Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Language
Year range
1.
Chinese Journal of Hematology ; (12): 640-643, 2003.
Article in Chinese | WPRIM | ID: wpr-354811

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the expression changes of intrinsic cytokines TGF-beta(1) and TNF-alpha, telomerase activity and bcl-2 during ongoing apoptosis of HL-60 and K562 cells induced by p53.</p><p><b>METHODS</b>pN53cG (Val135), a temperature sensitive p53 mutant, which behaved like wild type p53 (wt-p53) at 32.5 degrees C, were introduced into p53-null HL-60 and K562 cells respectively by lipofectin. In the presence of G418, HL-60-pN53cG and K562 pN53cG clones expressing p53 protein were selected. The ongoing expression of intrinsic cytokines (TGF-beta(1) and TNF-alpha), bcl-2 oncogene and hTERT mRNA during the apoptosis of HL-60 and K562 cells induced by p53 and the effects of exogenous p53 gene, TGF-beta(1) and TNF-alpha antisense PS-ODNS on the apoptosis of HL-60 and K562 cells and the expression of bcl-2 were studied by RT-PCR, quantitative RT-PCR, DNA fragmentation, TdT-mediated dUTP nick end labeling (TUNEL) and flow cytometery. The levels of secreted TGF-beta(1) and telomerase activity were detected by ELISA and PCR-ELISA, respectively.</p><p><b>RESULTS</b>(1) The expressions of intrinsic TGF-beta(1) and TNF-alpha mRNA were up-regulated, while that of bcl-2 and hTERT down-regulated. The levels of TGF-beta(1) in the supernatant of HL-60 and K562 cells were increased, and the level of telomerase activity decreased. (2) Antisense PS-ODNS of TGF-beta(1) and TNF-alpha could obviously inhibit the p53 inducing cell apoptosis, and restore bcl-2 mRNA and protein to pre-treated level.</p><p><b>CONCLUSIONS</b>Exogenous p53 induces leukemia cell apoptosis via up-regulating the expression of intrinsic TGF-beta(1) and TNF-alpha and down-regulating the expression of hTERT and bcl-2.</p>


Subject(s)
Humans , Apoptosis , Genetics , DNA, Antisense , Pharmacology , DNA-Binding Proteins , Gene Expression Regulation, Neoplastic , HL-60 Cells , K562 Cells , Leukemia , Genetics , Pathology , Mutation , Plasmids , Genetics , Proto-Oncogene Proteins c-bcl-2 , Genetics , RNA, Messenger , Genetics , Metabolism , Reverse Transcriptase Polymerase Chain Reaction , Telomerase , Genetics , Transfection , Methods , Transforming Growth Factor beta , Genetics , Transforming Growth Factor beta1 , Tumor Necrosis Factor-alpha , Genetics , Tumor Suppressor Protein p53 , Genetics , Physiology
SELECTION OF CITATIONS
SEARCH DETAIL