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Serum extracellular vesicles contain SPARC and LRG1 as biomarkers of colon cancer and differ by tumour primary location

BACKGROUND: Recently, the distinction between left- and right-sided colon cancer (LCC and RCC) has been brought into focus. RCC is associated with an inferior overall survival and progression-free survival. We aimed to perform a detailed analysis of the diversity of extracellular vesicles (EV) betwe...

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Autores principales: Zhong, Min-Er, Chen, Yanyu, Xiao, Yi, Xu, Lai, Zhang, Guannan, Lu, Junyang, Qiu, Huizhong, Ge, Wei, Wu, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921233/
https://www.ncbi.nlm.nih.gov/pubmed/31753726
http://dx.doi.org/10.1016/j.ebiom.2019.11.003
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author Zhong, Min-Er
Chen, Yanyu
Xiao, Yi
Xu, Lai
Zhang, Guannan
Lu, Junyang
Qiu, Huizhong
Ge, Wei
Wu, Bin
author_facet Zhong, Min-Er
Chen, Yanyu
Xiao, Yi
Xu, Lai
Zhang, Guannan
Lu, Junyang
Qiu, Huizhong
Ge, Wei
Wu, Bin
author_sort Zhong, Min-Er
collection PubMed
description BACKGROUND: Recently, the distinction between left- and right-sided colon cancer (LCC and RCC) has been brought into focus. RCC is associated with an inferior overall survival and progression-free survival. We aimed to perform a detailed analysis of the diversity of extracellular vesicles (EV) between LCC and RCC using quantitative proteomics and to identify for new diagnostic and prognostic biomarkers. METHODS: We isolated EVs from patients with LCC, RCC and healthy volunteers, and treated colorectal cancer cell line with serum-derived EVs. We then performed a quantitative proteomics analysis of the serum-derived EVs and cell line treated with EVs. Proteomic data are available via ProteomeXchange with the identifiers PXD012283 and PXD012304. In addition, we assessed the performance of EV SPARC and LRG1 as diagnosis and prognosis biomarkers in colon cancer. FINDINGS: The expression profile of the serum EV proteome in patients with RCC was different from that of patients with LCC. Serum-derived EVs in RCC promoted cellular mobility more significantly than EVs derived from LCC. EV SPARC and LRG1 expression levels demonstrated area under the receiver-operating characteristic curve values of 0.95 and 0.93 for discriminating patients with colon cancer from healthy controls. Moreover, the expression levels of SPARC and LRG1 correlated with tumour sidedness and were predictive of tumour recurrence. INTERPRETATION: We identified differences in EV protein profiles between LCC and RCC. Serum-derived EVs of RCC may promote metastasis via upregulation of extracellular matrix (ECM)-related proteins, especially SPARC and LRG1, which may serve as diagnosis and prognosis biomarkers in colon cancer.
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spelling pubmed-69212332019-12-27 Serum extracellular vesicles contain SPARC and LRG1 as biomarkers of colon cancer and differ by tumour primary location Zhong, Min-Er Chen, Yanyu Xiao, Yi Xu, Lai Zhang, Guannan Lu, Junyang Qiu, Huizhong Ge, Wei Wu, Bin EBioMedicine Research paper BACKGROUND: Recently, the distinction between left- and right-sided colon cancer (LCC and RCC) has been brought into focus. RCC is associated with an inferior overall survival and progression-free survival. We aimed to perform a detailed analysis of the diversity of extracellular vesicles (EV) between LCC and RCC using quantitative proteomics and to identify for new diagnostic and prognostic biomarkers. METHODS: We isolated EVs from patients with LCC, RCC and healthy volunteers, and treated colorectal cancer cell line with serum-derived EVs. We then performed a quantitative proteomics analysis of the serum-derived EVs and cell line treated with EVs. Proteomic data are available via ProteomeXchange with the identifiers PXD012283 and PXD012304. In addition, we assessed the performance of EV SPARC and LRG1 as diagnosis and prognosis biomarkers in colon cancer. FINDINGS: The expression profile of the serum EV proteome in patients with RCC was different from that of patients with LCC. Serum-derived EVs in RCC promoted cellular mobility more significantly than EVs derived from LCC. EV SPARC and LRG1 expression levels demonstrated area under the receiver-operating characteristic curve values of 0.95 and 0.93 for discriminating patients with colon cancer from healthy controls. Moreover, the expression levels of SPARC and LRG1 correlated with tumour sidedness and were predictive of tumour recurrence. INTERPRETATION: We identified differences in EV protein profiles between LCC and RCC. Serum-derived EVs of RCC may promote metastasis via upregulation of extracellular matrix (ECM)-related proteins, especially SPARC and LRG1, which may serve as diagnosis and prognosis biomarkers in colon cancer. Elsevier 2019-11-18 /pmc/articles/PMC6921233/ /pubmed/31753726 http://dx.doi.org/10.1016/j.ebiom.2019.11.003 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research paper
Zhong, Min-Er
Chen, Yanyu
Xiao, Yi
Xu, Lai
Zhang, Guannan
Lu, Junyang
Qiu, Huizhong
Ge, Wei
Wu, Bin
Serum extracellular vesicles contain SPARC and LRG1 as biomarkers of colon cancer and differ by tumour primary location
title Serum extracellular vesicles contain SPARC and LRG1 as biomarkers of colon cancer and differ by tumour primary location
title_full Serum extracellular vesicles contain SPARC and LRG1 as biomarkers of colon cancer and differ by tumour primary location
title_fullStr Serum extracellular vesicles contain SPARC and LRG1 as biomarkers of colon cancer and differ by tumour primary location
title_full_unstemmed Serum extracellular vesicles contain SPARC and LRG1 as biomarkers of colon cancer and differ by tumour primary location
title_short Serum extracellular vesicles contain SPARC and LRG1 as biomarkers of colon cancer and differ by tumour primary location
title_sort serum extracellular vesicles contain sparc and lrg1 as biomarkers of colon cancer and differ by tumour primary location
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921233/
https://www.ncbi.nlm.nih.gov/pubmed/31753726
http://dx.doi.org/10.1016/j.ebiom.2019.11.003
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