TY - JOUR
T1 - Chondroitin Sulfate Proteoglycan 4 as a Marker for Aggressive Squamous Cell Carcinoma
AU - Chen, K
AU - Yong, J
AU - Zauner, Roland
AU - Wally, Verena
AU - Whitelock, J
AU - Sajinovic, M
AU - Kopecki, Z
AU - Liang, K
AU - Scott, KF
AU - Mellick, AS
N1 - Zauner, Wally: EB House Austria, Research Program for Molecular Therapy of Genodermatoses, Department of Dermatology & Allergology, University Hospital of the Paracelsus Medical University, 5020 Salzburg, Austria
PY - 2022/11/13
Y1 - 2022/11/13
N2 - Chondroitin sulfate (CS) proteoglycan 4 (CSPG4) is a cell surface proteoglycan that is currently under investigation as a marker of cancer malignancy, and as a potential target of anticancer drug treatment. CSPG4 acts as a driver of tumourigenesis by regulating turnover of the extracellular matrix (ECM) to promote tumour cell invasion, migration as well as inflammation and angiogenesis. While CSPG4 has been widely studied in certain malignancies, such as melanoma, evidence is emerging from global gene expression studies, which suggests a role for CSPG4 in squamous cell carcinoma (SCC). While relatively treatable, lack of widely agreed upon diagnostic markers for SCCs is problematic, especially for clinicians managing certain patients, including those who are aged or infirm, as well as those with underlying conditions such as epidermolysis bullosa (EB), for which a delayed diagnosis is likely lethal. In this review, we have discussed the structure of CSPG4, and quantitatively analysed CSPG4 expression in the tissues and pathologies where it has been identified to determine the usefulness of CSPG4 expression as a diagnostic marker and therapeutic target in management of malignant SCC.
AB - Chondroitin sulfate (CS) proteoglycan 4 (CSPG4) is a cell surface proteoglycan that is currently under investigation as a marker of cancer malignancy, and as a potential target of anticancer drug treatment. CSPG4 acts as a driver of tumourigenesis by regulating turnover of the extracellular matrix (ECM) to promote tumour cell invasion, migration as well as inflammation and angiogenesis. While CSPG4 has been widely studied in certain malignancies, such as melanoma, evidence is emerging from global gene expression studies, which suggests a role for CSPG4 in squamous cell carcinoma (SCC). While relatively treatable, lack of widely agreed upon diagnostic markers for SCCs is problematic, especially for clinicians managing certain patients, including those who are aged or infirm, as well as those with underlying conditions such as epidermolysis bullosa (EB), for which a delayed diagnosis is likely lethal. In this review, we have discussed the structure of CSPG4, and quantitatively analysed CSPG4 expression in the tissues and pathologies where it has been identified to determine the usefulness of CSPG4 expression as a diagnostic marker and therapeutic target in management of malignant SCC.
KW - JUNCTIONAL EPIDERMOLYSIS-BULLOSA
KW - ANTIBODY-BASED IMMUNOTHERAPY
KW - MELANOMA-ASSOCIATED ANTIGEN
KW - PDGF ALPHA-RECEPTOR
KW - NG2 PROTEOGLYCAN
KW - PROGENITOR CELLS
KW - MOLECULAR-CLONING
KW - GROWTH-FACTOR
KW - MATRIX METALLOPROTEINASES
KW - PROMOTER METHYLATION
U2 - 10.3390/cancers14225564
DO - 10.3390/cancers14225564
M3 - Review article
C2 - 36428658
SN - 2072-6694
VL - 14
SP - 5564
JO - Cancers
JF - Cancers
IS - 22
ER -