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  4. Identification of GRP75 as an independent favorable prognostic marker of neuroblastoma by a proteomics analysis
 
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Identification of GRP75 as an independent favorable prognostic marker of neuroblastoma by a proteomics analysis

Journal
Clinical Cancer Research
Journal Volume
14
Journal Issue
19
Pages
6237-6245
Date Issued
2008
Author(s)
WEN-MING HSU  
HSIN-YU LEE  
HSUEH-FEN JUAN  
Shih Y.-Y.
Wang B.-J.
CHIEN-YUAN PAN  
YUNG-MING JENG  
HSIU-HAO CHANG  
MENG-YAO LU  
Lin K.-H.
HONG-SHIEE LAI  
Chen W.-J.
Tsay Y.-G.
Liao Y.-F.
FON-JOU HSIEH  
DOI
10.1158/1078-0432.CCR-07-4181
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-58149157945&doi=10.1158%2f1078-0432.CCR-07-4181&partnerID=40&md5=ad07385e9e842634d89560d8f8d36e59
https://scholars.lib.ntu.edu.tw/handle/123456789/462446
Abstract
Purpose: Neuroblastoma (NB) is a heterogeneous neoplasm. Detailed biological discrimination is critical for the effective treatment of this disease. Because the tumor behavior of NB is closely associated with the histologic state of differentiation, we thus aimed to identify novel differentiation-associated markers of NB with prognostic implication. Experimental Design: A human NB cell line SH-SY5Y was used as a model system to explore potential biomarkers for the differentiation of NB by proteomic analyses. Seventy-two NB tumor tissues were subsequently investigated by immunohistochemistry to validate the correlations between the expression of a novel prognostic marker, various clinicopathologic and biological factors, and patient survival. Results: Using two-dimensional differential gel electrophoresis, we found a total of 24 spots of proteins in SH-SY5Y cells whose expression was enhanced following differentiation. Glucose-regulated protein 75 (GRP75) was unambiguously identified as one of the five proteins that were dramatically up-regulated following differentiation. Immunohistochemical analyses of 72 NB tumor tissues further revealed that positive GRP75 immunostaining is strongly correlated with differentiated histologies (P < 0.001), mass-screened tumors (P = 0.016), and early clinical stages (P < 0.001) but inversely correlated with MYCN amplification (P = 0.010). Univariate and multivariate survival analyses showed that GRP75 expressionis an independent favorable prognostic factor. Conclusions: The present findings clearly showed that our proteomics-based novel experimental paradigm could be a powerful tool to uncover novel biomarkers associated with the differentiation of NB. Our data also substantiate an essential role of GRP75 in the differentiation of NB. ?2008 American Association for Cancer Research.
SDGs

[SDGs]SDG3

Other Subjects
biological factor; glucose regulated protein; glucose regulated protein 75; tumor marker; unclassified drug; glucose regulated proteins; glucose-regulated proteins; heat shock protein 70; membrane protein; proteome; tumor marker; article; cancer staging; cancer survival; cell differentiation; cellular distribution; clinical feature; controlled study; histopathology; human; human cell; human tissue; immunohistochemistry; neuroblastoma; priority journal; prognosis; protein expression; protein synthesis; proteomics; two dimensional gel electrophoresis; child; female; gene expression regulation; infant; male; metabolism; methodology; neuroblastoma; newborn; preschool child; proteomics; tumor cell line; Cell Differentiation; Cell Line, Tumor; Child; Child, Preschool; Female; Gene Expression Regulation, Neoplastic; HSP70 Heat-Shock Proteins; Humans; Infant; Infant, Newborn; Male; Membrane Proteins; Neuroblastoma; Prognosis; Proteome; Proteomics; Tumor Markers, Biological
Type
journal article

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