Triterpenoids and rexinoids as multifunctional agents for the prevention and treatment of cancer
Abstract
Synthetic oleanane triterpenoids and rexinoids are two new classes of multifunctional drugs. They are neither conventional cytotoxic agents, nor are they monofunctional drugs that uniquely target single steps in signal transduction pathways. Synthetic oleanane triterpenoids have profound effects on inflammation and the redox state of cells and tissues, as well as being potent anti-proliferative and pro-apoptotic agents. Rexinoids are ligands for the nuclear receptor transcription factors known as retinoid X receptors. Both classes of agents can prevent and treat cancer in experimental animals. These drugs have unique molecular and cellular mechanisms of action and might prove to be synergistic with standard anti-cancer treatments.
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Synthetic triterpenoids (TP), analogues of oleanolic acid, are powerful inhibitors of oxidative stress and cellular inflammatory processes, and thus may be neuroprotective in neurodegeneration.
“Synthetic triterpenoids (TP), analogues of oleanolic acid, are powerful inhibitors of oxidative stress and cellular inflammatory processes, and thus may be neuroprotective in neurodegeneration.”
From Mitochondrial Approaches for Neuroprotection (2008) · cites this paper as [181]
Synthetic TP compounds are potent inducers of the antioxidant response element (ARE)-Nrf2-Keap1 signaling pathway and are useful in a variety of cancers including leukemia, multiple myeloma, osteosarcoma, breast and lung cancer.
“Synthetic TP compounds are potent inducers of the antioxidant response element (ARE)–Nrf2–Keap1 signaling pathway and are useful in a variety of the cancers including leukemia, multiple myeloma, osteosarcoma, breast and lung cancer181.”
From Mitochondrial Approaches for Neuroprotection (2008) · cites this paper as [181]
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Self-citationBexarotene and Erlotinib for Aerodigestive Tract Cancer
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Self-citationIsopentenoids and Other Natural Products
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- Authors
- Liby, K. T., Yore, M. M., & Sporn, M. B.
- Affiliations
- Dartmouth College (US)
- Corresponding author
- Sporn, Michael B.
- ORCID
- Liby, Karen T.
- Venue
- Nature Reviews Cancer
- Published
- 2007-04-19
- Volume
- 7
- Issue
- 5
- Pages
- 357-369
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- OpenAlex
- W2000178617
- Cited by
- 637
- References
- 175
- Citations by year
- 2026: 9 · 2025: 13 · 2024: 23 · 2023: 30 · 2022: 32 · 2021: 23 · 2020: 28 · 2019: 27 · 2018: 15 · 2017: 35 · 2016: 36 · 2015: 44 · 2014: 47 · 2013: 43 · 2012: 48
- FWCI
- 3.46
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Cancer (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Natural product bioactivities and synthesis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Phytochemical Studies and Bioactivities
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacological Effects of Natural Compounds
- Keywords
- oleanane triterpenoids, rexinoids, cancer prevention, cancer therapy, retinoid X receptor, antiproliferative agents, apoptosis, inflammation, redox state, multi-target drugs, drug synergy
- MeSH terms
- Animals, Anti-Inflammatory Agents, Antineoplastic Agents, Dose-Response Relationship, Drug, Humans, Neoplasms, Oleanolic Acid, Anticarcinogenic Agents, Retinoid X Receptors, Mice
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