Grant: Doctoral: Vanier Canada Graduate Scholarships
Queen's University (Kingston, Ontario)
$150,000.00
Identification of Novel Receptors Tyrosine Kinases (RTKs) Regulating the Hippo Signaling Pathway in Tumorigenesis
EF 2016-17
Résumé
Lung cancer kills 1.6 million people each year worldwide and is the most fatal cancer for Canadian men and women. Despite major progress in our understanding of the causes of lung cancer, more than 85% of lung cancer patients still die within 5 years after diagnosis. The poor prognosis associated with lung cancer is in part due to lack of effective drugs and "druggable" targets, or can be due to the development of resistance to drugs after initial treatment. Therefore, there is an urgent need to determine what cellular changes cause lung cancer to spread and develop drug resistance, and to identify new druggable targets. Our research group and others have recently discovered that changes in the Hippo signalling pathway are critical for the development and spread of lung cancers and also for their resistance to therapeutic drugs. However, the precise ways in which Hippo promotes cancer growth and metastasis is not completely known and there are currently no drugs available that can directly target Hippo for lung cancer therapy. For this project, I have developed a light emission-based biosensor tool, to detect interactions between un-known proteins involved in Hippo signalling. This powerful tool allows us to discover novel regulators of the Hippo pathway, which are capable of promoting cancer cell proliferation and metastasis in cancer cells. We are the first group in the world who have used this approach to find novel regulators of cell proliferation in lung cancer. Results from this study will identify new cellular pathways that interact with the Hippo pathway, thereby contributing significantly to the Hippo pathway research field and will have the potential to provide us with novel targets for cancer therapy. In the future, I will use different strategies to further determine the connection between these candidates and cancer, thus providing a new therapeutic strategy for successful cancer treatment.
Programme
Doctoral: Vanier Canada Graduate Scholarships
Bénéficiaire
Emplacement
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
362788
Name
Azad Taha
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Vanier Canada Graduate Scholarships CIHR
Projecttitle
Identification of Novel Receptors Tyrosine Kinases (RTKs) Regulating the Hippo Signaling Pathway in Tumorigenesis
Programtype2
Studentship Programs
Orgnameinp2
Queen's University (Kingston, Ontario)
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
Doctoral: Vanier Canada Graduate Scholarships
Keyworddelim
Breast Cancer; Cancer Biology; Lung Cancer; Metastasis; Split Luciferase Complementation Assay
Abstract
Lung cancer kills 1.6 million people each year worldwide and is the most fatal cancer for Canadian men and women. Despite major progress in our understanding of the causes of lung cancer, more than 85% of lung cancer patients still die within 5 years after diagnosis. The poor prognosis associated with lung cancer is in part due to lack of effective drugs and "druggable" targets, or can be due to the development of resistance to drugs after initial treatment. Therefore, there is an urgent need to determine what cellular changes cause lung cancer to spread and develop drug resistance, and to identify new druggable targets. Our research group and others have recently discovered that changes in the Hippo signalling pathway are critical for the development and spread of lung cancers and also for their resistance to therapeutic drugs. However, the precise ways in which Hippo promotes cancer growth and metastasis is not completely known and there are currently no drugs available that can directly target Hippo for lung cancer therapy. For this project, I have developed a light emission-based biosensor tool, to detect interactions between un-known proteins involved in Hippo signalling. This powerful tool allows us to discover novel regulators of the Hippo pathway, which are capable of promoting cancer cell proliferation and metastasis in cancer cells. We are the first group in the world who have used this approach to find novel regulators of cell proliferation in lung cancer. Results from this study will identify new cellular pathways that interact with the Hippo pathway, thereby contributing significantly to the Hippo pathway research field and will have the potential to provide us with novel targets for cancer therapy. In the future, I will use different strategies to further determine the connection between these candidates and cancer, thus providing a new therapeutic strategy for successful cancer treatment.
Competitiondate
201611
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Azad, Taha
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~