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PPAR Ligands Function as Suppressors That Target Biological Actions of HMGB1
Shibo Ying1, Xiang Xiao2, Tianhui Chen1
1Institute of Occupational Diseases, Zhejiang Academy of Medical Sciences, Hangzhou 310013, China.
Abstract:
High mobility group box 1 (HMGB1), which has become one of the most intriguing molecules in inflammatory disorders and cancers and with which ligand-activated peroxisome proliferator-activated receptors (PPARs) are highly associated, is considered as a therapeutic target. Of particular interest is the fact that certain PPAR ligands have demonstrated their potent anti-inflammatory activities and potential anticancer effects. In this review article we summarize recent experimental evidence that PPAR ligands function as suppressors that target biological actions of HMGB1, including intracellular expression, receptor signaling cascades, and extracellular secretion of HMGB1 in cell lines and/or animal models. We also propose the possible mechanisms underlying PPAR involvement in inflammatory disorders and discuss the future therapeutic value of PPAR ligands targeting HMGB1 molecule for cancer prevention and treatment.
Insights
Peroxisome proliferator-activated receptors (PPARs) ligands suppress high mobility group box 1 (HMGB1) actions, offering potential for treating inflammatory disorders and cancers. This review explores PPAR ligands as therapeutic targets for HMGB1-related diseases.
Area of Science:
- Molecular biology
- Immunology
- Oncology
Background:
- High mobility group box 1 (HMGB1) is implicated in inflammatory disorders and cancers.
- Ligand-activated peroxisome proliferator-activated receptors (PPARs) are closely associated with HMGB1.
- PPAR ligands exhibit anti-inflammatory and anticancer properties.
Purpose of the Study:
- To review evidence on PPAR ligands suppressing HMGB1 biological actions.
- To elucidate mechanisms of PPAR involvement in inflammation.
- To discuss the therapeutic potential of PPAR ligands targeting HMGB1 for cancer and inflammation.
Main Methods:
- Literature review of experimental evidence.
- Analysis of studies in cell lines and animal models.
- Exploration of molecular and signaling pathways.
Main Results:
- PPAR ligands inhibit HMGB1 intracellular expression.
- PPAR ligands interfere with HMGB1 receptor signaling.
- PPAR ligands reduce HMGB1 extracellular secretion.
Conclusions:
- PPAR ligands demonstrate suppressive effects on HMGB1.
- PPARs play a role in inflammatory disorders via HMGB1 modulation.
- Targeting HMGB1 with PPAR ligands holds promise for cancer prevention and treatment.
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