c-Myc degradation induced by DNA damage results in apoptosis of CHO cells

Jiang MR, Li YC, Yang Y and Wu JR
Source: Oncogene
Publication Date: (2003)
Issue: 22: 3252-3259
Research Area:
Cancer Research/Cell Biology
UV41-CHO cells nucleofected with GFP tagged c-Myc and treated with TC showed a decreased amount of apoptotic cells, as scored by flow cytometry and counting of condensed nuclei. C-Myc degradation as a result of DNA damage is proposed to induce apoptosis.
Although tripchlorolide (TC), a compound purified from a Chinese herb Tripterygium Wilfordii Hook, has been demonstrated to be a potent antitumor agent, its mechanisms of action are unknown. The present study shows that TC induces apoptosis of Chinese Hamster Ovary (CHO) cells. Most strikingly, TC was particularly potent in inducing apoptosis of the UV41 mutant CHO cells, which are deficient in the ERCC4 gene encoding a nucleotide excision repair protein. TC caused a higher level of DNA damage in UV41 cells than those in the wild-type CHO cells or EM9 cells, which are deficient in single-strand break repair. These results provided a critical link between apoptotic hypersensitivity and DNA damage in defective nucleotide excision repair pathway of UV41 cells by TC treatment. Further analysis showed that degradation of the c-Myc protein in TC-treated UV41 cells was much stronger than those in the wild-type CHOAA8 and the EM9. A proteasome inhibitor, MG132, reduced both the degradation of c-Myc and apoptosis in TC-treated UV41 cells. Expression of exogenous c-Myc also inhibited apoptosis of TC-treated UV41 cells. These results indicate that c-Myc degradation induced by DNA damage in the presence of TC contributes to induction of apoptosis of UV41 cells.