Abstract
Objective To investigate the effect of mutant (T58A) and wild type ( WT) c-myc onp21Clpl and apoptosis of breast cancer cells in a p53-independent way. Methods Lentiviral vectors contai-ning c-myc T58A and WT were transfected into breast cancer cells HCC1937 ( cell transfection rate exceeds85% ) . Untreated cells ( group A) and cells transfected by lentivirus without c-myc gene (group B) servedas blank control group and transfection control group respectively. Cells stably expressing c-myc T58A(group C) and WT (group D) served as experiment groups. All the cells were then transfected by p21Cipi/siRNA. RT-PCR and Western blotting were used to detect the mRNA and protein levels of c-myc andp21Cipl,and the apoptosis was examined by using TdT-mediated dUTP nick end labeling (TUNEL) . Re-sults As compared with groups A and B,the c-myc was overexpressed in groups C and D ( all p 〈0. 01 ) . Before transfection, the p21c,pl in group C was highest (P 〈0. 01 ),while group D had the lowestexpression of p21Cipl (p 〈0. 01 ) ; the apoptosis rate in group C was lower than in other groups, and that ingroup D was the highest: (5. 5 ±0. 5)% , (5. 8 ±0. 3)% , (2. 8 ±0. 3)% and (9. 8 ±0. 8)% in groupsA,B,C and D, respectively (p 〈0.01). After transfection, the apoptosis rate in all groups were im-proved obviously (P 〈0.05). Conclusion Normally,in a non-p53 background,c-myc WT can suppressthe expression of p21c,pI,resulting in the increased apoptosis rate, but after mutation (T58A),the abilityof c-myc to induce apoptosis is decreased. Key words: Breast cancer; c-myc ; p21 cip1 ; Apoptosis
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