Sampath K. Loganathan

Academic title(s): 

Assistant professor, Department of Otolaryngology, Head and Neck Surgery.
Co-Director, Head and Neck Cancer Research Laboratory.
Junior Scientist, Cancer Research Program, RI-MUHC.
Associate Member, Goodman Cancer Research Institute,
Departments of Experimental Surgery and Experimental Medicine.

Sampath K. Loganathan
Contact Information
Email address: 
sampath.loganathan [at] mcgill.ca
Degree(s): 

Ph.D.

Location: 
RI-MUHC, Glen site
Division: 
Otolaryngology Cancer Research Program
Current research: 

Laboratory utilizes the in vivo CRISPR methodology in mouse models of HNSCC and investigate oncological mechanisms that drive the HNSCC with the ultimate goal of developing novel drug targets to treat this deadly cancer. In collaboration with other faculty members in Head and Neck Surgery department, Cancer Research Program, RI-MUHC and Goodman Cancer Research Centre, we focus on:

  1. Establishing HNSCC mouse models of novel tumor suppressors
  2. Investigating drug targets from GPCR superfamily using in vivo CRISPR screening in HNSCC mouse models and
  3. Utilizing patient-derived xenograft models to study drug targets and oncological mechanisms in HNSCC

Lab website: http://loganathan.lab.mcgill.ca

Language(s) spoken: 
English
Tamil
Biography: 

Dr. Sampath Loganathan received his Ph.D. from University of Alberta under the supervision of Dr. Joe Casey, Department of Biochemistry. In 2015, he joined the lab of Dr. Daniel Schramek as a Post-Doctoral Fellow at Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto. He studied Head and Neck Squamous Cell Carcinoma (HNSCC) using CRISPR based mouse models, ultra-sound guided lenti-viral injections, functional genomic tools and identified several novel tumor suppressors in HNSCC.

Selected publications: 
  1. Loganathan SK, Schleicher K, Malik AA, Quevedo R, Langille E, Teng K, Oh R, Rahtod B, Tsai R, Tehrani PS, Pugh TJ, Gingras AC & Schramek D (2020) Rare driver mutations in head and neck squamous cell carcinomas converge on NOTCH signaling. Science, 367(6483):1264-1269.
  2. Loganathan SK and Casey JR. Corneal Dystrophy-Causing SLC4A11 Mutants: Suitability for Folding-Correction Therapy. Hum Mutat. 2014 Sep;35(9):1082-91

PubMed Link: https://pubmed.ncbi.nlm.nih.gov/?term=loganathan+SK&sort=date

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