Grant: Doctoral Research Award: Canada Graduate Scholarships
University of British Columbia
$105,000.00
An Improved Culture Protocol for Patient-Derived Multiple Myeloma Cells
FY 2021-22
Summary
Multiple myeloma (MM) is a prevalent and incurable blood cancer with poor prognosis and a high rate of relapse. It presents a dire unmet need in its understanding as a disease and an urgency to improve outcomes through the pursuit of new treatment avenues. Studying MM with patient-derived cells is far superior and more biologically relevant compared to immortalized cell lines purchased from biological resource centres. However, this remains a challenge as current primary MM culturing techniques are incapable of maintaining cell viability for a duration long enough to conduct meaningful experiments. Therefore, it is crucial to urgently establish a new and effective protocol for keeping primary myeloma cells alive and to support their growth. Preliminary work has been conducted to identify the most relevant MM markers and to test various culture conditions with different growth media and environmental factors. The first aim is to determine which cytokines, substances secreted by some immune cells for cell signalling, are required for growth and survival by conducting a cytokine screen aided by a bioinformatic approach, which will then supplement the culture media. Results will be measured by growth, survival and retention of MM characteristics. In addition, the second aim is to conduct a small-molecule screen to further identify the compounds necessary to maintain MM cell viability and growth in vitro. Evaluation of the culture protocol from Aims 1/2 will be conducted in Aim 3, which is to apply these conditions in optimizing the culture of mouse model cells. This protocol must be simple, controllable, reproducible and compatible with high-throughput experiments to remove accessibility barriers experienced by researchers. Creation and establishment of such a protocol will aid the treatment of MM and provide possibilities for rapid development of novel and more specific therapies.
Department
Program
Doctoral Research Award: Canada Graduate Scholarships
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
459071
Name
Cabantog Ariene D
Region
British Columbia
Country
Canada
Orgtype
Research Institution; Institution Paid
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
An Improved Culture Protocol for Patient-Derived Multiple Myeloma Cells
Programtype2
Studentship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Research Award: Canada Graduate Scholarships
Keyworddelim
Bone Marrow; Cancer; Cell Culture; Cell Signalling; Chronic Disease; Cytokines; Disease Model; Microenvironment; Multiple Myeloma; Primary Sample
Abstract
Multiple myeloma (MM) is a prevalent and incurable blood cancer with poor prognosis and a high rate of relapse. It presents a dire unmet need in its understanding as a disease and an urgency to improve outcomes through the pursuit of new treatment avenues. Studying MM with patient-derived cells is far superior and more biologically relevant compared to immortalized cell lines purchased from biological resource centres. However, this remains a challenge as current primary MM culturing techniques are incapable of maintaining cell viability for a duration long enough to conduct meaningful experiments. Therefore, it is crucial to urgently establish a new and effective protocol for keeping primary myeloma cells alive and to support their growth. Preliminary work has been conducted to identify the most relevant MM markers and to test various culture conditions with different growth media and environmental factors. The first aim is to determine which cytokines, substances secreted by some immune cells for cell signalling, are required for growth and survival by conducting a cytokine screen aided by a bioinformatic approach, which will then supplement the culture media. Results will be measured by growth, survival and retention of MM characteristics. In addition, the second aim is to conduct a small-molecule screen to further identify the compounds necessary to maintain MM cell viability and growth in vitro. Evaluation of the culture protocol from Aims 1/2 will be conducted in Aim 3, which is to apply these conditions in optimizing the culture of mouse model cells. This protocol must be simple, controllable, reproducible and compatible with high-throughput experiments to remove accessibility barriers experienced by researchers. Creation and establishment of such a protocol will aid the treatment of MM and provide possibilities for rapid development of novel and more specific therapies.
Competitiondate
202111
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Cabantog, Ariene D
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~