Grant: Operating Grant
University of British Columbia
$774,156.00
Identifying Cytoprotective Responses Triggered Following Initial Exposure to Targeted Therapy: Defining Improved Treatment Strategies for Patients with HER-2 Positive Breast Cancer.
FY 2009-10
Summary
This research program is focused on the development of drug combinations for use in patients with relapsed breast cancer. More specifically, a significant number of women suffer from advanced breast cancers that express HER-2, a protein that is associated with more aggressive metastatic breast cancer. Trastuzumab is a drug specifically designed to treat individuals with HER-2 positive disease. Unfortunately, many patients who initially respond, when first treated with trastuzumab, will relapse with a disease that will be resistant to this drug. Therefore, we need to develop new effective drugs for this group of patients. The goal of this research program is to gain new insights into the mechanisms contributing to the behavior of HER-2 positive cancers when initially exposed to different drugs and learn how to fight these mechanisms to make treatments more effective and avoid problems with drug resistance. Here, we propose two research approaches. The first one is focused on addressing a transient (reversible) adaptive response called autophagy, a cellular mechanism protecting the cancer cells from cell death while treated with anti-cancer drugs. The studies proposed here will determine whether improved treatment responses can be achieved when we combine drugs that inhibit this protective response. The second goal is designed to identify other protective responses in HER-2 positive breast cancer cells that occur when they are first exposed to selected drugs. Once these protective responses are understood, then, genes or products of these genes, will be identified as new targets for treatment. Drugs against these targets would be extremely valuable when used in a combination with the agents that first elicited the protective response of cancer cells.
Department
Program
Operating Grant
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
202218
Name
Bally Marcel B
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Progression & Therapeutics 2
Projecttitle
Identifying Cytoprotective Responses Triggered Following Initial Exposure to Targeted Therapy: Defining Improved Treatment Strategies for Patients with HER-2 Positive Breast Cancer.
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$774,156
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Autophagy; Breast Cancer; Cytoprotective Responses; Drug Combinations; Trastuzumab Resistance; Tumour Models
Abstract
This research program is focused on the development of drug combinations for use in patients with relapsed breast cancer. More specifically, a significant number of women suffer from advanced breast cancers that express HER-2, a protein that is associated with more aggressive metastatic breast cancer. Trastuzumab is a drug specifically designed to treat individuals with HER-2 positive disease. Unfortunately, many patients who initially respond, when first treated with trastuzumab, will relapse with a disease that will be resistant to this drug. Therefore, we need to develop new effective drugs for this group of patients. The goal of this research program is to gain new insights into the mechanisms contributing to the behavior of HER-2 positive cancers when initially exposed to different drugs and learn how to fight these mechanisms to make treatments more effective and avoid problems with drug resistance. Here, we propose two research approaches. The first one is focused on addressing a transient (reversible) adaptive response called autophagy, a cellular mechanism protecting the cancer cells from cell death while treated with anti-cancer drugs. The studies proposed here will determine whether improved treatment responses can be achieved when we combine drugs that inhibit this protective response. The second goal is designed to identify other protective responses in HER-2 positive breast cancer cells that occur when they are first exposed to selected drugs. Once these protective responses are understood, then, genes or products of these genes, will be identified as new targets for treatment. Drugs against these targets would be extremely valuable when used in a combination with the agents that first elicited the protective response of cancer cells.
Competitiondate
201003
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Bally, Marcel B
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $774,156~ $0~