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Proteomic Analyses of Fibroblast- and Serum-Derived Exosomes Identify QSOX1 as a Marker for Non-Invasive Detection of Colorectal Cancer

Title: Proteomic Analyses of Fibroblast- and Serum-Derived Exosomes Identify QSOX1 as a Marker for Non-Invasive Detection of Colorectal Cancer
Authors: Nicole Ganig; Franziska Baenke; May-Linn Thepkaysone; Kuailu Lin; Venkatesh S. Rao; Fang Cheng Wong; Heike Polster; Martin Schneider; Dominic Helm; Mathieu Pecqueux; Adrian M. Seifert; Lena Seifert; Jürgen Weitz; Nuh N. Rahbari; Christoph Kahlert
Source: Cancers, Vol 13, Iss 1351, p 1351 (2021)
Publisher Information: MDPI AG
Publication Year: 2021
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: colorectal cancer; tumour microenvironment; cancer-associated fibroblasts; extracellular vesicles; exosomes; liquid biopsy; Neoplasms. Tumors. Oncology. Including cancer and carcinogens; RC254-282
Description: The treatment of colorectal cancer (CRC) has improved during the last decades, but methods for crucial early diagnosis are yet to be developed. The influence of the tumour microenvironment on liquid biopsies for early cancer diagnostics are gaining growing interest, especially with emphasis on exosomes (EXO), a subgroup of extracellular vesicles (EVs). In this study, we established paired cancer-associated (CAFs) and normal fibroblasts (NF) from 13 CRC patients and investigated activation status-related protein abundance in derived EXOs. Immunohistochemical staining of matched patient tissue was performed and an independent test cohort of CRC patient plasma-derived EXOs was assessed by ELISA. A total of 11 differentially abundant EV proteins were identified between NFs and CAFs. In plasma EXOs, the CAF-EXO enriched protein EDIL3 was elevated, while the NF-EXO enriched protein QSOX1 was diminished compared to whole plasma. Both markers were significantly reduced in patient-matched CRC tissue compared to healthy colon tissue. In an independent test cohort, a significantly reduced protein abundance of QSOX1 was observed in plasma EXOs from CRC patients compared to controls and diagnostic ROC curve analysis revealed an AUC of 0.904. In conclusion, EXO-associated QSOX1 is a promising novel marker for early diagnosis and non-invasive risk stratification in CRC.
Document Type: article in journal/newspaper
Language: English
Relation: https://www.mdpi.com/2072-6694/13/6/1351; https://doaj.org/toc/2072-6694; https://doaj.org/article/0fa3b37195d942ad88983a7ea725c9f9
DOI: 10.3390/cancers13061351
Availability: https://doi.org/10.3390/cancers13061351; https://doaj.org/article/0fa3b37195d942ad88983a7ea725c9f9
Accession Number: edsbas.58F7D94A
Database: BASE