Canada Spends Logo

Explore our Budget 2026 analysis

Grant: Collaborative Health Research Projects

Ma, Hongshen (The University of British Columbia)

$489,780.00

Development of Technologies for Rapid Isolation and Genome Sequencing of Single Circulating Tumor Cells in Prostate Cancer

EF 2017-18 · 2017-04-25

Résumé
The vast majority of cancer deaths are caused by metastasis, or the spread of cancer from_x000D_ one part of the body to another. In order for cancer to spread, cells known as circulating tumor_x000D_ cells, must detach from a tumor, circulate in the bloodstream, and reattach to a different_x000D_ tissue. Therefore, circulating tumor cells are considered to be the agents of metastasis that_x000D_ could potentially be used to evaluate the genetic basis of each patients cancer and how they_x000D_ might respond to potential treatments. Genetic analysis of circulating tumor cells is currently_x000D_ limited by the extreme rarity of these cells in the bloodstream, as well as by the differences_x000D_ across individual cells. This project aims to address this challenge by developing a technology_x000D_ to rapidly isolate individual circulating tumor cells for genome sequencing. We will then test_x000D_ this technology by isolating and sequencing single circulating tumor cells from patients with_x000D_ advanced prostate cancer who are currently enrolled in related clinical studies. The genome_x000D_ sequence from single circulating tumor cells will then be compared with other available data in_x000D_ order to determine its value in diagnosis and treatment. Genome sequencing is already being_x000D_ used in some cancers to predict how patients will respond to certain drugs. This project will_x000D_ develop a technology to isolate and sequence cells that are most relevant to metastasis,_x000D_ which will give physicians significantly better information to evaluate each patients disease in_x000D_ order to devise a personalized treatment plan.
Programme
Collaborative Health Research Projects
Emplacement
British Columbia|Colombie-Britannique, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
Proactive Disclosure - Grants and Contributions

Tel que publié

Additional Information
Grant or Award spanning more than one fiscal year. (2017-2018 to 2020-2021)
Additional Information (French)
Subvention ou bourse octroyée s'appliquant à plus d'un exercice financier. (2017-2018 à 2020-2021)
Agreement Number
CHRPJ
Agreement Start Date
2017-04-25
Agreement Title
Development of Technologies for Rapid Isolation and Genome Sequencing of Single Circulating Tumor Cells in Prostate Cancer
Agreement Title (French)
Development of Technologies for Rapid Isolation and Genome Sequencing of Single Circulating Tumor Cells in Prostate Cancer
Agreement Type
Grant
Agreement Value
$489,780.00
Amendment Number
0
Organization Code
nserc-crsng
Organization
Natural Sciences and Engineering Research Council of Canada | Conseil de recherches en sciences naturelles et en génie du Canada
Program Name
Collaborative Health Research Projects
Program Name (French)
Projets de recherche concertée sur la santé
Program Purpose
The vast majority of cancer deaths are caused by metastasis, or the spread of cancer from_x000D_ one part of the body to another. In order for cancer to spread, cells known as circulating tumor_x000D_ cells, must detach from a tumor, circulate in the bloodstream, and reattach to a different_x000D_ tissue. Therefore, circulating tumor cells are considered to be the agents of metastasis that_x000D_ could potentially be used to evaluate the genetic basis of each patients cancer and how they_x000D_ might respond to potential treatments. Genetic analysis of circulating tumor cells is currently_x000D_ limited by the extreme rarity of these cells in the bloodstream, as well as by the differences_x000D_ across individual cells. This project aims to address this challenge by developing a technology_x000D_ to rapidly isolate individual circulating tumor cells for genome sequencing. We will then test_x000D_ this technology by isolating and sequencing single circulating tumor cells from patients with_x000D_ advanced prostate cancer who are currently enrolled in related clinical studies. The genome_x000D_ sequence from single circulating tumor cells will then be compared with other available data in_x000D_ order to determine its value in diagnosis and treatment. Genome sequencing is already being_x000D_ used in some cancers to predict how patients will respond to certain drugs. This project will_x000D_ develop a technology to isolate and sequence cells that are most relevant to metastasis,_x000D_ which will give physicians significantly better information to evaluate each patients disease in_x000D_ order to devise a personalized treatment plan.
Program Purpose (French)
The vast majority of cancer deaths are caused by metastasis, or the spread of cancer from_x000D_ one part of the body to another. In order for cancer to spread, cells known as circulating tumor_x000D_ cells, must detach from a tumor, circulate in the bloodstream, and reattach to a different_x000D_ tissue. Therefore, circulating tumor cells are considered to be the agents of metastasis that_x000D_ could potentially be used to evaluate the genetic basis of each patients cancer and how they_x000D_ might respond to potential treatments. Genetic analysis of circulating tumor cells is currently_x000D_ limited by the extreme rarity of these cells in the bloodstream, as well as by the differences_x000D_ across individual cells. This project aims to address this challenge by developing a technology_x000D_ to rapidly isolate individual circulating tumor cells for genome sequencing. We will then test_x000D_ this technology by isolating and sequencing single circulating tumor cells from patients with_x000D_ advanced prostate cancer who are currently enrolled in related clinical studies. The genome_x000D_ sequence from single circulating tumor cells will then be compared with other available data in_x000D_ order to determine its value in diagnosis and treatment. Genome sequencing is already being_x000D_ used in some cancers to predict how patients will respond to certain drugs. This project will_x000D_ develop a technology to isolate and sequence cells that are most relevant to metastasis,_x000D_ which will give physicians significantly better information to evaluate each patients disease in_x000D_ order to devise a personalized treatment plan.
Recipient City
British Columbia|Colombie-Britannique
Recipient Country
CA
Recipient Legal Name
Ma, Hongshen (The University of British Columbia)
Reference Number
GC-2017-Q1-00260