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Grant: Doctoral: Vanier Canada Graduate Scholarships

University of Manitoba

$150,000.00

The role of mitophagy and extracellular matrix (ECM) stiffness in the regulation of epithelial-to-mesenchymal transition (EMT), and subsequent metastasis in non-small cell lung cancer (NSCLC) model.

FY 2019-20

Summary
Lung cancer is the main cause of cancer-related deaths in Canada. A major risk for lung cancer deaths is when cancer cells escape the lung to invade other organs, causing new cancers to show up throughout the body. This process is called 'metastasis' and requires the cells to produce lots of extra energy. To supply the energy required for metastasis, cancer cells must first go through major changes in how they recycle old and damaged parts of the cell. A molecule called 'BCL2L13' helps control this recycling process in cancer cells. Importantly, we have found that less of this molecule is made in lung cancer patients whose cancer has spread to other organs. This means that BCL2L13 could help control lung cancer metastasis, and drugs that change BCL2L13 levels might be a good way to treat lung cancer. In my project, I will control the amount of BCL2L13 made in lung cancer cells and examine how it controls the escape of lung cancer cells to other organs. To confirm my results in a more realistic way, I will use an exciting new technology called '3D bioprinting' to build realistic lung cancers in a dish. By controlling the amount of BCL2L13 made in these realistic lung cancers, I can then see how energy production, recycling and metastasis change. Furthermore, we will extend our studies to live human tissue samples from patients with lung cancer. This provides us with extremely useful and first-hand clinical data about lung cancer metastasis and how we can harness BCL2L13 to combat metastasis in patients with lung cancer. Altogether, my project will give us a much better understanding of how BCL2L13 contributes to the spread of lung cancer cells to other organs. This is an important first step towards developing new cancer treatments that target BCL2L13, which will improve the lives of people living with lung cancer.
Program
Doctoral: Vanier Canada Graduate Scholarships
Location
Manitoba, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
415961
Name
Alizadeh Javad
Region
Manitoba
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Vanier Canada Graduate Scholarships CIHR
Projecttitle
The role of mitophagy and extracellular matrix (ECM) stiffness in the regulation of epithelial-to-mesenchymal transition (EMT), and subsequent metastasis in non-small cell lung cancer (NSCLC) model.
Programtype2
Studentship Programs
Orgnameinp2
University of Manitoba
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
Doctoral: Vanier Canada Graduate Scholarships
Keyworddelim
Bcl2 Like Protein 13 (Bcl2l13), Extracellular Matrix (Ecm); Crispr Gene Editing, Orthotopic Mouse Model, 3d Bioprinting; In Vivo Imaging System (Ivis); Lung Cancer, Epithelial-Mesenchymal Transition (Emt); Metastasis, Selective Autophagy, Mitophagy; Non-Small Cell Lung Cancer (Nsclc) Cells; Positron Emission Tomography (Pet)-Magnetic Resonance (Mr); Tissue Collection, Immunoblotting, Immunohistochemistry; Transforming Growth Factor Beta 1 (Tgfß1); Transmission Electron Microscopy, Live-Cell Microscopy
Abstract
Lung cancer is the main cause of cancer-related deaths in Canada. A major risk for lung cancer deaths is when cancer cells escape the lung to invade other organs, causing new cancers to show up throughout the body. This process is called 'metastasis' and requires the cells to produce lots of extra energy. To supply the energy required for metastasis, cancer cells must first go through major changes in how they recycle old and damaged parts of the cell. A molecule called 'BCL2L13' helps control this recycling process in cancer cells. Importantly, we have found that less of this molecule is made in lung cancer patients whose cancer has spread to other organs. This means that BCL2L13 could help control lung cancer metastasis, and drugs that change BCL2L13 levels might be a good way to treat lung cancer. In my project, I will control the amount of BCL2L13 made in lung cancer cells and examine how it controls the escape of lung cancer cells to other organs. To confirm my results in a more realistic way, I will use an exciting new technology called '3D bioprinting' to build realistic lung cancers in a dish. By controlling the amount of BCL2L13 made in these realistic lung cancers, I can then see how energy production, recycling and metastasis change. Furthermore, we will extend our studies to live human tissue samples from patients with lung cancer. This provides us with extremely useful and first-hand clinical data about lung cancer metastasis and how we can harness BCL2L13 to combat metastasis in patients with lung cancer. Altogether, my project will give us a much better understanding of how BCL2L13 contributes to the spread of lung cancer cells to other organs. This is an important first step towards developing new cancer treatments that target BCL2L13, which will improve the lives of people living with lung cancer.
Competitiondate
201911
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Alizadeh, Javad
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~