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Preclinical evidences toward the use of triterpenoid CDDO-Me for solid cancer prevention and treatment
Yan-Yang Wang1, Hong Zhe, Ren Zhao
1Department of Radiation Oncology, General Hospital of Ningxia Medical University, No,804 Shengli Str, Yinchuan, Ningxia, China. shsyztd@sohu.com.
Abstract:
Solid cancer remains a major cause of death in the world. As limited treatment options are currently available to patients with solid cancer, novel preventive control and effective therapeutic approaches are considered to be reasonable and decisive measures to combat this disease. The plant-derived triterpenoids, commonly used for medicinal purposes in many Asian countries, poses various pharmacological properties. A large number of triterpenoids exhibit cytotoxicity against a variety of cancer cells, and cancer preventive, as well as anticancer efficacy in preclinical animal models. To improve antitumor activity, some synthetic triterpenoid derivatives have been synthesized, including cyano-3,12-dioxooleana-1,9(11)- dien-28-oic (CDDO), its methyl ester (CDDO-Me), and imidazolide (CDDO-Im) derivatives. In this review, we will critically examine the current preclinical evidences of cancer preventive and therapeutic activity about one of the synthetic triterpenoids, CDDO-Me. Both in vitro and in vivo effects of this agent and related molecular mechanisms are presented.
Insights
Synthetic triterpenoid methyl ester (CDDO-Me) shows promising preclinical anticancer activity. This review examines its in vitro and in vivo effects and molecular mechanisms for solid cancer prevention and therapy.
Area of Science:
- Oncology
- Pharmacology
- Medicinal Chemistry
Background:
- Solid cancer is a leading global cause of mortality with limited therapeutic options.
- Plant-derived triterpenoids possess diverse pharmacological properties, including anticancer effects.
- Synthetic derivatives like CDDO-Me have been developed to enhance antitumor activity.
Purpose of the Study:
- To critically review preclinical evidence on the cancer-preventive and therapeutic activity of CDDO-Me.
- To present in vitro and in vivo effects of CDDO-Me.
- To elucidate the molecular mechanisms underlying CDDO-Me's anticancer actions.
Main Methods:
- Literature review of preclinical studies.
- Analysis of in vitro assays assessing cytotoxicity against cancer cells.
- Evaluation of in vivo studies in animal models for efficacy and safety.
Main Results:
- CDDO-Me exhibits significant cytotoxicity against various cancer cell lines.
- Preclinical animal models demonstrate cancer-preventive and therapeutic efficacy of CDDO-Me.
- Specific molecular pathways targeted by CDDO-Me are identified.
Conclusions:
- CDDO-Me represents a promising synthetic triterpenoid derivative for solid cancer treatment.
- Further research into its mechanisms and clinical potential is warranted.
- CDDO-Me could offer a novel therapeutic strategy for solid cancers.
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