Abstract A040: Using mitochondrial abundance in tumor-derived extracellular vesicles for pancreatic cancer screening

Abstract Pancreatic cancer, marked by a high mortality rate and rising incidence, often goes undetected until advanced stages, complicating treatment. Tumor-derived extracellular vesicles (EVs) have emerged as promising cancer biomarkers due to their cargo from parent cells. However, current detection methods are often time-consuming, expensive, and complex. To overcome these challenges, we developed a screening assay for pancreatic cancer that uses the mitochondrial DNA to nuclear DNA ratio in tumor-derived EVs as a distinguishing feature. This assay combines immunoprecipitation with qPCR quantification for direct detection of tumor-derived EVs from serum, utilizing DNA-isolation-free techniques and duplexing probes for qPCR, thus saving at least 3 hours. Clinical sample testing demonstrated the assay's potential as a translational tool for cancer screening, showing a weak correlation with prognosis biomarkers and sufficient discriminatory power between healthy controls, pancreatitis, and pancreatic cancer cases. Citation Format: Dali Sun. Using mitochondrial abundance in tumor-derived extracellular vesicles for pancreatic cancer screening [abstract]. In: Proceedings of the AACR Special Conference: Liquid Biopsy: From Discovery to Clinical Implementation; 2024 Nov 13-16; San Diego, CA. Philadelphia (PA): AACR; Clin Cancer Res 2024;30(21_Suppl):Abstract nr A040.

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Journal
Clinical Cancer Research
Published
2024-11-13
DOI
https://doi.org/10.1158/1557-3265.liqbiop24-a040
Primary Topic
Extracellular vesicles in disease
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article
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article

Abstract A040: Using mitochondrial abundance in tumor-derived extracellular vesicles for pancreatic cancer screening

Dali Sun
Clinical Cancer Research
Extracellular vesicles in disease
article

Abstract A040: Using mitochondrial abundance in tumor-derived extracellular vesicles for pancreatic cancer screening

Dali Sun
article en

Abstract

Abstract Pancreatic cancer, marked by a high mortality rate and rising incidence, often goes undetected until advanced stages, complicating treatment. Tumor-derived extracellular vesicles (EVs) have emerged as promising cancer biomarkers due to their cargo from parent cells. However, current detection methods are often time-consuming, expensive, and complex. To overcome these challenges, we developed a screening assay for pancreatic cancer that uses the mitochondrial DNA to nuclear DNA ratio in tumor-derived EVs as a distinguishing feature. This assay combines immunoprecipitation with qPCR quantification for direct detection of tumor-derived EVs from serum, utilizing DNA-isolation-free techniques and duplexing probes for qPCR, thus saving at least 3 hours. Clinical sample testing demonstrated the assay's potential as a translational tool for cancer screening, showing a weak correlation with prognosis biomarkers and sufficient discriminatory power between healthy controls, pancreatitis, and pancreatic cancer cases. Citation Format: Dali Sun. Using mitochondrial abundance in tumor-derived extracellular vesicles for pancreatic cancer screening [abstract]. In: Proceedings of the AACR Special Conference: Liquid Biopsy: From Discovery to Clinical Implementation; 2024 Nov 13-16; San Diego, CA. Philadelphia (PA): AACR; Clin Cancer Res 2024;30(21_Suppl):Abstract nr A040.

Clinical Cancer ResearchVol. 30(21_Supplement)
University of Denver (US)
Openalex Percentile: Top 82%
Extracellular vesicles in disease
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Abstract A040: Using mitochondrial abundance in tumor-derived extracellular vesicles for pancreatic cancer screening — Dali Sun · Clinical Cancer Research (2024) | TGRS Research Map | TGRS