Abstract 3657: MCM7, ADAM10, TRIM29, Aurora Kinase B, and Cyclin D1: A panel of prognostic protein markers for progression in non-muscle invasive bladder cancer - a multicenter tissue microarray validation study

Author(s):  
Niels Fristrup ◽  
Karin Birkenkamp-Demtröder ◽  
Benedicte Ulhøi ◽  
Francisco Mansilla ◽  
Marta Sanchez-Carbayo ◽  
...  
2013 ◽  
Vol 182 (2) ◽  
pp. 339-349 ◽  
Author(s):  
Niels Fristrup ◽  
Karin Birkenkamp-Demtröder ◽  
Thomas Reinert ◽  
Marta Sanchez-Carbayo ◽  
Ulrika Segersten ◽  
...  

2012 ◽  
Vol 180 (5) ◽  
pp. 1824-1834 ◽  
Author(s):  
Niels Fristrup ◽  
Benedicte P. Ulhøi ◽  
Karin Birkenkamp-Demtröder ◽  
Francisco Mansilla ◽  
Marta Sanchez-Carbayo ◽  
...  

2012 ◽  
Author(s):  
Niels Fristrup ◽  
Benedicte Parm Ulhøi ◽  
Karin Birkenkamp-Demtröder ◽  
Francisco Mansilla ◽  
Marta Sanchez-Carbayo ◽  
...  

2017 ◽  
Vol 72 (3) ◽  
pp. 461-469 ◽  
Author(s):  
Lars Dyrskjøt ◽  
Thomas Reinert ◽  
Ferran Algaba ◽  
Emil Christensen ◽  
Daan Nieboer ◽  
...  

Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2384
Author(s):  
Benito Blanco Gómez ◽  
Rubén López-Cortés ◽  
Francisco Javier Casas-Nebra ◽  
Sergio Vázquez-Estévez ◽  
Daniel Pérez-Fentes ◽  
...  

Because cystoscopy is expensive and invasive, a new method of detecting non-invasive muscular bladder cancer (NMIBC) is needed. This study aims to identify potential serum protein markers for NMIBC to improve diagnosis and to find treatment approaches that avoid disease progression to a life-threatening phenotype (muscle-invasive bladder cancer, MIBC). Here, silver nanoparticles (AgNPs, 9.73 ± 1.70 nm) as a scavenging device together with sequential window acquisition of all theoretical mass spectra (SWATH-MS) were used to quantitatively analyze the blood serum protein alterations in two NMIBC subtypes, T1 and Ta, and they were compared to normal samples (HC). NMIBC’s analysis of serum samples identified three major groups of proteins, the relative content of which is different from the HC content: proteins implicated in the complement and coagulation cascade pathways and apolipoproteins. In conclusion, many biomarker proteins were identified that merit further examination to validate their useful significance and utility within the clinical management of NMIBC patients.


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