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Chondroitin Sulfate Proteoglycan 4 as a Marker for Aggressive Squamous Cell Carcinoma

SIMPLE SUMMARY: Many solid tumours, such as those of the breast, colon, and prostate, have well established molecular markers of malignancy. However, in certain cancers, such as squamous cell carcinoma (SCC), few clinically useful biomarkers exist. Recently, several candidates that might be used for...

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Detalles Bibliográficos
Autores principales: Chen, Kathryn, Yong, Joel, Zauner, Roland, Wally, Verena, Whitelock, John, Sajinovic, Mila, Kopecki, Zlatko, Liang, Kang, Scott, Kieran Francis, Mellick, Albert Sleiman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688099/
https://www.ncbi.nlm.nih.gov/pubmed/36428658
http://dx.doi.org/10.3390/cancers14225564
Descripción
Sumario:SIMPLE SUMMARY: Many solid tumours, such as those of the breast, colon, and prostate, have well established molecular markers of malignancy. However, in certain cancers, such as squamous cell carcinoma (SCC), few clinically useful biomarkers exist. Recently, several candidates that might be used for diagnosis in SCC have been proposed. The purpose of this review is to discuss chondroitin sulfate (CS) proteoglycan 4 (CSPG4) as a tumour biomarker and explain why its expression might be considered in clinical decision making for patients with SCCs, including those of the head and neck, and those arising from rare genetic disorders, such as epidermolysis bullosa (EB). ABSTRACT: 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.