| Literature DB >> 10896772 |
J G Karras1, R A McKay, T Lu, J Pych, D A Frank, T L Rothstein, B P Monia.
Abstract
STAT3 is constitutively phosphorylated on tyrosine(705) in self-renewing, CD5(+) murine B-1 lymphocytes. Nuclear extracts from untreated primary B-1 or CD5(+) BCL(1) B lymphoma cells were found to contain immunoreactive STAT3 protein that binds to a sis-inducible element present in the promoter of the p21(waf1/cip1) tumor suppressor gene and is constitutively phosphorylated on serine(727). To determine the functional significance of constitutive STAT3 activation in B lymphoma cells, a specific STAT3 antisense oligonucleotide was developed and used to examine basal BCL(1) cell growth and IgM production. Abrogating STAT3 expression in BCL(1) cells inhibited their proliferative capacity and induced a corresponding decrease in secretion of IgM. Cell cycle analysis showed a block in progression through G1 in BCL(1) cells treated with the STAT3 antisense oligonucleotide. These results indicate that STAT3 controls cell growth and immunoglobulin secretion by enhancing progression through the G1 phase of the cell cycle in BCL(1) B cell lymphoma. Copyright 2000 Academic Press.Entities:
Mesh:
Substances:
Year: 2000 PMID: 10896772 DOI: 10.1006/cimm.2000.1661
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868