Grant: Operating Grant - Priority Announcement: Breast Cancer
University of British Columbia
$100,000.00
The endoplasmic reticulum-mitochondria interface and its regulation by the Gp78 ubiquitin ligase
FY 2014-15
Summary
Select breast cancers and certain other cancers are more difficult to treat, resulting in devastating diagnoses. Autocrine motility factor (AMF) and its receptor, Gp78, promote tumor cell motility and metastasis and are linked to malignancy in various cancers. Gp78 is found both at the cell surface, where it internalizes AMF from outside the cell, and also inside the cell in the endoplasmic reticulum, where it targets proteins for degradation. Gp78 is found in regions of the endoplasmic reticulum that interact with mitochondria, the energy producing organelle of the cell, where it breaks down mitochondrial proteins and controls the movement and destruction of mitochondria. Both the endoplasmic reticulum and mitochondria play important roles in cell death. We hypothesize that AMF and Gp78 act at the level of these cellular components to promote the survival of tumor cells leading to tumor progression and malignancy.
We will now study how AMF controls Gp78 function in breast cancer and whether AMF control of Gp78 in the endoplasmic reticulum affects its ability to promote tumor malignancy. We made an experimental mouse that expresses elevated levels of Gp78 in breast tissue. We will now generate a mouse that overexpresses AMF in breast tissue and also study mice that lack Gp78. These studies will allow us to determine the relationship between AMF interaction with Gp78 and breast cancer development. We are optimistic that our knowledge translation approach to share research results will enable new mechanistic understandings that will lead to new diagnostic and therapeutic approaches to better treat these potentially terminal cancers and provide a more hopeful prognosis for these cancer patients.
Department
Program
Operating Grant - Priority Announcement: Breast Cancer
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
328750
Name
Nabi Ivan R
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cell Biology & Mechanisms of Disease
Projecttitle
The endoplasmic reticulum-mitochondria interface and its regulation by the Gp78 ubiquitin ligase
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$100,000
Cihrequipment2
$0
Programname2
Operating Grant - Priority Announcement: Breast Cancer
Keyworddelim
Autocrine Motility Factor; Autophagy; Breast Tumor Progression And Metastasis; Calcium Homeostasis; Er Stress And Cell Death; Er-Mitochondria Interaction; Gp78 Ubiquitin Ligase; P38 Map Kinase; Transgenic Mice
Abstract
Select breast cancers and certain other cancers are more difficult to treat, resulting in devastating diagnoses. Autocrine motility factor (AMF) and its receptor, Gp78, promote tumor cell motility and metastasis and are linked to malignancy in various cancers. Gp78 is found both at the cell surface, where it internalizes AMF from outside the cell, and also inside the cell in the endoplasmic reticulum, where it targets proteins for degradation. Gp78 is found in regions of the endoplasmic reticulum that interact with mitochondria, the energy producing organelle of the cell, where it breaks down mitochondrial proteins and controls the movement and destruction of mitochondria. Both the endoplasmic reticulum and mitochondria play important roles in cell death. We hypothesize that AMF and Gp78 act at the level of these cellular components to promote the survival of tumor cells leading to tumor progression and malignancy.
We will now study how AMF controls Gp78 function in breast cancer and whether AMF control of Gp78 in the endoplasmic reticulum affects its ability to promote tumor malignancy. We made an experimental mouse that expresses elevated levels of Gp78 in breast tissue. We will now generate a mouse that overexpresses AMF in breast tissue and also study mice that lack Gp78. These studies will allow us to determine the relationship between AMF interaction with Gp78 and breast cancer development. We are optimistic that our knowledge translation approach to share research results will enable new mechanistic understandings that will lead to new diagnostic and therapeutic approaches to better treat these potentially terminal cancers and provide a more hopeful prognosis for these cancer patients.
Competitiondate
201503
Approvedterm2
1 yr 0 mth
Pinamesdelim
Nabi, Ivan R
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $100,000~ $0~