PCPE2: Expression of Multifunctional Extracellular Glycoprotein Associates With Diverse Cellular Functions.
Cancer
Diabetes
Fibrosis
Inflammation
Lipid Metabolism
PCOLCE
PCOLCE2
PCPE
PCPE2
Procollagen C-endopeptidase enhancer 2
Wound Healing
Journal
Journal of lipid research
ISSN: 1539-7262
Titre abrégé: J Lipid Res
Pays: United States
ID NLM: 0376606
Informations de publication
Date de publication:
05 Oct 2024
05 Oct 2024
Historique:
received:
31
03
2024
revised:
21
09
2024
accepted:
01
10
2024
medline:
8
10
2024
pubmed:
8
10
2024
entrez:
7
10
2024
Statut:
aheadofprint
Résumé
Procollagen C-endopeptidase enhancer 2, known as PCPE2 or PCOC2 (gene name, PCOLCE2) is a glycoprotein that resides in the extracellular matrix, and is similar in domain organization to PCPE1 / PCPE, PCOC1 (PCOLCE1 /PCOLCE). Due to the many similarities between the two related proteins, PCPE2 has been assumed to have biological functions similar to PCPE. PCPE is a well-established enhancer of procollagen processing activating the enzyme, BMP-1. However, reports show that PCPE2 has a strikingly different tissue expression profile compared to PCPE. With that in mind and given the paucity of published studies on PCPE2, this review examines the current literature citing PCPE2 and its association with specific cell types and signaling pathways. Additionally, this review will present a brief history of PCPE2's discovery, highlighting structural and functional similarities and differences compared to PCPE. Considering the widespread use of RNA sequencing techniques to examine associations between cell-specific gene expression and disease states, we will show that PCPE2 is repeatedly found as a differentially regulated gene (DEG) significantly associated with a number of cellular processes, well beyond the scope of procollagen fibril processing.
Identifiants
pubmed: 39374805
pii: S0022-2275(24)00169-X
doi: 10.1016/j.jlr.2024.100664
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
100664Informations de copyright
Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.