Under-expression of CK2β subunit in ccRCC represents a complementary biomarker of p-STAT3 Ser727 that correlates with patient survival

Clear cell renal cell carcinoma (ccRCC) is the most common and aggressive subtype of renal cancer. STAT3 pathway is altered in these tumors and p-STAT3 Ser727 is an independent prognostic factor for ccRCC. Protein kinase CK2 is altered in different types of tumors and overexpression of CK2α is consi...

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Detalles Bibliográficos
Autores: Vilardell, Jordi, Alcaraz Muñoz, Estefania, Sarró, Eduard|||0000-0001-7723-2916, Trilla Herrera, Enrique|||0000-0001-9401-0872, Cuadros, Thais|||0000-0001-6994-2424, Torres Ramírez, Inés Ma. de, Plana i Coll, Maria|||0000-0001-5808-9229, Ramón y Cajal, Santiago|||0000-0002-3867-1390, Pinna, Lorenzo A., Ruzzene, Maria, Morote Robles, Juan|||0000-0002-2168-323X, Meseguer Navarro, Anna|||0000-0003-3833-2249, Itarte, Emilio|||0000-0002-9366-5807
Tipo de recurso: artículo
Fecha de publicación:2018
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:187895
Acceso en línea:https://ddd.uab.cat/record/187895
https://dx.doi.org/urn:doi:10.18632/oncotarget.23422
Access Level:acceso abierto
Palabra clave:Protein kinase CK2
Clear cell renal cell carcinoma (ccRCC)
Epithelial-to-mesenchymal transition (EMT)
STAT3
Patient outcome
Descripción
Sumario:Clear cell renal cell carcinoma (ccRCC) is the most common and aggressive subtype of renal cancer. STAT3 pathway is altered in these tumors and p-STAT3 Ser727 is an independent prognostic factor for ccRCC. Protein kinase CK2 is altered in different types of tumors and overexpression of CK2α is considered predictive of bad prognosis and metastatic risk. CK2 subunits analyses in ccRCC samples showed increased CK2α/α' nuclear content in all cases, but decreased cytosolic CK2β (CK2βcyt) levels in the more advanced tumors. Stable downregulation of CK2β in renal proximal tubular (HK-2) and clear cell adenocarcinoma (786-O) cells triggered changes in E-cadherin, vimentin and Snail1 protein levels indicative of epithelial-to-mesenchymal transition (EMT), and increased HIF-α. Moreover, CK2β was required in order to observe STAT3 Ser727 phosphorylation in HK-2 but not in 786-O cells. We also observed that CK2β improved the prognostic value of p-STAT3 Ser727, as CK2βcyt.