TY - JOUR
T1 - Extracellular Matrix Proteome Remodeling in Human Glioblastoma and Medulloblastoma
AU - Trombetta-Lima, Marina
AU - Rosa-Fernandes, Livia
AU - Angeli, Claudia B.
AU - Moretti, Isabele F.
AU - Franco, Yollanda M.
AU - Mousessian, Adaliana S.
AU - Wakamatsu, Alda
AU - Lerario, Antonio M.
AU - Oba-Shinjo, Sueli M.
AU - Pasqualucci, Carlos A.
AU - Marie, Suely K.N.
AU - Palmisano, Giuseppe
N1 - Funding Information:
This study would not be possible without the valuable assistance of the doctors and residents from the Discipline of Neurosurgery of the Department of Neurology at Hospital das Clinicas of School of Medicine, University of São Paulo in tumor sample collection. We are grateful for the financial support provided by the São Paulo Research Foundation [FAPESP, grants processes no 2014/06863-3 (G.P.), 2018/18257-1 (G.P.), 2018/15549-1 (G.P.), 2001/12898-4 (S.K.N.M.), 2004/12133-6 (S.K.N.M.), 2013/02162-8 (S.K.N.M.), 2014/50137-5 (S.K.N.M.), 2020/02988-7 (S.K.N.M. and S.M.O.-S.), 2015/26328-8 (M.T.L.), and 2016/14695-9 (I.F.M.)]; by the Conselho Nacional de Desenvolvimento Científico e Tecnológico [CNPq, grant no 305730/2015-0 (S.K.N.M.), “Bolsa de Produtividade” (S.K.N.M. and G.P.)]; by FMUSP (S.K.N.M. and S.M.O.-S.); and by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior [CAPES, grant no NUFFIC 062/15 (S.K.N.M.), processes no 9999.001625/2015-02 (S.K.N.M.), 88887.321693/2019-00 (M.T.L.), and 88887.351607/2019-00 (I.F.M.)].
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - Medulloblastomas (MBs) and glioblastomas (GBMs) are high-incidence central nervous system tumors. Different origin sites and changes in the tissue microenvironment have been associated with the onset and progression. Here, we describe differences between the extracellular matrix (ECM) signatures of these tumors. We compared the proteomic profiles of MB and GBM decellularized tumor samples between each other and their normal decellularized brain site counterparts. Our analysis revealed that 19, 28, and 11 ECM proteins were differentially expressed in MBs, GBMs, and in both MBs and GBMs, respectively. Next, we validated key findings by using a protein tissue array with 53 MB and 55 GBM cases and evaluated the clinical relevance of the identified differentially expressed proteins through their analysis on publicly available datasets, 763 MB samples from the GSE50161 and GSE85217 studies, and 115 GBM samples from RNAseq-TCGA. We report a shift toward a denser fibrillary ECM as well as a clear alteration in the glycoprotein signature, which influences the tumor pathophysiology. MS data have been submitted to the PRIDE repository, project accession: PXD023350.
AB - Medulloblastomas (MBs) and glioblastomas (GBMs) are high-incidence central nervous system tumors. Different origin sites and changes in the tissue microenvironment have been associated with the onset and progression. Here, we describe differences between the extracellular matrix (ECM) signatures of these tumors. We compared the proteomic profiles of MB and GBM decellularized tumor samples between each other and their normal decellularized brain site counterparts. Our analysis revealed that 19, 28, and 11 ECM proteins were differentially expressed in MBs, GBMs, and in both MBs and GBMs, respectively. Next, we validated key findings by using a protein tissue array with 53 MB and 55 GBM cases and evaluated the clinical relevance of the identified differentially expressed proteins through their analysis on publicly available datasets, 763 MB samples from the GSE50161 and GSE85217 studies, and 115 GBM samples from RNAseq-TCGA. We report a shift toward a denser fibrillary ECM as well as a clear alteration in the glycoprotein signature, which influences the tumor pathophysiology. MS data have been submitted to the PRIDE repository, project accession: PXD023350.
KW - decellularization
KW - extracellular matrix
KW - glioblastoma
KW - mass spectrometry
KW - medulloblastoma
KW - proteome
UR - http://www.scopus.com/inward/record.url?scp=85116165628&partnerID=8YFLogxK
U2 - 10.1021/acs.jproteome.1c00251
DO - 10.1021/acs.jproteome.1c00251
M3 - Article
C2 - 34533964
AN - SCOPUS:85116165628
SN - 1535-3893
VL - 20
SP - 4693
EP - 4707
JO - Journal of Proteome Research
JF - Journal of Proteome Research
IS - 10
ER -