HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Mitochondrial p53 phosphorylation induces Bak-mediated and caspase-independent cell death.

Abstract
Chemoresistance in cancer has previously been attributed to gene mutations or deficiency. Caspase mutations or Bax deficiency can lead to resistance to cancer drugs. We recently demonstrated that Bak initiates a caspase/Bax-independent cell death pathway. We show that Plumbagin (PL) (5-hydroxy-2-methyl-1,4-napthoquinone), a medicinal plant-derived naphthoquinone that is known to have anti-tumor activity in a variety of models, induces caspase-independent cell death in HCT116 Bax knockout (KO) or MCF-7 Bax knockdown (KD) cells that express wild-type (WT) Bak. The re-expression of Bax in HCT116 Bax KO cells fails to enhance the PL-induced cell death. Additionally, Bak knockdown by shRNA efficiently attenuates PL-induced cell death. These results suggest that PL-induced cell death depends primarily on Bak, not Bax, in these cells. Further experimentation demonstrated that p53 Ser15 phosphorylation and mitochondrial translocation mediated Bak activation and subsequent cell death. Knockdown of p53 or a p53 Ser15 mutant significantly inhibited p53 mitochondrial translocation and cell death. Furthermore, we found that Akt mediated p53 phosphorylation and the subsequent mitochondrial accumulation. Taken together, our data elaborate the role of Bak in caspase/Bax-independent cell death and suggest that PL may be an effective agent for overcoming chemoresistance in cancer cells with dysfunctional caspases.
AuthorsJinjing Wang, Wenhao Guo, Hang Zhou, Na Luo, Chunlai Nie, Xinyu Zhao, Zhu Yuan, Xinyu Liu, Yuquan Wei
JournalOncotarget (Oncotarget) Vol. 6 Issue 19 Pg. 17192-205 (Jul 10 2015) ISSN: 1949-2553 [Electronic] United States
PMID25980443 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents, Phytogenic
  • BAK1 protein, human
  • Naphthoquinones
  • RNA, Small Interfering
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • bcl-2 Homologous Antagonist-Killer Protein
  • bcl-2-Associated X Protein
  • Caspases
  • plumbagin
Topics
  • Antineoplastic Agents, Phytogenic (pharmacology)
  • Apoptosis (drug effects)
  • Blotting, Western
  • Caspases (metabolism)
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm (drug effects, physiology)
  • Fluorescent Antibody Technique
  • Gene Knockdown Techniques
  • Gene Knockout Techniques
  • Humans
  • Mitochondria (metabolism)
  • Naphthoquinones (pharmacology)
  • Phosphorylation
  • RNA, Small Interfering
  • Transfection
  • Tumor Suppressor Protein p53 (metabolism)
  • bcl-2 Homologous Antagonist-Killer Protein (metabolism)
  • bcl-2-Associated X Protein (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: