A Fragment of Collagen Type VI alpha-3 chain is Elevated in Serum from Patients with Gastrointestinal Disorders

Signe Holm Nielsen*, Joachim Høg Mortensen, Nicholas Willumsen, Daniel Guldager Kring Rasmussen, Ditte J. Mogensen, Antonio Di Sabatino, Giuseppe Mazza, Lars Nannestad Jørgensen, Paolo Giuffrida, Massimo Pinzani, Lone Klinge, Jens Kjeldsen, Diana Julie Leeming, Morten Asser Karsdal, Federica Genovese

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

169 Downloads (Pure)

Abstract

Extracellular matrix (ECM) remodeling is a hallmark of the pathology of gastrointestinal disorders. Collagen type VI (COL6) is produced by fibroblasts, and the COL6 α3-chain has shown to be elevated in patients with ulcerative colitis (UC), Crohn's disease (CD) and colorectal cancer (CRC). Measuring COL6α3 in serum may therefore have potential as a biomarker for gastrointestinal disorders. The aims of this study were to develop and validate a competitive ELISA targeting a specific neo-epitope of COL6α3 and evaluate its associations with the gastrointestinal disorders UC, CD and CRC, in comparison to healthy controls. A monoclonal antibody was raised against a matrix metalloproteinase-2 and -9 specific cleavage site of COL6α3 (C6Mα3) and employed in a competitive enzyme-linked immunosorbent assay (ELISA). The assay was developed and technically validated. Levels of C6Mα3 were measured in serum from patients with UC (n = 58), CD (n = 44) and CRC (n = 39) and compared to healthy controls (n = 32). The levels of C6Mα3 were elevated in patients with UC, CD and CRC patients compared to healthy controls (all p 
Original languageEnglish
Article number5910
JournalScientific Reports
Volume10
Issue number1
Number of pages8
ISSN2045-2322
DOIs
Publication statusPublished - 2020

Fingerprint

Dive into the research topics of 'A Fragment of Collagen Type VI alpha-3 chain is Elevated in Serum from Patients with Gastrointestinal Disorders'. Together they form a unique fingerprint.

Cite this