TY - GEN N2 - This thesis work highlights development and applications for both circulating extracellular vesicles (EV) and cell-free RNA (cf-RNA) toward liquid biopsy based early cancer detection methodologies. Effective detection and monitoring for signatures of oncological disease in a noninvasive manner are urgently needed to reduce the morbidity and mortality caused by cancer. Circulating EVs and cf-RNA are intensely sought after biomarkers in liquid biopsy. Their roles in cell-to-cell communication, ability to reflect phenotypic changes from cells, and tissues of origin are becoming better understood. Despite this, current literatures present key challenges which limit the promise of liquid biopsy based early cancer detection: i) there is a lack of standardized blood processing for multi-omics which minimizes ex-vivo processing artefacts via discerning true in-vivo signatures from ex-vivo artefacts; ii) daily fluctuations and the influence of meal consumption on EV and cf-RNA levels are not clear; iii) a comprehensive study of cf-RNA for cancer detection, pan cancer discernment, and high risk group identification has not been conducted; and iv) the selective packaging of cf-RNA carriers and its association with cancer are unknown. DO - 10.6083/xs55mc819 DO - DOI AB - This thesis work highlights development and applications for both circulating extracellular vesicles (EV) and cell-free RNA (cf-RNA) toward liquid biopsy based early cancer detection methodologies. Effective detection and monitoring for signatures of oncological disease in a noninvasive manner are urgently needed to reduce the morbidity and mortality caused by cancer. Circulating EVs and cf-RNA are intensely sought after biomarkers in liquid biopsy. Their roles in cell-to-cell communication, ability to reflect phenotypic changes from cells, and tissues of origin are becoming better understood. Despite this, current literatures present key challenges which limit the promise of liquid biopsy based early cancer detection: i) there is a lack of standardized blood processing for multi-omics which minimizes ex-vivo processing artefacts via discerning true in-vivo signatures from ex-vivo artefacts; ii) daily fluctuations and the influence of meal consumption on EV and cf-RNA levels are not clear; iii) a comprehensive study of cf-RNA for cancer detection, pan cancer discernment, and high risk group identification has not been conducted; and iv) the selective packaging of cf-RNA carriers and its association with cancer are unknown. T1 - Discovery of early cancer signatures in circulating RNA and extracellular vesicles DA - 2021 AU - Kim, Hyun J. L1 - https://digitalcollections.ohsu.edu/record/9098/files/Kim.Hyun.Ji.2021.pdf PB - Oregon Health and Science University PY - 2021 ID - 9098 L4 - https://digitalcollections.ohsu.edu/record/9098/files/Kim.Hyun.Ji.2021.pdf KW - Extracellular Vesicles KW - Neoplasms KW - Biomarkers KW - Liquid Biopsy KW - Cell-Free Nucleic Acids KW - messenger rna TI - Discovery of early cancer signatures in circulating RNA and extracellular vesicles Y1 - 2021 L2 - https://digitalcollections.ohsu.edu/record/9098/files/Kim.Hyun.Ji.2021.pdf LK - https://digitalcollections.ohsu.edu/record/9098/files/Kim.Hyun.Ji.2021.pdf UR - https://digitalcollections.ohsu.edu/record/9098/files/Kim.Hyun.Ji.2021.pdf ER -