Matricellular proteins and survival in patients with pancreatic cancer: A systematic review

Pancreatology. 2018 Jan;18(1):122-132. doi: 10.1016/j.pan.2017.11.001. Epub 2017 Nov 4.

Abstract

Extracellular matrix (ECM) plays a fundamental role in tissue architecture and homeostasis and modulates cell functions through a complex interaction between cell surface receptors, hormones, several bioeffector molecules, and structural proteins like collagen. These components are secreted into ECM and all together contribute to regulate several cellular activities including differentiation, apoptosis, proliferation, and migration. The so-called "matricellular" proteins (MPs) have recently emerged as important regulators of ECM functions. The aim of our review is to consider all different types of MPs family assessing the potential relationship between MPs and survival in patients with pancreatic ductal adenocarcinoma (PDAC). A systematic computer-based search of published articles, according to the Preferred Reporting Items for Systematic reviews and Meta-Analysis (PRISMA) Statement issued in 2009 was conducted through Ovid interface, and literature review was performed in May 2017. The search text words were identified by means of controlled vocabulary, such as the National Library of Medicine's MESH (Medical Subject Headings) and Keywords. Collected data showed an important role of MPs in carcinogenesis and in PDAC prognosis even though the underlying mechanisms are still largely unknown and data are not univocal. Therefore, a better understanding of MPs role in regulation of ECM homeostasis and remodeling of specific organ niches may suggest potential novel extracellular targets for the development of efficacious therapeutic strategies.

Keywords: Cancer; Matricellular proteins; Pancreas; Pancreatic adenocarcinoma; Review.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Extracellular Matrix / genetics
  • Extracellular Matrix / metabolism*
  • Gene Expression Regulation, Neoplastic / physiology
  • Humans
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / pathology*
  • Survival Analysis