Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2011-1-13
pubmed:abstractText
Low grade astrocytomas are the most common CNS tumors in neurofibromatosis type 1(NF1) patients. While most are classic pilocytic astrocytomas (PA), some are difficult to classify, and have been termed "low grade astrocytoma subtype indeterminate" (LGSI). Some of these tumors exhibit peculiar morphologies, including plump cytoplasmic processes and macronucleoli. In the current study we performed electron microscopy, followed by gene expression, immunohistochemicai and western blot analyses in an effort to identify biological differences underlying phenotypic variation in NF1-associated low grade astrocytoma. Electron microscopy demonstrated intermediate filaments and frequent Rosenthal fiber material in both PA and LGSI. Dense core granules and/or aligned microtubules were present in the LGSI group (2 of 3 cases) and in the PA group (1 of 10 cases). Analysis of global gene expression data obtained using Affymetrix HG-U133 Plus2.0 chips (5 PA, 1 LGSI), and western blot analysis for phospho-S6 (1 LGSI, 2 PA) demonstrated a gene expression profile reflecting "neuronal differentiation" and increased phospho-S6 immunoreactivity consistent with mTOR activation in the LGSI compared with PA. These findings were confirmed by immunohistochemistry for neuronal markers, as well as combined phospho-S6/ phospho-p70S6K immunoreactivity in 4 (of 4) LGSI vs. 5 (of 13) NF1-associated PA (p=0.02), and 13 (of 39) sporadic PA. Phospho-ERK immunoreactivity was uniformly present in PA and LGSI groups, while BRAF duplication was absent by FISH in 8 NF1-associated low grade astrocytomas. In summary, differential expression of neuronal-related genes and increased mTOR activation may underlie phenotypic variations in NF1-associated low grade astrocytomas.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-10358928, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-11575159, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-11914626, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-13764421, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-15337138, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-15624760, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-15805275, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-16453317, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-17175808, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-18344915, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-18974108, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-19017278, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-19018242, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-19371356, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-19713936, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-20600672, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-20697602, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-3318059, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-4474611, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-6767467, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-8928613, http://linkedlifedata.com/resource/pubmed/commentcorrection/21228927-9029763
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1936-2625
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
43-57
pubmed:dateRevised
2011-7-20
pubmed:meshHeading
pubmed-meshheading:21228927-Adolescent, pubmed-meshheading:21228927-Adult, pubmed-meshheading:21228927-Astrocytoma, pubmed-meshheading:21228927-Brain Neoplasms, pubmed-meshheading:21228927-Child, pubmed-meshheading:21228927-Child, Preschool, pubmed-meshheading:21228927-Comorbidity, pubmed-meshheading:21228927-DNA, Neoplasm, pubmed-meshheading:21228927-Female, pubmed-meshheading:21228927-Gene Expression Regulation, Neoplastic, pubmed-meshheading:21228927-Humans, pubmed-meshheading:21228927-In Situ Hybridization, Fluorescence, pubmed-meshheading:21228927-Male, pubmed-meshheading:21228927-Middle Aged, pubmed-meshheading:21228927-Neurofibromatosis 1, pubmed-meshheading:21228927-Neuroglia, pubmed-meshheading:21228927-Organelles, pubmed-meshheading:21228927-Phenotype, pubmed-meshheading:21228927-TOR Serine-Threonine Kinases, pubmed-meshheading:21228927-Young Adult
pubmed:year
2010
pubmed:articleTitle
Phenotypic variations in NF1-associated low grade astrocytomas: possible role for increased mTOR activation in a subset.
pubmed:affiliation
Departments of Laboratory Medicine and Pathology, Johns Hopkins University, Baltimore, MD, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural