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Grant: Operating Grant - PA: Alberta Cancer Foundation - Research (bridge funding)

University of Alberta

$0.00

Role of lipid mediators in controlling migration and chemo-resistance in breast cancer cells

FY 2011-12

Summary
Treatment of breast and other cancers by a combination of surgery and chemotherapy is often unsuccessful and patients die. This is explained in two ways. Some tumor cells survive the surgery or they may have already spread to other areas of the body. Secondly, these cells fail to be killed by chemotherapy. Treatment with chemotherapeutic agents often becomes ineffective because of the progressive development of resistance to the effective use of these agents. The survival and spread (metastasis) of breast tumours to other organs is promoted by growth factors such as estrogens and epidermal growth factor. Several treatments of breast cancer depend on blocking these effects. Our project concentrates on a newly discovered growth factor called lysophosphatidate, which also plays an important role in promoting breast cancer. We showed that lysophosphatidate causes breast cancer cells to migrate to other organs and to resist being killed by several agents that are commonly used to treat breast cancer. So far, relatively little is know about lysophosphatidate with respect to the progression of breast cancer. Our proposed work will concentrate on discovering the mechanisms used by lysophosphatidate to promote the growth of breast tumours, their metastasis and the development of resistance to chemotherapy. This knowledge will be used to identify new therapeutic targets that can be used to block these adverse effects of lysophosphatidate. These developments should lead to the introduction of companion therapies that can be used to increase their effectiveness of existing treatments and to overcome the development of chemo-resistance. Overall, this should enhance our ability to increase the quality of life for breast cancer patients and maximize the chance of survival.
Program
Operating Grant - PA: Alberta Cancer Foundation - Research (bridge funding)
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
248570
Name
Brindley David N
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Alberta Cancer Foundation
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Molecular & Cellular Biology of Cancer
Projecttitle
Role of lipid mediators in controlling migration and chemo-resistance in breast cancer cells
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$0
Cihrequipment2
$0
Programname2
Operating Grant - PA: Alberta Cancer Foundation - Research (bridge funding)
Keyworddelim
Autotaxin; Chemo-Resistance; Doxorubicin; Lysophosphatidate; Phospholipase D; Sphingosine 1-Phosphate; Sphingosine Kinase; Taxol
Abstract
Treatment of breast and other cancers by a combination of surgery and chemotherapy is often unsuccessful and patients die. This is explained in two ways. Some tumor cells survive the surgery or they may have already spread to other areas of the body. Secondly, these cells fail to be killed by chemotherapy. Treatment with chemotherapeutic agents often becomes ineffective because of the progressive development of resistance to the effective use of these agents. The survival and spread (metastasis) of breast tumours to other organs is promoted by growth factors such as estrogens and epidermal growth factor. Several treatments of breast cancer depend on blocking these effects. Our project concentrates on a newly discovered growth factor called lysophosphatidate, which also plays an important role in promoting breast cancer. We showed that lysophosphatidate causes breast cancer cells to migrate to other organs and to resist being killed by several agents that are commonly used to treat breast cancer. So far, relatively little is know about lysophosphatidate with respect to the progression of breast cancer. Our proposed work will concentrate on discovering the mechanisms used by lysophosphatidate to promote the growth of breast tumours, their metastasis and the development of resistance to chemotherapy. This knowledge will be used to identify new therapeutic targets that can be used to block these adverse effects of lysophosphatidate. These developments should lead to the introduction of companion therapies that can be used to increase their effectiveness of existing treatments and to overcome the development of chemo-resistance. Overall, this should enhance our ability to increase the quality of life for breast cancer patients and maximize the chance of survival.
Competitiondate
201109
Approvedterm2
1 yr 0 mth
Pinamesdelim
Brindley, David N
Approvedterm
1 an 0 mois
University of Alberta - $0 Grant (2011-12) | Canada Spends