TY - JOUR
T1 - Proteomic studies on low- and high-grade human brain astrocytomas
AU - Odreman, Federico
AU - Vindigni, Marco
AU - Gonzales, Marlen Lujardo
AU - Niccolini, Benedetta
AU - Candiano, Giovanni
AU - Zanotti, Bruno
AU - Skrap, Miran
AU - Pizzolitto, Stefano
AU - Stanta, Giorgio
AU - Vindigni, Alessandro
PY - 2005/5
Y1 - 2005/5
N2 - Human brain astrocytomas range from the indolent low-grade to the highly infiltrating and aggressive high-grade form, also known as glioblastoma multiforme. The extensive heterogeneity of astrocytic tumors complicates their pathological classification. In this study, we compared the protein pattern of low-grade fibrillary astrocytomas to that of glioblastoma multiforme by 2D electrophoresis. The level of most proteins remains unchanged between the different grade tumors and only few differences are reproducibly observable. Fifteen differentially expressed proteins, as well as seventy conserved spots, were identified by mass spectrometry. Western and immnunohistochemical analysis confirmed the differential expression of the identified proteins. These data provide an initial reference map for brain gliomas. Among the proteins more highly expressed in glioblastoma multiforme, we found peroxiredoxin 1 and 6, the transcription factor BTF3, and α-B-crystallin, whereas protein disulfide isomerase A3, the catalytic subunit of the cAMP-dependent protein kinase, and the glial fibrillary acidic protein are increased in low-grade astrocytomas. Our findings contribute to deepening our knowledge of the factors that characterize this class of tumors and, at the same time, can be applied toward the development of novel molecular biomakers potentially useful for an accurate classification of the grade of astrocytomas.
AB - Human brain astrocytomas range from the indolent low-grade to the highly infiltrating and aggressive high-grade form, also known as glioblastoma multiforme. The extensive heterogeneity of astrocytic tumors complicates their pathological classification. In this study, we compared the protein pattern of low-grade fibrillary astrocytomas to that of glioblastoma multiforme by 2D electrophoresis. The level of most proteins remains unchanged between the different grade tumors and only few differences are reproducibly observable. Fifteen differentially expressed proteins, as well as seventy conserved spots, were identified by mass spectrometry. Western and immnunohistochemical analysis confirmed the differential expression of the identified proteins. These data provide an initial reference map for brain gliomas. Among the proteins more highly expressed in glioblastoma multiforme, we found peroxiredoxin 1 and 6, the transcription factor BTF3, and α-B-crystallin, whereas protein disulfide isomerase A3, the catalytic subunit of the cAMP-dependent protein kinase, and the glial fibrillary acidic protein are increased in low-grade astrocytomas. Our findings contribute to deepening our knowledge of the factors that characterize this class of tumors and, at the same time, can be applied toward the development of novel molecular biomakers potentially useful for an accurate classification of the grade of astrocytomas.
KW - 2D-gel electrophoresis
KW - Astrocytomas
KW - Gliomas
KW - Mass spectrometry
KW - Proteomics
UR - http://www.scopus.com/inward/record.url?scp=20844447307&partnerID=8YFLogxK
U2 - 10.1021/pr0498180
DO - 10.1021/pr0498180
M3 - Article
C2 - 15952716
AN - SCOPUS:20844447307
SN - 1535-3893
VL - 4
SP - 698
EP - 708
JO - Journal of Proteome Research
JF - Journal of Proteome Research
IS - 3
ER -