Matrix Effectors in the Pathogenesis of Keratinocyte-Derived Carcinomas.

collagen extracellular matrix hyaluronan metalloproteinases proteoglycans skin

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2022
Historique:
received: 19 02 2022
accepted: 11 04 2022
entrez: 16 5 2022
pubmed: 17 5 2022
medline: 17 5 2022
Statut: epublish

Résumé

Basal cell carcinoma (BCC) and cutaneous squamous cell carcinoma (cSCC), referred to as keratinocyte carcinomas, are skin cancer with the highest incidence. BCCs, rarely metastasize; whereas, though generally not characterized by high lethality, approximately 2-4% of primary cSCCs metastasize with patients exhibiting poor prognosis. The extracellular matrix (ECM) serves as a scaffold that provides structural and biological support to cells in all human tissues. The main components of the ECM, including fibrillar proteins, proteoglycans (PGs), glycosaminoglycans (GAGs), and adhesion proteins such as fibronectin, are secreted by the cells in a tissue-specific manner, critical for the proper function of each organ. The skin compartmentalization to the epidermis and dermis compartments is based on a basement membrane (BM), a highly specialized network of ECM proteins that separate and unify the two compartments. The stiffness and assembly of BM and tensile forces affect tumor progenitors' invasion at the stratified epithelium's stromal border. Likewise, the mechanical properties of the stroma, e.g., stiffness, are directly correlated to the pathogenesis of the keratinocyte carcinomas. Since the ECM is a pool for various growth factors, cytokines, and chemokines, its' intense remodeling in the aberrant cancer tissue milieu affects biological functions, such as angiogenesis, adhesion, proliferation, or cell motility by regulating specific signaling pathways. This review discusses the structural and functional modulations of the keratinocyte carcinoma microenvironment. Furthermore, we debate how ECM remodeling affects the pathogenesis of these skin cancers.

Identifiants

pubmed: 35572966
doi: 10.3389/fmed.2022.879500
pmc: PMC9100789
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

879500

Informations de copyright

Copyright © 2022 Kavasi, Neagu, Constantin, Munteanu, Surcel, Tsatsakis, Tzanakakis and Nikitovic.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Rafaela-Maria Kavasi (RM)

Laboratory of Histology-Embryology, Medical School, University of Crete, Heraklion, Greece.

Monica Neagu (M)

Immunology Laboratory, Victor Babes National Institute of Pathology, Bucharest, Romania.
Colentina Hospital, Bucharest, Romania.
Doctoral School, University of Bucharest, Bucharest, Romania.

Carolina Constantin (C)

Immunology Laboratory, Victor Babes National Institute of Pathology, Bucharest, Romania.
Colentina Hospital, Bucharest, Romania.
Doctoral School, University of Bucharest, Bucharest, Romania.

Adriana Munteanu (A)

Immunology Laboratory, Victor Babes National Institute of Pathology, Bucharest, Romania.
Doctoral School, University of Bucharest, Bucharest, Romania.

Mihaela Surcel (M)

Immunology Laboratory, Victor Babes National Institute of Pathology, Bucharest, Romania.

Aristidis Tsatsakis (A)

Forensic Science Department, Medical School, University of Crete, Heraklion, Greece.

George N Tzanakakis (GN)

Laboratory of Histology-Embryology, Medical School, University of Crete, Heraklion, Greece.

Dragana Nikitovic (D)

Laboratory of Histology-Embryology, Medical School, University of Crete, Heraklion, Greece.

Classifications MeSH