Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2002-4-17
pubmed:abstractText
Accumulating evidence suggests that lack of balance between proliferation and apoptosis may lead to clonal expansion and cancer emergence. In diffuse large B cell lymphoma (DLBCL), survivin expression by tumor cells has been recently described as a poor prognostic marker. We assessed the relationship between survivin gene up-regulation and several other factors involved in either cell cycle or apoptosis control. The expression of 34 genes from 27 cases of DLBCL with typical IPI factor-related poor prognostic outcome was analyzed by RNase protection assay. Using non-neoplastic tissues and low grade lymphomas as control, survivin expression was high in 80% of the cases without significant relation to patient overall survival (P = 0.64). However, the expression of several genes encoding for cell cycle inhibitors, cyclins, Bcl-2 or IAP family factors was significantly associated with the survivin up-regulation. Gene expression profiling showed that both survivin and cyclin B expression can define two subgroups of DLBCL: the previously described germinal center-like and activated B-like lymphomas, determined by protein expression analysis. We also identified a preferential survivin-cyclin B relationship (P = 0.017), suggesting that cyclin B over-expression, when linked to survivin over-expression in aggressive forms of lymphoma, might demonstrate a specific G2/M transition promotion.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/BIRC5 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Chromosomal Proteins, Non-Histone, http://linkedlifedata.com/resource/pubmed/chemical/Cyclin B, http://linkedlifedata.com/resource/pubmed/chemical/Cyclins, http://linkedlifedata.com/resource/pubmed/chemical/Inhibitor of Apoptosis Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Microtubule-Associated Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Neoplasm Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-bcl-2, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Neoplasm, http://linkedlifedata.com/resource/pubmed/chemical/Ribonuclease, Pancreatic
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0887-6924
pubmed:author
pubmed:issnType
Print
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
726-35
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:11960356-Adolescent, pubmed-meshheading:11960356-Adult, pubmed-meshheading:11960356-Aged, pubmed-meshheading:11960356-Aged, 80 and over, pubmed-meshheading:11960356-Apoptosis, pubmed-meshheading:11960356-Cell Cycle, pubmed-meshheading:11960356-Chromosomal Proteins, Non-Histone, pubmed-meshheading:11960356-Cyclin B, pubmed-meshheading:11960356-Cyclins, pubmed-meshheading:11960356-Female, pubmed-meshheading:11960356-Gene Expression, pubmed-meshheading:11960356-Gene Expression Profiling, pubmed-meshheading:11960356-Humans, pubmed-meshheading:11960356-Immunoenzyme Techniques, pubmed-meshheading:11960356-Inhibitor of Apoptosis Proteins, pubmed-meshheading:11960356-Lymphoma, Large B-Cell, Diffuse, pubmed-meshheading:11960356-Male, pubmed-meshheading:11960356-Microtubule-Associated Proteins, pubmed-meshheading:11960356-Middle Aged, pubmed-meshheading:11960356-Neoplasm Proteins, pubmed-meshheading:11960356-Proto-Oncogene Proteins c-bcl-2, pubmed-meshheading:11960356-RNA, Messenger, pubmed-meshheading:11960356-RNA, Neoplasm, pubmed-meshheading:11960356-Ribonuclease, Pancreatic
pubmed:year
2002
pubmed:articleTitle
Relationship between expression of genes involved in cell cycle control and apoptosis in diffuse large B cell lymphoma: a preferential survivin-cyclin B link.
pubmed:affiliation
Institut d'Etude et de Transfert de Gènes (IETG), Centre Hospitalier Régional et Universitaire, Hôpital Jean Minjoz, Besançon, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't