Dr. Daniel Durocher

PhD FRSC
Senior Investigator

Lunenfeld-Tanenbaum Research Institute

Genomic instability, DNA damage response and cancer therapeutics

The major objective of the work done in our laboratory is to understand the molecular processes by which cells preserve the stability of their entire DNA – their genome– and to use this knowledge to develop therapeutic strategies, particularly for cancer treatment. 

We investigate how cells sense, signal and repair DNA damage, and how defects in these pathways contribute to disease. To address these questions, we use a broad range of approaches, including genetic, biochemical, functional genomic and proteomic methods. We employ the gene editing tool, CRISPR, to systematically inactivate genes in cancer cells. This allows us to identify genes and molecular processes that are essential for the growth of cancer cells, but not healthy cells and which could therefore be targeted for therapy. 

Our research has provided insights into the DNA damage response processes and has revealed targets that can selectively kill cancer cells with specific DNA repair defects. A key goal for our team is to translate these findings into therapeutic approaches. We have engaged in multiple successful collaborations with industrial partners to accelerate this process, bridging fundamental research and translation. 

Telephone
Contact

Email: [email protected]

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Location

Room 1073, 600 University Avenue
Toronto, M5G 1X5

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Related links

Website: Durocher Lab
Publications: Pubmed

Accordion Items
  • 2021–present; Co-founder, Induxion Therapeutics
  • 2016–present; Co-founder, Repare Therapeutics
  • 2011–present; Professor, Department of Molecular Genetics, University of Toronto, Toronto
  • 2007–present; Senior Investigator, Lunenfeld-Tanenbaum Research Institute, Sinai Health, Toronto
  • BSc, Biochemistry, Université de Montréal, Montreal, Canada; 1990–1993
  • PhD, Experimental Medicine, McGill University, Montreal, Canada; 1993–1998
  • Postdoctoral fellowship, University of Cambridge, UK; 1997–2001 

Our group is near capacity but we are always encouraging motivated researchers to contact us.

Graduate students
Note that our research group is part of the Molecular Genetics department at the University of Toronto, which has a central admission committee and a rotation system. Graduate students interested in doing a PhD in the laboratory must first be accepted in the department. You can find more information here

Summer students 
Summer students are selected from successful applicants to the Research Training Center (RTC) at the Lunenfeld-Tanenbaum Research Institute. Applications are available online and need to be filled by February 28th of each year.  

Notable publications

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CCNE1 amplification is synthetic lethal with PKMYT1 kinase inhibition

Nature, 2022

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The CIP2A–TOPBP1 axis safeguards chromosome stability and is a synthetic lethal target for BRCA-mutated cancer

Nature Cancer, 2021

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A Genetic Map of the Response to DNA Damage in Human Cells

Cell, 2020

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The shieldin complex mediates 53BP1-dependent DNA repair

Nature, 2018

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CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesions

Nature, 2018

Join our team

Visit our job board to see research positions.