Source:http://linkedlifedata.com/resource/pubmed/id/20446017
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0040649,
umls-concept:C0040661,
umls-concept:C0079744,
umls-concept:C0185117,
umls-concept:C0205225,
umls-concept:C0868928,
umls-concept:C0927232,
umls-concept:C0936012,
umls-concept:C1367307,
umls-concept:C1514923,
umls-concept:C1705162,
umls-concept:C1710082,
umls-concept:C2911684
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pubmed:issue |
2
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pubmed:dateCreated |
2010-11-18
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pubmed:abstractText |
Most primary central nervous system lymphomas (PCNSL) occurring in immunocompetent patients are diffuse large B-cell lymphomas (DLBCL), characterized by poor prognosis. An activated B-cell (ABC) origin of PCNSL has been postulated based on bcl-6 and MUM-1 expression by majority of these tumors. ABC DLBCL has been functionally subdivided using gene expression profiling and immunohistochemical analysis into STAT3-high and STAT-3 low subsets. A potentially crucial difference between STAT3-high and STAT3-low ABC DLBCL is in the expression of bcl-2 family members. STAT3-high cases are generally bcl-2 low and STAT3-low cases show higher expression of bcl-2. Further mechanisms such as activation of nuclear factor-kappa B (NF-?B) activation seem to be responsible for upregulation of bcl-2 in ABC subtype of DLBCL with an adverse outcome. As deregulation of STAT-3 pathway is known to play a critical role in ABC DLBCL and majority of the PCNSL are of the ABC subtype we studied the immunohistochemical expression of STAT-3 proteins in PCNSL along with other traditional markers (CD10, bcl-6, MUM-1 and bcl-2) in 17 cases of PCNSL occurring in immunocompetent patients. Despite lack of STAT3 expression in all our cases, majority (70%) of the patients with bcl-2 positive PCNSL had an adverse outcome similar to that reported in systemic lymphomas of ABC subtype. Based on our observations we propose that PCNSL represents a distinct subset of ABC diffuse large B-cell lymphomas with low STAT3 expression and perhaps mechanisms other than interaction of STAT-3 and NF-?B pathways may play a role in upregulation of bcl-2 in PCNSL. To the best of our knowledge expression of STAT-3 protein in PCNSL which represents a distinct anatomical subset of ABC DLBCL with a dismal prognosis has not been studied before.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1573-7373
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
100
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
249-53
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pubmed:meshHeading |
pubmed-meshheading:20446017-Aged,
pubmed-meshheading:20446017-Aged, 80 and over,
pubmed-meshheading:20446017-B-Lymphocytes,
pubmed-meshheading:20446017-Central Nervous System Neoplasms,
pubmed-meshheading:20446017-Female,
pubmed-meshheading:20446017-Humans,
pubmed-meshheading:20446017-Immunohistochemistry,
pubmed-meshheading:20446017-Immunophenotyping,
pubmed-meshheading:20446017-Lymphoma, Large B-Cell, Diffuse,
pubmed-meshheading:20446017-Male,
pubmed-meshheading:20446017-Middle Aged,
pubmed-meshheading:20446017-Prognosis,
pubmed-meshheading:20446017-Retrospective Studies,
pubmed-meshheading:20446017-STAT3 Transcription Factor,
pubmed-meshheading:20446017-Survival Analysis
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pubmed:year |
2010
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pubmed:articleTitle |
Expression of signal transducer and activator of transcription 3 (STAT3) in primary central nervous system diffuse large B-cell lymphoma: a retrospective analysis of 17 cases.
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pubmed:affiliation |
Division of Hematopathology, Department of Pathology, SUNY Upstate Medical University, Syracuse, NY, USA. vajpayen@upstate.edu
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pubmed:publicationType |
Journal Article
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