Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1998-8-6
pubmed:abstractText
The Fas receptor (APO-1/CD95) is capable of inducing apoptosis of lymphoid cells and is expressed in some non-Hodgkin's lymphomas (NHLs). Fas expression is up-regulated at the surface of normal B cells upon triggering of the CD40 receptor. In this report, we investigated the sensitivity of NHLs to Fas-mediated apoptosis induced by anti-Fas monoclonal antibodies (MAbs) and its possible modulation by CD40 ligation in 18 NHL biopsy samples of various histological subtypes. Flow cytometric analysis showed that the fraction of Fas-expressing lymphoma cells was highly variable from sample to sample (from 1% to 93%, mean value 46%). The frequency of apoptotic cells was not significantly increased upon treatment with an anti-Fas MAb compared with control MAb in the 18 NHL cases analysed. The sensitivity of lymphoma cells to Fas-mediated apoptosis was correlated neither with the histological subtypes nor with the level of Fas expression. Activation of neoplastic B cells by CD40 ligation resulted in significant increases in Fas expression and Fas-induced apoptosis among the five B-NHL cases tested. The overall increase in apoptotic rates was moderate and remained lower in tumour samples than in control CD40-activated normal tonsil B cells. Altogether, our results indicate that the sensitivity to Fas-induced apoptosis is null or weak in NHL cells, irrespective of their histological subtype, and that it can be increased to a moderate and variable degree by CD40 ligation on neoplastic B cells. This may be an impediment to the development of Fas-based therapies for NHLs.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-1372394, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-1375228, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-1498330, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-1689786, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-1713127, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-3924412, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7516669, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7520027, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7540067, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7545115, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7595197, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7595225, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7682455, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7684622, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7687619, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7889405, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-7917108, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8068936, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8207254, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8598453, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8616083, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8616718, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8624810, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8640839, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8642305, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8671627, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8695856, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8757604, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-8892631, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-9045928, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-9058704, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-9064331, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-9160689, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-9163608, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-9269827, http://linkedlifedata.com/resource/pubmed/commentcorrection/9683298-9531598
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0007-0920
pubmed:author
pubmed:issnType
Print
pubmed:volume
78
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
225-32
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1998
pubmed:articleTitle
Sensitivity to Fas-mediated apoptosis is null or weak in B-cell non-Hodgkin's lymphomas and is moderately increased by CD40 ligation.
pubmed:affiliation
Department of Hematopathology, Institut Paoli-Calmettes, Marseilles, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't