scispace - formally typeset
Open AccessJournal ArticleDOI

Pentacyclic triterpenes of the lupane, oleanane and ursane group as tools in cancer therapy.

Melanie N. Laszczyk
- 01 Dec 2009 - 
- Vol. 75, Iss: 15, pp 1549-1560
TLDR
This review summarizes the potential of triterpenes belonging to the lupane, oleanane or ursane group, to treat cancer by different modes of action and utilisation of different plants as their sources is of interest.
Abstract
Today cancer treatment is not only a question of eliminating cancer cells by induction of cell death. New therapeutic strategies also include targeting the tumour microenvironment, avoiding angiogenesis, modulating the immune response or the chronic inflammation that is often associated with cancer. Furthermore, the induction of redifferentiation of dedifferentiated cancer cells is an interesting aspect in developing new therapy strategies. Plants provide a broad spectrum of potential drug substances for cancer therapy with multifaceted effects and targets. Pentacyclic triterpenes are one group of promising secondary plant metabolites. This review summarizes the potential of triterpenes belonging to the lupane, oleanane or ursane group, to treat cancer by different modes of action. Since Pisha et al. reported in 1995 that betulinic acid is a highly promising anticancer drug after inducing apoptosis in melanoma cell lines in vitro and in vivo, experimental work focused on the apoptosis inducing mechanisms of betulinic acid and other triterpenes. The antitumour effects were subsequently confirmed in a series of cancer cell lines from other origins, for example breast, colon, lung and neuroblastoma. In addition, in the last decade many studies have shown further effects that justify the expectation that triterpenes are useful to treat cancer by several modes of action. Thus, triterpene acids are known mainly for their antiangiogenic effects as well as their differentiation inducing effects. In particular, lupane-type triterpenes, such as betulin, betulinic acid and lupeol, display anti-inflammatory activities which often accompany immune modulation. Triterpene acids as well as triterpene monoalcohols and diols also show an antioxidative potential. The pharmacological potential of triterpenes of the lupane, oleanane or ursane type for cancer treatment seems high; although up to now no clinical trial has been published using these triterpenes in cancer therapy. They provide a multitarget potential for coping with new cancer strategies. Whether this is an effective approach for cancer treatment has to be proven. Because various triterpenes are an increasingly promising group of plant metabolites, the utilisation of different plants as their sources is of interest. Parts of plants, for example birch bark, rosemary leaves, apple peel and mistletoe shoots are rich in triterpenes and provide different triterpene compositions.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Synthesis and evaluation of the anticancer activity of albiziabioside A and its analogues as apoptosis inducers against human melanoma cells

TL;DR: Albiziabioside A can induce cell cycle arrest in both the S and G2/M phases and induce A375 cell apoptosis via mitochondrial pathways involving a caspase cascade, providing for the first time a basic mechanism for the anticancer activity of 1.
Journal ArticleDOI

Triterpenoid Acids as Important Antiproliferative Constituents of European Elderberry Fruits

TL;DR: The phytochemical analysis revealed that ursolic and oleanolic acids are the main triterpenoids in the mentioned extract, which showed the highest activity in cancer cell lines compared to ethyl acetate extract, suggesting that nonpolar compounds are responsible for the cytotoxic activity.
Journal ArticleDOI

Recent Advances Regarding the Molecular Mechanisms of Triterpenic Acids: A Review (Part I)

TL;DR: The current review aims to summarize the most recent literature, published in the last five years, regarding the mechanism of action of three triterpenic acids (asiatic acid, oleanolic acid, and ursolic acid), corelated with different biological activities such as anticancer, anti-inflammatory, antidiabetic, cardioprotective, neuroprotective, hepatoprotective and antimicrobial.
Journal ArticleDOI

Targeting Mitochondrial Metabolism in Prostate Cancer with Triterpenoids.

TL;DR: In this article, the impact of triterpenoids on prostate cancer metabolism has been evaluated and a growing number of studies have assessed the impact on prostate metabolism, underlining their ability to hit different metabolic targets.
Journal ArticleDOI

Exploring Chemical and Biological Space of Terpenoids

TL;DR: This work has confirmed that terpenoid NPs have good drug-likeness and great potential for drug discovery, but more importantly, illuminated the uniqueness of cyclic scaffold diversity in different species and the specificity of biological function for the dominant fused-ring scaffolds of terpenoids.
References
More filters
Journal ArticleDOI

Free radicals and antioxidants in normal physiological functions and human disease

TL;DR: Attention is focussed on the ROS/RNS-linked pathogenesis of cancer, cardiovascular disease, atherosclerosis, hypertension, ischemia/reperfusion injury, diabetes mellitus, neurodegenerative diseases, rheumatoid arthritis, and ageing.
Journal ArticleDOI

Cancer-related inflammation.

TL;DR: The molecular pathways of this cancer-related inflammation are now being unravelled, resulting in the identification of new target molecules that could lead to improved diagnosis and treatment.
Journal ArticleDOI

Free radicals, metals and antioxidants in oxidative stress-induced cancer

TL;DR: This review examines the evidence for involvement of the oxidative stress in the carcinogenesis process and the role of enzymatic and non-enzymatic antioxidants in the process of carcinogenesis as well as the antioxidant interactions with various regulatory factors.
Journal ArticleDOI

Pharmacology of oleanolic acid and ursolic acid

TL;DR: Both oleanolic acid and ursolic acid are effective in protecting against chemically induced liver injury in laboratory animals and have been noted for their antitumor-promotion effects, which are stimulating additional research in this field.
Journal ArticleDOI

Discovery of betulinic acid as a selective inhibitor of human melanoma that functions by induction of apoptosis

TL;DR: As a result of bioassay–guided fractionation, betulinic acid, a pentacyclic triterpene, was identified as a melanoma–specific cytotoxic agent and antitumour activity was mediated by the induction of apoptosis.
Related Papers (5)