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10.1007/s11060-015-1905-z http://scihub22266oqcxt.onion/10.1007/s11060-015-1905-z C4612329!4612329 !26341370     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26341370 &cmd=llinks): Failed to open stream: HTTP request failed! 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Is CMV a target in pediatric glioblastoma? Expression of CMV proteins, pp65 and IE1-72 and CMV nucleic acids in a cohort of pediatric glioblastoma patients |pdf=|usr=}}{{26341370 }} gab.com Text Is CMV a target in pediatric glioblastoma Expression of CMV proteins, pp65 and IE1-72 and CMV nucleic acids in a cohort of pediatric glioblastoma patients JO: J Neurooncol http://www.kidney.de/pget.php?&tw=1&pmid=26341370 #FOAvip While the 5-year overall survival is better in pediatric than in adult patients diagnosed with glioblastoma (GBM), outcomes in children remain very poor. Understanding the mechanisms of tumorigenesis and tumor propagation can identify therapeutic targets to improve these outcomes. Human cytomegalovirus (CMV) proteins and nucleic acids are present in the majority of adult GBM. Indeed, CMV is emerging as a potential glioma-associated target for anti-CMV agents and cellular therapeutics. Furthermore, CMV appears to contribute to GBM's malignant phenotype, although its role in tumorigenesis is less certain. In this cohort of 25 serially diagnosed pediatric GBMs, the largest described cohort to date, we used immunohistochemical staining and in situ hybridization to show the presence of CMV antigens pp65 and IE1-72 as well as CMV nucleic acids, respectively. Our cohort indicated either CMV antigen pp65 or IE1-72 was present in approximately 67 % of pediatric GBM samples. The majority of samples stained positive for either CMV antigen showing a cytoplasmic pattern in 25-50 % of cells within the sample at a moderate intensity, while a few samples showed nuclear staining and higher grade/intensity. Of 16 samples where in situ hybridization was performed, 13 (81 %) showed specific staining using a CMV genome specific probe cocktail. ISH positive samples showed high concordance with being pp65 or IE1-72 positive. These findings, paired with the association of CMV expression with poor prognosis and overall survival, indicate the need to further investigate how these antigens are promoting tumor growth and preventing cell death. Also, the expression of these antigens in a majority of tumor tissues should be considered for immunotherapeutic targets in cases of pediatric GBM. Twit Text FOAVip Is CMV a target in pediatric glioblastoma Expression of CMV proteins, pp65 and IE1-72 and CMV nucleic acids in a cohort of pediatric glioblastoma patients ????J Neurooncol http://www.kidney.de/pget.php?&tw=1&pmid=26341370 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26341370 #FOAvip English Wikipedia <ref>{{Cite pmid|26341370 }}</ref> Is CMV a target in pediatric glioblastoma? Expression of CMV proteins, pp65 and IE1-72 and CMV nucleic acids in a cohort of pediatric glioblastoma patients #MMPMID26341370 Wakefield A ; Pignata A ; Ghazi A ; Ashoori A ; Hegde M ; Landi D ; Gray T ; Scheurer ME ; Chintagumpala M ; Adesina A ; Gottschalk S ; Hicks J ; Powell SZ ; Ahmed N J Neurooncol 2015[Nov]; 125 (2 ): 307-15 PMID26341370 show ga While the 5-year overall survival is better in pediatric than in adult patients diagnosed with glioblastoma (GBM), outcomes in children remain very poor. Understanding the mechanisms of tumorigenesis and tumor propagation can identify therapeutic targets to improve these outcomes. Human cytomegalovirus (CMV) proteins and nucleic acids are present in the majority of adult GBM. Indeed, CMV is emerging as a potential glioma-associated target for anti-CMV agents and cellular therapeutics. Furthermore, CMV appears to contribute to GBM's malignant phenotype, although its role in tumorigenesis is less certain. In this cohort of 25 serially diagnosed pediatric GBMs, the largest described cohort to date, we used immunohistochemical staining and in situ hybridization to show the presence of CMV antigens pp65 and IE1-72 as well as CMV nucleic acids, respectively. Our cohort indicated either CMV antigen pp65 or IE1-72 was present in approximately 67 % of pediatric GBM samples. The majority of samples stained positive for either CMV antigen showing a cytoplasmic pattern in 25-50 % of cells within the sample at a moderate intensity, while a few samples showed nuclear staining and higher grade/intensity. Of 16 samples where in situ hybridization was performed, 13 (81 %) showed specific staining using a CMV genome specific probe cocktail. ISH positive samples showed high concordance with being pp65 or IE1-72 positive. These findings, paired with the association of CMV expression with poor prognosis and overall survival, indicate the need to further investigate how these antigens are promoting tumor growth and preventing cell death. Also, the expression of these antigens in a majority of tumor tissues should be considered for immunotherapeutic targets in cases of pediatric GBM. |Adolescent [MESH] |Brain Neoplasms/*diagnosis/virology [MESH] |Child [MESH] |Child, Preschool [MESH] |Cohort Studies [MESH] |Cytomegalovirus/metabolism/pathogenicity [MESH] |Female [MESH] |Glioblastoma/*diagnosis/virology [MESH] |Humans [MESH] |Immediate-Early Proteins/*genetics/*metabolism [MESH] |Infant [MESH] |Male [MESH] |Phosphoproteins/*genetics/*metabolism [MESH]Is CMV a target in pediatric glioblastoma? Expression of CMV proteins,(epmc).pdf DeepDyve Pubget Overpricing