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Our primary research interests are focused around head and neck malignancies. These are a group of biologically similar tumors originating from tissue of the upper aerodigestive tract, including the lip, oral cavity (mouth), nasal passages, paranasal sinuses, oropharynx, and larynx. More than 4,300 Canadians will be diagnosed with this type of cancer this year and approximately 1,600 of them will die from it.
Currently, histopathological criteria are the gold standard for grading and classifying many tumor types. In recent years it has become clear that cancers with very similar morphologies may have drastically different underlying gene changes. Given that cancer is a disease driven by accumulated gene changes, it is imperative that we determine which of these changes are associated with specific clinical parameters. This will ultimately give us insight into mechanisms driving observed clinical behaviors (chemoresistance, metastasis, etc.) and provide us with effective biomarkers for guiding treatment strategies.
At the Garnis Lab, we are using molecular profiles of head and neck malignancies to better understand the gene changes involved in initiation and progression of this disease. We are looking into dysregulation of the genome and transcriptome (including non-coding RNAs) to develop molecular stratifications for what is presently treated as a homogeneous disease.
In addition to analyzing tumor tissues, we are investigating the utility of surface epithelial markers and blood-based biomarkers for managing disease. Surface epithelial markers may arise due to malignancy-associated changes (MACs) in normal tissues and may be useful for detecting disease when tumors arise in inaccessible locations, such as tonsillar crypts, which is common in the oropharynx. Regarding blood-based biomarkers, we are presently examining the oncogenic impacts of microRNAs that are secreted via extracellular vesicles (such as exosomes). These factors may not only have utility as biomarkers for early detection or disease recurrence; they may also be exploitable as therapeutic targets.
Currently, histopathological criteria are the gold standard for grading and classifying many tumor types. In recent years it has become clear that cancers with very similar morphologies may have drastically different underlying gene changes. Given that cancer is a disease driven by accumulated gene changes, it is imperative that we determine which of these changes are associated with specific clinical parameters. This will ultimately give us insight into mechanisms driving observed clinical behaviors (chemoresistance, metastasis, etc.) and provide us with effective biomarkers for guiding treatment strategies.
At the Garnis Lab, we are using molecular profiles of head and neck malignancies to better understand the gene changes involved in initiation and progression of this disease. We are looking into dysregulation of the genome and transcriptome (including non-coding RNAs) to develop molecular stratifications for what is presently treated as a homogeneous disease.
In addition to analyzing tumor tissues, we are investigating the utility of surface epithelial markers and blood-based biomarkers for managing disease. Surface epithelial markers may arise due to malignancy-associated changes (MACs) in normal tissues and may be useful for detecting disease when tumors arise in inaccessible locations, such as tonsillar crypts, which is common in the oropharynx. Regarding blood-based biomarkers, we are presently examining the oncogenic impacts of microRNAs that are secreted via extracellular vesicles (such as exosomes). These factors may not only have utility as biomarkers for early detection or disease recurrence; they may also be exploitable as therapeutic targets.
Research Interests
Papers共 110 篇Author StatisticsCo-AuthorSimilar Experts
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International journal of molecular sciencesno. 3 (2025)
Khanh Linh Tran,Sena Turkdogan, Anat Bahat Dinur,Thomas D. Milner,Edward Wang,Anthony Nichols,Danielle MacNeil,Adrian Mendez, Jake Jervis-Bardy,John De Almeida,Christopher Yao,David Goldstein,Ralph Gilbert,Antoine Eskander,Kevin Higgins,Danny Enepekides,Michael Gupta,Han Zhang,Michael Au,Sally Nguyen,Sidney Fels,Antony Hodgson, Penelope Brasher,Craig Mitton,Farahna Sabiq, Charles Fisher,David Yang, Angela Wong,Cathie Garnis,Catherine Poh,J. Scott Durham,Eitan Prisman
BMC Cancerno. 1 (2025): 1-10
International Journal of Molecular Sciencesno. 2 (2024): 1300-1300
Peter Y. F. Zeng,Stephenie D. Prokopec,Stephen Y. Lai,Nicole Pinto,Michelle A. Chan-Seng-Yue,Roderick Clifton-Bligh,Michelle D. Williams,Christopher J. Howlett,Paul Plantinga,Matthew J. Cecchini,Alfred K. Lam,Iram Siddiqui, Jianxin Wang,Ren X. Sun,John D. Watson,Reju Korah,Tobias Carling,Nishant Agrawal,Nicole Cipriani,Douglas Ball,Barry Nelkin,Lisa M. Rooper,Justin A. Bishop,Cathie Garnis, Ken Berean,Norman G. Nicolson,Paul Weinberger,Ying C. Henderson,Christopher M. Lalansingh,Mao Tian,Takafumi N. Yamaguchi,Julie Livingstone,Adriana Salcedo,Krupal Patel,Frederick Vizeacoumar,Alessandro Datti,Liu Xi,Yuri E. Nikiforov,Robert Smallridge,John A. Copland,Laura A. Marlow,Martin D. Hyrcza,Leigh Delbridge,Stan Sidhu,Mark Sywak,Bruce Robinson,Kevin Fung,Farhad Ghasemi,Keith Kwan,S. Danielle MacNeil,Adrian Mendez,David A. Palma,Mohammed I. Khan,Mushfiq Shaikh,Kara M. Ruicci,Bret Wehrli,Eric Winquist,John Yoo,Joe S. Mymryk,James W. Rocco,David Wheeler,Steve Scherer,Thomas J. Giordano,John W. Barrett,William C. Faquin,Anthony J. Gill,Gary Clayman,Paul C. Boutros,Anthony C. Nichols
Cell reportsno. 3 (2024): 113826-113826
Jessica Angelina Trejo Vazquez,Rebecca Towle, Dylan Andrew Farnsworth, Masih Sarafan, William Wallace Lockwood,Cathie Garnis
BIOMEDICINESno. 11 (2024)
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2023)
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#Papers: 110
#Citation: 2810
H-Index: 28
G-Index: 52
Sociability: 6
Diversity: 3
Activity: 13
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