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Grant: DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)

Queen's University (Kingston, Ontario)

$120,000.00

Small signals, big impact: Extracellular vesicles reveal functional insights and biomarkers in Endometriosis progression

FY 2025-26

Summary
Endometriosis (EM) is a chronic disease where tissue similar to the uterine lining grows outside the uterus, often on the ovaries, bowel, and bladder. EM affects ~10% of reproductive-age women, impacting 190 million worldwide. Symptoms include pelvic pain and infertility, though severity varies widely. Some patients with severe EM may be symptom-free, while others with mild disease suffer debilitating pain. This variability contributes to misdiagnosis and diagnostic delays, averaging 4-11 years. Diagnosis remains challenging and invasive, relying on direct visualization of lesions through laparoscopic surgery. Yet ~50% of procedures yield negative findings, subjecting patients to unnecessary trauma and delays. Despite its prevalence and impact on quality of life, effective diagnostic and therapeutic strategies remain limited, with no non-invasive or fertility-sparing options. EM disproportionately affects females, intersecting with societal and gender biases that contribute to disparities in care. The cause of endometriosis is not fully understood, but emerging evidence points to improper functioning of the body's immune system and suggests a potential role for small extracellular vesicles (sEVs). sEVs are tiny particles released by cells that carry influential cargo from their cells of origin. sEVs circulate in body fluids, transferring these altered signals to other cells/tissues, which can drive disease progression. Their unique properties make them promising biomarkers for EM. We propose the first in-depth analysis of sEVs in EM, providing a comprehensive molecular profile and exploring their functional roles in disease mechanisms. Using patient samples, cell culture models and mechanistic studies in mice, our study will reveal the utility of these sEVs to identify novel biomarkers specific to EM. This will help prioritize candidates for surgical reconfirmation, reduce unnecessary procedures and ultimately shorten diagnostic delays to improve patient outcomes.
Program
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Location
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
560315
Name
Holmes Jaelis P
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
DT1 (Biomedical and/or Clinical Research) CGRS Doctoral
Projecttitle
Small signals, big impact: Extracellular vesicles reveal functional insights and biomarkers in Endometriosis progression
Programtype2
Studentship Programs
Orgnameinp2
Queen's University (Kingston, Ontario)
Cihramount2
$120,000
Cihrequipment2
$0
Programname2
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Keyworddelim
Biomarkers; Endometriosis; Extracellular Vesicles (Evs); Immune Dysfunction; Molecular Profiling; Non-Invasive Diagnostics; Reproductive Health; Sex And Gender-Based Analysis
Abstract
Endometriosis (EM) is a chronic disease where tissue similar to the uterine lining grows outside the uterus, often on the ovaries, bowel, and bladder. EM affects ~10% of reproductive-age women, impacting 190 million worldwide. Symptoms include pelvic pain and infertility, though severity varies widely. Some patients with severe EM may be symptom-free, while others with mild disease suffer debilitating pain. This variability contributes to misdiagnosis and diagnostic delays, averaging 4-11 years. Diagnosis remains challenging and invasive, relying on direct visualization of lesions through laparoscopic surgery. Yet ~50% of procedures yield negative findings, subjecting patients to unnecessary trauma and delays. Despite its prevalence and impact on quality of life, effective diagnostic and therapeutic strategies remain limited, with no non-invasive or fertility-sparing options. EM disproportionately affects females, intersecting with societal and gender biases that contribute to disparities in care. The cause of endometriosis is not fully understood, but emerging evidence points to improper functioning of the body's immune system and suggests a potential role for small extracellular vesicles (sEVs). sEVs are tiny particles released by cells that carry influential cargo from their cells of origin. sEVs circulate in body fluids, transferring these altered signals to other cells/tissues, which can drive disease progression. Their unique properties make them promising biomarkers for EM. We propose the first in-depth analysis of sEVs in EM, providing a comprehensive molecular profile and exploring their functional roles in disease mechanisms. Using patient samples, cell culture models and mechanistic studies in mice, our study will reveal the utility of these sEVs to identify novel biomarkers specific to EM. This will help prioritize candidates for surgical reconfirmation, reduce unnecessary procedures and ultimately shorten diagnostic delays to improve patient outcomes.
Competitiondate
202511
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Holmes, Jaelis P
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $120,000~ $0~