Grant: Project Grant
McGill University
$990,675.00
Defining the distinct roles of MAPK pathway mutations in immune and targeted therapy response in melanoma
EF 2021-22
Résumé
Skin melanoma is one of the fastest rising cancers. It is also the deadliest form of skin cancer. Melanomas come from melanocytes. These are the cells that cause you to tan when you are exposed to the sun. Melanomas arise when individual melanocytes acquire specific DNA changes, called mutations. Many of these mutations are caused by sun exposure. These mutations allow melanocytes to grow uncontrollably leading to melanoma. For melanomas to continue to grow uncontrollably, they also need to gain the ability to escape being seen from the immune system.
The research community has made significant progress to develop new treatments for patients. These include two types. The first type is a treatment called targeted therapies, which are drugs that specifically kill melanoma cells by targeting mutations that cause melanoma. The second type is a treatment called immune therapy. This type of therapy helps the immune system recognize melanomas as foreign and harnesses the power of a patient's immune system to eliminate melanoma cells.
An important challenge is emerging in clinical practice in deciding between targeted and immune therapies. Some types of mutations lead to better responses to immune therapy and worse to targeted therapy. And vice versa. The first goal of this proposal is to figure out why this is the case. The second goal of this project is to test new drugs against mutations that lead to therapy resistance. We hope that the work performed in this proposal will provide doctors with knowledge to help them prescribe the right drug at the right time, and the ability to prescribe new drugs to overcome therapy resistance.
Programme
Project Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
452693
Name
Watson Ian R
Region
Québec
Country
Canada
Orgtype
Research Institution; Institution Paid
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Progression & Therapeutics
Projecttitle
Defining the distinct roles of MAPK pathway mutations in immune and targeted therapy response in melanoma
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$990,675
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Braf; Cell Signalling; Cutaneous Melanoma; Immune Checkpoint Inhibitors; Mapk Pathway; Mouse Models Of Cancer; Nf1; Nras; Pd-L1; Targeted Therapy
Abstract
Skin melanoma is one of the fastest rising cancers. It is also the deadliest form of skin cancer. Melanomas come from melanocytes. These are the cells that cause you to tan when you are exposed to the sun. Melanomas arise when individual melanocytes acquire specific DNA changes, called mutations. Many of these mutations are caused by sun exposure. These mutations allow melanocytes to grow uncontrollably leading to melanoma. For melanomas to continue to grow uncontrollably, they also need to gain the ability to escape being seen from the immune system.
The research community has made significant progress to develop new treatments for patients. These include two types. The first type is a treatment called targeted therapies, which are drugs that specifically kill melanoma cells by targeting mutations that cause melanoma. The second type is a treatment called immune therapy. This type of therapy helps the immune system recognize melanomas as foreign and harnesses the power of a patient's immune system to eliminate melanoma cells.
An important challenge is emerging in clinical practice in deciding between targeted and immune therapies. Some types of mutations lead to better responses to immune therapy and worse to targeted therapy. And vice versa. The first goal of this proposal is to figure out why this is the case. The second goal of this project is to test new drugs against mutations that lead to therapy resistance. We hope that the work performed in this proposal will provide doctors with knowledge to help them prescribe the right drug at the right time, and the ability to prescribe new drugs to overcome therapy resistance.
Competitiondate
202109
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Watson, Ian R
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $990,675~ $0~