, stress and metabolic states shape homeostatic processes such as activation of the immune system. We use a variety of stimuli, including different classes of viruses, synthetic ligands and ligand-free genetic circuits in healthy and transformed cell lines established from evolutionarily divergent animal species. A common theme is to understand the crosstalk of distinct molecular processes that serve as an innate guard against invading pathogens and malignancies. We also study how these innate processes, such as the type I interferon system and programmed cell death, shape the development of adaptive immunity against viruses and cancer. We continue to translate the basic findings into therapeutics for cancer and viral diseases. 

Specific Projects

1. Decoding how viral associated ligands activate programmed cell death: Sensing of viral nucleic acids can activate a variety of antiviral responses, including programmed cell death. Our understanding of how nucleic acid sensing shapes programmed cell death is largely unknown. Our laboratory uses synthetic circuits and a variety of genetic tools to study how antiviral signaling activates programmed cell death. The findings of this study are crucial to understanding the biology of programmed cell death.

2. Pathophysiological outcomes of cell death: Programmed cell death is a highly regulated process with several immune-related organismal outcomes that can be pathogenic or therapeutic. We study in what circumstances can programmed cell death become pathogenic/therapeutic and what are the mediators of these immunological consequences. We utilize a variety of discovery tools such as Mass Spectrometry, Single Cell RNA Sequencing, and genome-scale CRISPR/Cas9 screening platforms to discover new immunobiology. The knowledge gained is required to develop novel immunotherapies for cancer and viral diseases.

3. Mechanisms of tumor detection by the immune system: The immune system is a powerful ally to eliminate malignant cells. Mechanisms by which immunotherapy refractory cancers, such as breast, pancreatic and brain tumors, evade anticancer immune responses remain largely unknown. We deploy a variety of immune-resistant tumor models and genetic tools to understand the biology of tumor-induced adaptive resistance mechanisms.

 

Graduate Students

Jordon Inkol, PhD Student

Michael Westerveld, MSc Student

Ali Younis, MBS Student- 1 Year course based Masters degree

Shayla Verburg, BioCanRx Summer Student and 4th year Biomedical Sciences thesis student

Rebecca Lelievre, Summer USRA and 4th year Cellular and Molecular Biology thesis student

Yi Lin Sun, 4th year Biomedical Sciences student and Volunteer  

Teaching

Mechanisms of Disease - Invited Lecture on Cancer Immuntherapy

Professional Experience & Honours

2014 - Recipient of the Faculty of Health Sciences Outstanding Postdoctoral Achievement Award, McMaster University

2015 - Oncolytic Virus Conference Travel Award

2012 - American Society of Virology Travel Award

2008 - Recipient of Dr. Douglas W. Ehresmann Award, UPEI, Canada

2004 - 2006 - NORAD Graduate Student Fellowship, University of Tromso, Norway

Links

https://scholar.google.ca/citations?user=u40Ay9kAAAAJ&hl=en

https://pubmed.ncbi.nlm.nih.gov/?term=Workenhe+ST&size=50

 

Selected Publications

Cytokines in oncolytic virotherapy. Pol JG, Workenhe ST, Konda P, Gujar S, Kroemer G.Cytokine Growth Factor Rev. 2020 Dec;56:4-27. doi: 10.1016/j.cytogfr.2020.10.007.

Tumor-intrinsic determinants of immunogenic cell death modalities. Workenhe ST, Pol J, Kroemer G.Oncoimmunology. 2021 Mar 2;10(1):1893466. doi: 10.1080/2162402X.2021.1893466.

TRIM26 Facilitates HSV-2 Infection by Downregulating Antiviral Responses through the IRF3 Pathway. Dhawan T, Zahoor MA, Heryani N, Workenhe ST, Nazli A, Kaushic C.Viruses. 2021 Jan 6;13(1):70. doi: 10.3390/v13010070.

Immune checkpoint blockade in triple negative breast cancer influenced by B cells through myeloid-derived suppressor cells. Vito A, Salem O, El-Sayes N, MacFawn IP, Portillo AL, Milne K, Harrington D, Ashkar AA, Wan Y, Workenhe ST, Nelson BH, Bruno TC, Mossman KL.Commun Biol. 2021 Jul 12;4(1):859. doi: 10.1038/s42003-021-02375-9.

De novo necroptosis creates an inflammatory environment mediating tumor susceptibility to immune checkpoint inhibitors. Workenhe ST, Nguyen A, Bakhshinyan D, Wei J, Hare DN, MacNeill KL, Wan Y, Oberst A, Bramson JL, Nasir JA, Vito A, El-Sayes N, Singh SK, McArthur AG, Mossman KL. Commun Biol. 2020 Nov 4;3(1):645.

 

 

 

Search PubMed for additional publications by Dr. Workenhe.