PUBLICATION
A novel strategy for glioblastoma treatment by induction of noptosis, an NQO1-dependent necrosis
- Authors
- Zhong, B., Yu, J., Hou, Y., Ai, N., Ge, W., Lu, J.J., Chen, X.
- ID
- ZDB-PUB-210220-13
- Date
- 2021
- Source
- Free radical biology & medicine 166: 104-115 (Journal)
- Registered Authors
- Keywords
- Glioblastoma, JNK1/2, NQO1, Noptosis, Tanshindiol B
- MeSH Terms
-
- Animals
- Apoptosis
- Cell Line, Tumor
- Glioblastoma*/drug therapy
- Glioblastoma*/genetics
- Humans
- Molecular Docking Simulation
- NAD(P)H Dehydrogenase (Quinone)/genetics
- Necrosis
- Zebrafish
- PubMed
- 33600944 Full text @ Free Radic. Biol. Med.
Citation
Zhong, B., Yu, J., Hou, Y., Ai, N., Ge, W., Lu, J.J., Chen, X. (2021) A novel strategy for glioblastoma treatment by induction of noptosis, an NQO1-dependent necrosis. Free radical biology & medicine. 166:104-115.
Abstract
Glioblastoma (GBM) is one of the most prevalent malignant primary tumors in the human brain. Temozolomide (TMZ), the chemotherapeutic drug for GBM treatment, induces apoptosis. Unfortunately, apoptosis-resistance to TMZ results in treatment failure. GBM shows enhanced expression of NAD(P)H: quinone oxidoreductase 1 (NQO1). Recently, noptosis, a type of NQO1-dependent necrosis, was proposed. Here, we identified that tanshindiol B (TSB) inhibits GBM growth by induction of noptosis. TSB triggered significant cell death, which did not fit the criteria of apoptosis but oxidative stress-induced necrosis. Molecular docking, cellular thermal shift assay, and NQO1 activity assay revealed that TSB bind to and promptly activated NQO1 enzyme activity. As the substrate of NQO1, TSB induced oxidative stress, which resulted in dramatic DNA damage, poly (ADP-ribose) polymerase 1 hyperactivation, and NAD+ depletion, leading to necrotic cell death. These effects of TSB were completely abolished by specific NQO1 inhibitor dicoumarol (DIC). Furthermore, the c-Jun N-terminal kinase (JNK1/2) plays an essential role in mediating TSB-induced cell death. Besides, TSB significantly suppressed tumor growth in a zebrafish xenograft model mediated by NQO1. In conclusion, these results showed that TSB was an NQO1 substrate and triggered noptosis of GBM. TSB exhibited anti-tumor potentials in GBM both in vitro and in vivo. This study provides a novel strategy for fighting GBM through the induction of noptosis.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping