ALCAM/CD166: A pleiotropic mediator of cell adhesion, stemness and cancer progression.
ALCAM/CD166
Cancer stem cell marker
Shedding
Structure
Tumor progression
Journal
Cytokine & growth factor reviews
ISSN: 1879-0305
Titre abrégé: Cytokine Growth Factor Rev
Pays: England
ID NLM: 9612306
Informations de publication
Date de publication:
10 2021
10 2021
Historique:
received:
17
06
2021
accepted:
05
07
2021
pubmed:
18
7
2021
medline:
16
10
2021
entrez:
17
7
2021
Statut:
ppublish
Résumé
Activated Leukocyte Cell Adhesion Molecule (ALCAM/CD166) is a glycoprotein involved in homotypic and heterotypic cell adhesion. ALCAM can be proteolytically cleaved at the cell surface by metalloproteases, which generate shedding of its ectodomain. In various tumors, ALCAM is overexpressed and serves as a valuable prognostic marker of disease progression. Moreover, CD166 has been identified as a putative cancer stem cell marker in particular cancers. Herein, we summarize biochemical aspects of ALCAM, including structure, proteolytic shedding, alternative splicing, and specific ligands, and integrate this information with biological functions of this glycoprotein including cell adhesion, migration and invasion. In addition, we discuss different patterns of ALCAM expression in distinct tumor types and its contribution to tumor progression. Finally, we highlight the role of ALCAM as a cancer stem cell marker and introduce current clinical trials associated with this molecule. Future studies are needed to define the value of shed ALCAM in biofluids or ALCAM isoform expression as prognostic biomarkers in tumor progression.
Identifiants
pubmed: 34272152
pii: S1359-6101(21)00055-1
doi: 10.1016/j.cytogfr.2021.07.001
pii:
doi:
Substances chimiques
ALCAM protein, human
0
Activated-Leukocyte Cell Adhesion Molecule
0
Antigens, CD
0
Biomarkers, Tumor
0
Cell Adhesion Molecules, Neuronal
0
Fetal Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
27-37Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.