CD133 Expression in Medullary Thyroid Cancer Cells Identifies Patients with Poor Prognosis

Abstract Context The identification of markers able to determine medullary thyroid cancer (MTC) patients at high-risk of disease progression is critical to improve their clinical management and outcome. Previous studies have suggested that expression of the stem cell marker CD133 is associated with...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 2020-11, Vol.105 (11), p.1-3561
Hauptverfasser: Cordero-Barreal, Alfonso, Caleiras, Eduardo, López de Maturana, Evangelina, Monteagudo, María, Martínez-Montes, Ángel M, Letón, Rocío, Gil, Eduardo, Álvarez-Escolá, Cristina, Regojo, Rita M, Andía, Víctor, Marazuela, Mónica, Guadalix, Sonsoles, Calatayud, María, Robles-Díaz, Luis, Aguirre, Miguel, Cano, Juana M, Díaz, José Ángel, Saavedra, Pilar, Lamas, Cristina, Azriel, Sharona, Sastre, Julia, Aller, Javier, Leandro-García, Luis J, Calsina, Bruna, Roldán-Romero, Juan María, Santos, María, Lanillos, Javier, Cascón, Alberto, Rodríguez-Antona, Cristina, Robledo, Mercedes, Montero-Conde, Cristina
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Sprache:eng
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Zusammenfassung:Abstract Context The identification of markers able to determine medullary thyroid cancer (MTC) patients at high-risk of disease progression is critical to improve their clinical management and outcome. Previous studies have suggested that expression of the stem cell marker CD133 is associated with MTC aggressiveness. Objective To evaluate CD133 impact on disease progression in MTC and explore the regulatory mechanisms leading to the upregulation of this protein in aggressive tumors. Patients We compiled a series of 74 MTCs with associated clinical data and characterized them for mutations in RET and RAS proto-oncogenes, presumed to be related with disease clinical behavior. Results We found that CD133 immunohistochemical expression was associated with adverse clinicopathological features and predicted a reduction in time to disease progression even when only RET-mutated cases were considered in the analysis (log-rank test P 
ISSN:0021-972X
1945-7197
DOI:10.1210/clinem/dgaa527