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Ascites-derived CDCP1+ extracellular vesicles subcluster as a novel biomarker and therapeutic target for ovarian cancer

INTRODUCTION: Ovarian cancer (OVCA) is one of the most prevalent malignant tumors of the female reproductive system, and its diagnosis is typically accompanied by the production of ascites. Although liquid biopsy has been widely implemented recently, the diagnosis or prognosis of OVCA based on liqui...

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Autores principales: Kong, Lingnan, Xu, Famei, Yao, Yukuan, Gao, Zhihui, Tian, Peng, Zhuang, Shichao, Wu, Di, Li, Tangyue, Cai, Yanling, Li, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352483/
https://www.ncbi.nlm.nih.gov/pubmed/37469398
http://dx.doi.org/10.3389/fonc.2023.1142755
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author Kong, Lingnan
Xu, Famei
Yao, Yukuan
Gao, Zhihui
Tian, Peng
Zhuang, Shichao
Wu, Di
Li, Tangyue
Cai, Yanling
Li, Jing
author_facet Kong, Lingnan
Xu, Famei
Yao, Yukuan
Gao, Zhihui
Tian, Peng
Zhuang, Shichao
Wu, Di
Li, Tangyue
Cai, Yanling
Li, Jing
author_sort Kong, Lingnan
collection PubMed
description INTRODUCTION: Ovarian cancer (OVCA) is one of the most prevalent malignant tumors of the female reproductive system, and its diagnosis is typically accompanied by the production of ascites. Although liquid biopsy has been widely implemented recently, the diagnosis or prognosis of OVCA based on liquid biopsy remains the primary emphasis. METHODS: In this study, using proximity barcoding assay, a technique for analyzing the surface proteins on single extracellular vesicles (EVs). For validation, serum and ascites samples from patients with epithelial ovarian cancer (EOC) were collected, and their levels of CDCP1 was determined by enzyme-linked immunosorbent assay. Tissue chips were prepared to analyze the relationship between different expression levels of CDCP1 and the prognosis of ovarian cancer patients. RESULTS: We discovered that the CUB domain-containing protein 1+ (CDCP1+) EVs subcluster was higher in the ascites of OVCA patients compared to benign ascites. At the same time, the level of CDCP1 was considerably elevated in the ascites of OVCA patients. The overall survival and disease-free survival of the group with high CDCP1 expression in EOC were significantly lower than those of the group with low expression. In addition, the receiver operating characteristic curve demonstrates that EVs-derived CDCP1 was a biomarker of early response in OVCA ascites. DISCUSSION: Our findings identified a CDCP1+ EVs subcluster in the ascites of OVCA patients as a possible biomarker for EOC prevention.
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spelling pubmed-103524832023-07-19 Ascites-derived CDCP1+ extracellular vesicles subcluster as a novel biomarker and therapeutic target for ovarian cancer Kong, Lingnan Xu, Famei Yao, Yukuan Gao, Zhihui Tian, Peng Zhuang, Shichao Wu, Di Li, Tangyue Cai, Yanling Li, Jing Front Oncol Oncology INTRODUCTION: Ovarian cancer (OVCA) is one of the most prevalent malignant tumors of the female reproductive system, and its diagnosis is typically accompanied by the production of ascites. Although liquid biopsy has been widely implemented recently, the diagnosis or prognosis of OVCA based on liquid biopsy remains the primary emphasis. METHODS: In this study, using proximity barcoding assay, a technique for analyzing the surface proteins on single extracellular vesicles (EVs). For validation, serum and ascites samples from patients with epithelial ovarian cancer (EOC) were collected, and their levels of CDCP1 was determined by enzyme-linked immunosorbent assay. Tissue chips were prepared to analyze the relationship between different expression levels of CDCP1 and the prognosis of ovarian cancer patients. RESULTS: We discovered that the CUB domain-containing protein 1+ (CDCP1+) EVs subcluster was higher in the ascites of OVCA patients compared to benign ascites. At the same time, the level of CDCP1 was considerably elevated in the ascites of OVCA patients. The overall survival and disease-free survival of the group with high CDCP1 expression in EOC were significantly lower than those of the group with low expression. In addition, the receiver operating characteristic curve demonstrates that EVs-derived CDCP1 was a biomarker of early response in OVCA ascites. DISCUSSION: Our findings identified a CDCP1+ EVs subcluster in the ascites of OVCA patients as a possible biomarker for EOC prevention. Frontiers Media S.A. 2023-07-03 /pmc/articles/PMC10352483/ /pubmed/37469398 http://dx.doi.org/10.3389/fonc.2023.1142755 Text en Copyright © 2023 Kong, Xu, Yao, Gao, Tian, Zhuang, Wu, Li, Cai and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Kong, Lingnan
Xu, Famei
Yao, Yukuan
Gao, Zhihui
Tian, Peng
Zhuang, Shichao
Wu, Di
Li, Tangyue
Cai, Yanling
Li, Jing
Ascites-derived CDCP1+ extracellular vesicles subcluster as a novel biomarker and therapeutic target for ovarian cancer
title Ascites-derived CDCP1+ extracellular vesicles subcluster as a novel biomarker and therapeutic target for ovarian cancer
title_full Ascites-derived CDCP1+ extracellular vesicles subcluster as a novel biomarker and therapeutic target for ovarian cancer
title_fullStr Ascites-derived CDCP1+ extracellular vesicles subcluster as a novel biomarker and therapeutic target for ovarian cancer
title_full_unstemmed Ascites-derived CDCP1+ extracellular vesicles subcluster as a novel biomarker and therapeutic target for ovarian cancer
title_short Ascites-derived CDCP1+ extracellular vesicles subcluster as a novel biomarker and therapeutic target for ovarian cancer
title_sort ascites-derived cdcp1+ extracellular vesicles subcluster as a novel biomarker and therapeutic target for ovarian cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352483/
https://www.ncbi.nlm.nih.gov/pubmed/37469398
http://dx.doi.org/10.3389/fonc.2023.1142755
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