Faculty Members Currently Qualified to Supervise Graduate Students
Dr. Kristi Baker |
Our lab studies differences in how the specialized mucosal immune in the intestine sees tumors with different patterns of genomic instability and how this translates into different forms of anti-tumor immune responses.
More... |
Dr. Vickie Baracos |
Metabolism in
wasting disorders: skeletal muscle atrophy and
cancer-associated cachexia. A number of pathological
states may be defined as wasting disorders - several
examples include cancer, AIDS, chronic obstructive
pulmonary disease. My research program focuses on the
metabolic abnormalities that underlie this wasting,
particularly of the skeletal muscles.
More... |
Dr. Gordon Chan |
In my laboratory, research is centered on the mechanism
of cell cycle control and particularly the regulation of
accurate, chromosome segregation during mitosis. The
mitotic checkpoint is a failsafe mechanism by which the
cell prevents premature anaphase and ensures accurate
chromosome segregation. By investigating the
molecular mechanism of the mitotic checkpoint, we can
better evaluate these genes as potential cancer drug
targets as well as contributing to the basic
understanding of cancer.More |
Dr. Yangxin Fu |
The objective of the Fu laboratory is to better understand the molecular mechanisms underlying ovarian tumorigenesis, with a particular interest in the role of Notch signaling pathway in ovarian cancer development and progression. More...
|
Dr. Armin Gamper |
My research examines how cells respond to genotoxic stress, how aberrant regulation of these response pathways affects tumorigenesis and how the DNA damage response can be targeted by drugs to improve radiation or chemotherapy. By studying the influence of genetic factors on the DNA damage response, I hope to discover diagnostic and predictive biomarkers that can be applied for personalized medicine. My approach integrates protein chemistry, proteomics, reverse chemical genetics, molecular and cell biological methods, and animal models.
More...
|
Dr. Roseline Godbout |
Retinoblastoma, a childhood tumour of the retina,
results from malignant transformation of precursor
cells. Retinal precursors are multipotent
neuroectodermal cells that can differentiate into all
the different types of neuronal and glial cells that
make up the mature tissue. There are currently two major projects in the lab. The first is to study the function and regulation of genes that are expressed at the early stages of retinal development. The second is to study the role of the DEAD box gene DDX1, encoding an RNA unwinding protein, in normal retinal development and in retinoblastoma. More... |
Dr. Michael Hendzel |
In my laboratory, we are examining how chromatin and
regulatory molecules are compartmentalized within the
cell nucleus. Our current research programs involve
defining the dynamics of movement of chromatin,
subnuclear structures involved in compartmentalizing
regulatory molecules that act on chromatin and RNA, and
the movement of individual regulatory molecules within
the cell nucleus. We have found that most molecules move
considerably slower than expected for their molecular
weight. More... |
Dr. Ismail Ismail |
More... |
Dr. Mary Hitt |
My research focuses on the development of gene therapy
vectors that minimize these side effects without
compromising anticancer activity. Currently we are
investigating adenovirus vectors carrying modified fiber
proteins and/or tissue-specific promoters to target
expression of toxic genes specifically to the tumor.
More... |
Dr. John Lewis
|
We study prostate cancer, the most commonly diagnosed cancer in Canadian men. Our goal is to foster an environment where scientists, doctors and clinical researchers work together to address key challenges in prostate cancer care. As a team, we hope to accelerate the transfer of research discoveries from the "bench to the bedside" to make an impact on those living with cancer. More... |
Dr. David Murray |
The basic research in my
laboratory focuses on understanding the basic
mechanisms by which mammalian cells respond to ionizing
radiation and
DNA-damaging anticancer drugs, with an emphasis on
DNA-repair pathways. My major
area of translational research interest is in
identifying the genetic factors
(polymorphisms) that determine the extreme response of
some cancer patients to
anticancer therapeutics such as radiation therapy and
cisplatin-based
chemotherapy.
More...
|
Dr. Lynne-Marie Postovit |
One of our major goals is to see the work that we do in the lab translate into new treatments or early detection methods for cancer patients: We want to translate our scientific results into clinical practice.
More.... |
Dr.Alan Underhill |
The Underhill laboratory is interested in
deciphering how master regulators of melanocyte development contribute to
melanoma pathogenesis. In addition, we are also examining how histone
modifications regulate the balance between cell proliferation and
differentiation, and how this is overridden in cancer..
More....
|
Dr. Michael Weinfeld |
Several years ago we
developed a postlabelling assay that allowed us to
detect a number of lesions in irradiated DNA. We have
applied this assay to the study of drugs that enhance
the level of DNA damage in radioresistant and
chemotherapy-resistant hypoxic cells. We observed that
these drugs can mimic oxygen by producing DNA strand
breaks with specific termini that require additional
processing before the strands can be rejoined. We have
also made use of the assay to monitor the repair of
these lesions by purified enzymes and cell-free
extracts.
More.... |
Dr. Frank Wuest |
My research is embedded in the multidisciplinary field of translational cancer research. Research efforts are mainly aimed at the evaluation and translation of the diagnostic and therapeutic potential of novel molecular targets involved in the development and progression of cancer by means of molecular imaging techniques to enhance patient care.
More.... |