Grant: Master's Award: Canada Graduate Scholarships
Queen's University (Kingston, Ontario)
$17,500.00
Exploring Pro-Invasive Signalling Proteins in Colon Cancer
FY 2016-17
Summary
Within the human body, cells receive messages from their surroundings to control a variety of cellular functions, such as cell growth, survival, and movement. These messages are received by molecules on the cell surface (receptors) which convey the signals into the cell to alter cell activity. This signalling system is required for normal tissue development, however when this goes awry in cancer cells, the disease can grow and spread. We are interested in a cell surface receptor named RET, which can cause cancer cells to spread to other parts of the body. There are multiple ways cancer can spread, one of which is when cancer cells invade nearby nerves (perineural invasion). Perineural invasion is prevalent in colorectal cancers, where it causes pain and is associated with poor patient outcomes. Thus, our goals are to identify how RET and its signalling system contribute to colorectal cancer perineural invasion. We will do this by analyzing colorectal tumor samples for RET expression to see how RET levels correlate to tumor invasiveness. Additionally, we will model the process of perineural invasion by co-culturing neural cells with colorectal cancer cells. We will use this model to explore how RET signalling alters cancer cell motility and invasiveness in the neural environment. This will be done through a variety of visualization methods and molecular techniques we have previously developed to quantify cell invasion in a RET-dependent manner. Together, our experiments will further characterize the mechanisms of RET-mediated tumor spread. We ultimately hope to identify how RET and its signalling pathways may be potential candidates to target during colorectal cancer treatment.
Department
Program
Master's Award: Canada Graduate Scholarships
Location
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
367220
Name
Maritan Sarah M
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Prcname2
Special Cases - Awards Programs
Projecttitle
Exploring Pro-Invasive Signalling Proteins in Colon Cancer
Programtype2
Studentship Programs
Orgnameinp2
Queen's University (Kingston, Ontario)
Cihramount2
$17,500
Cihrequipment2
$0
Programname2
Master's Award: Canada Graduate Scholarships
Keyworddelim
Cancer; Cell Signalling; Colorectal; Invasion; Metastasis; Migration; Perineural; Receptor Tyrosine Kinase; Ret; Three Dimensional
Abstract
Within the human body, cells receive messages from their surroundings to control a variety of cellular functions, such as cell growth, survival, and movement. These messages are received by molecules on the cell surface (receptors) which convey the signals into the cell to alter cell activity. This signalling system is required for normal tissue development, however when this goes awry in cancer cells, the disease can grow and spread. We are interested in a cell surface receptor named RET, which can cause cancer cells to spread to other parts of the body. There are multiple ways cancer can spread, one of which is when cancer cells invade nearby nerves (perineural invasion). Perineural invasion is prevalent in colorectal cancers, where it causes pain and is associated with poor patient outcomes. Thus, our goals are to identify how RET and its signalling system contribute to colorectal cancer perineural invasion. We will do this by analyzing colorectal tumor samples for RET expression to see how RET levels correlate to tumor invasiveness. Additionally, we will model the process of perineural invasion by co-culturing neural cells with colorectal cancer cells. We will use this model to explore how RET signalling alters cancer cell motility and invasiveness in the neural environment. This will be done through a variety of visualization methods and molecular techniques we have previously developed to quantify cell invasion in a RET-dependent manner. Together, our experiments will further characterize the mechanisms of RET-mediated tumor spread. We ultimately hope to identify how RET and its signalling pathways may be potential candidates to target during colorectal cancer treatment.
Competitiondate
201612
Approvedterm2
1 yr 0 mth
Pinamesdelim
Maritan, Sarah M
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $17,500~ $0~