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BI1071, a Novel Nur77 Modulator, Induces Apoptosis of Cancer Cells by Activating the Nur77-Bcl-2 Apoptotic Pathway
Xiaohui Chen1, Xihua Cao2, Xuhuang Tu1
1School of Pharmaceutical Sciences, Fujian Provincial Key Laboratory of Innovative Drug Target Research, Xiamen University, Xiamen, China.
Abstract:
Nur77 (also called TR3 or NGFI-B), an orphan member of the nuclear receptor superfamily, induces apoptosis by translocating to mitochondria where it interacts with Bcl-2 to convert Bcl-2 from an antiapoptotic to a pro-apoptotic molecule. Nur77 posttranslational modification such as phosphorylation has been shown to induce Nur77 translocation from the nucleus to mitochondria. However, small molecules that can bind directly to Nur77 to trigger its mitochondrial localization and Bcl-2 interaction remain to be explored. Here, we report our identification and characterization of DIM-C-pPhCF3 +MeSO3 - (BI1071), an oxidized product derived from indole-3-carbinol metabolite, as a modulator of the Nur77-Bcl-2 apoptotic pathway. BI1071 binds Nur77 with high affinity, promotes Nur77 mitochondrial targeting and interaction with Bcl-2, and effectively induces apoptosis of cancer cells in a Nur77- and Bcl-2-dependent manner. Studies with animal model showed that BI1071 potently inhibited the growth of tumor cells in animals through its induction of apoptosis. Our results identify BI1071 as a novel Nur77-binding modulator of the Nur77-Bcl-2 apoptotic pathway, which may serve as a promising lead for treating cancers with overexpression of Bcl-2.
Insights
A novel compound, BI1071, targets the Nur77-Bcl-2 pathway to induce cancer cell apoptosis. This molecule promotes Nur77
Area of Science:
- Molecular Biology
- Cancer Research
- Pharmacology
Background:
- Nur77 (TR3/NGFI-B) is a nuclear receptor that induces apoptosis via mitochondrial translocation and interaction with Bcl-2.
- Nur77's apoptotic function is regulated by posttranslational modifications, but small molecule modulators are underexplored.
Purpose of the Study:
- To identify and characterize small molecules that modulate the Nur77-Bcl-2 apoptotic pathway.
- To investigate BI1071 as a potential therapeutic agent for cancer treatment.
Main Methods:
- High-affinity binding assays to assess Nur77 interaction.
- Mitochondrial translocation studies using cellular models.
- In vitro and in vivo cancer cell apoptosis assays.
- Animal model studies to evaluate tumor growth inhibition.
Main Results:
- BI1071, derived from an indole-3-carbinol metabolite, binds Nur77 with high affinity.
- BI1071 promotes Nur77 translocation to mitochondria and interaction with Bcl-2.
- BI1071 induces apoptosis in cancer cells in a Nur77- and Bcl-2-dependent manner.
- BI1071 effectively inhibits tumor growth in animal models.
Conclusions:
- BI1071 is a novel small molecule modulator of the Nur77-Bcl-2 apoptotic pathway.
- BI1071 demonstrates therapeutic potential for cancers overexpressing Bcl-2.
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