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Lineage specific extracellular vesicle-associated protein biomarkers for the early detection of high grade serous ovarian cancer
High grade serous ovarian carcinoma (HGSOC) accounts for ~ 70% of ovarian cancer cases. Non-invasive, highly specific blood-based tests for pre-symptomatic screening in women are crucial to reducing the mortality associated with this disease. Since most HGSOCs typically arise from the fallopian tube...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10187430/ https://www.ncbi.nlm.nih.gov/pubmed/37205573 http://dx.doi.org/10.21203/rs.3.rs-2814022/v1 |
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author | Trinidad, Camille Pathak, Harsh Cheng, Shibo Tzeng, Shin-Cheng Madan, Rashna Sardiu, Mihaela Bantis, Leonidas Deighan, Clayton Jewell, Andrea Zeng, Yong Godwin, Andrew |
author_facet | Trinidad, Camille Pathak, Harsh Cheng, Shibo Tzeng, Shin-Cheng Madan, Rashna Sardiu, Mihaela Bantis, Leonidas Deighan, Clayton Jewell, Andrea Zeng, Yong Godwin, Andrew |
author_sort | Trinidad, Camille |
collection | PubMed |
description | High grade serous ovarian carcinoma (HGSOC) accounts for ~ 70% of ovarian cancer cases. Non-invasive, highly specific blood-based tests for pre-symptomatic screening in women are crucial to reducing the mortality associated with this disease. Since most HGSOCs typically arise from the fallopian tubes (FT), our biomarker search focused on proteins found on the surface of extracellular vesicles (EVs) released by both FT and HGSOC tissue explants and representative cell lines. Using mass spectrometry, 985 EV proteins (exo-proteins) were identified that comprised the FT/HGSOC EV core proteome. Transmembrane exo-proteins were prioritized because these could serve as antigens for capture and/or detection. With a nano-engineered microfluidic platform, six newly discovered exo-proteins (ACSL4, IGSF8, ITGA2, ITGA5, ITGB3, MYOF) plus a known HGSOC associated protein, FOLR1 exhibited classification performance ranging from 85–98% in a case-control study using plasma samples representative of early (including stage IA/B) and late stage (stage III) HGSOCs. Furthermore, by linear combination of IGSF8 and ITGA5 based on logistic regression analysis, we achieved a sensitivity of 80% (99.8% specificity). These lineage-associated exo-biomarkers have potential to detect cancer while localized to the FT when patient outcomes are more favorable. |
format | Online Article Text |
id | pubmed-10187430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
spelling | pubmed-101874302023-05-17 Lineage specific extracellular vesicle-associated protein biomarkers for the early detection of high grade serous ovarian cancer Trinidad, Camille Pathak, Harsh Cheng, Shibo Tzeng, Shin-Cheng Madan, Rashna Sardiu, Mihaela Bantis, Leonidas Deighan, Clayton Jewell, Andrea Zeng, Yong Godwin, Andrew Res Sq Article High grade serous ovarian carcinoma (HGSOC) accounts for ~ 70% of ovarian cancer cases. Non-invasive, highly specific blood-based tests for pre-symptomatic screening in women are crucial to reducing the mortality associated with this disease. Since most HGSOCs typically arise from the fallopian tubes (FT), our biomarker search focused on proteins found on the surface of extracellular vesicles (EVs) released by both FT and HGSOC tissue explants and representative cell lines. Using mass spectrometry, 985 EV proteins (exo-proteins) were identified that comprised the FT/HGSOC EV core proteome. Transmembrane exo-proteins were prioritized because these could serve as antigens for capture and/or detection. With a nano-engineered microfluidic platform, six newly discovered exo-proteins (ACSL4, IGSF8, ITGA2, ITGA5, ITGB3, MYOF) plus a known HGSOC associated protein, FOLR1 exhibited classification performance ranging from 85–98% in a case-control study using plasma samples representative of early (including stage IA/B) and late stage (stage III) HGSOCs. Furthermore, by linear combination of IGSF8 and ITGA5 based on logistic regression analysis, we achieved a sensitivity of 80% (99.8% specificity). These lineage-associated exo-biomarkers have potential to detect cancer while localized to the FT when patient outcomes are more favorable. American Journal Experts 2023-05-03 /pmc/articles/PMC10187430/ /pubmed/37205573 http://dx.doi.org/10.21203/rs.3.rs-2814022/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Trinidad, Camille Pathak, Harsh Cheng, Shibo Tzeng, Shin-Cheng Madan, Rashna Sardiu, Mihaela Bantis, Leonidas Deighan, Clayton Jewell, Andrea Zeng, Yong Godwin, Andrew Lineage specific extracellular vesicle-associated protein biomarkers for the early detection of high grade serous ovarian cancer |
title | Lineage specific extracellular vesicle-associated protein biomarkers for the early detection of high grade serous ovarian cancer |
title_full | Lineage specific extracellular vesicle-associated protein biomarkers for the early detection of high grade serous ovarian cancer |
title_fullStr | Lineage specific extracellular vesicle-associated protein biomarkers for the early detection of high grade serous ovarian cancer |
title_full_unstemmed | Lineage specific extracellular vesicle-associated protein biomarkers for the early detection of high grade serous ovarian cancer |
title_short | Lineage specific extracellular vesicle-associated protein biomarkers for the early detection of high grade serous ovarian cancer |
title_sort | lineage specific extracellular vesicle-associated protein biomarkers for the early detection of high grade serous ovarian cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10187430/ https://www.ncbi.nlm.nih.gov/pubmed/37205573 http://dx.doi.org/10.21203/rs.3.rs-2814022/v1 |
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