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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.

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Citations
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Journal ArticleDOI

1,2,3-triazole-substituted oleanolic Acid derivatives: synthesis and antiproliferative activity.

TL;DR: Some 18 new oleanolic acid derivatives were synthesized and the structures were confirmed by spectroscopic and spectrometric means and the antiproliferative activity of the new derivatives was evaluated towards normal lung fibroblasts, gastric epithelial adenocarcinoma, lung cancer, promyelocytic leukemia, and bladder carcinoma cells.
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Betulin as an antitumor agent tested in vitro on A431, HeLa and MCF7, and as an angiogenic inhibitor in vivo in the CAM assay.

TL;DR: In vitro results proved the superior specificity of betulin on cervical cancer cells, followed by skin cancer Cells, and the apoptotic mechanism, as well as the implication in the capillary formation of the chicken embryo chorioallantoic membrane.
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Maslinic acid derivatives induce significant apoptosis in b16f10 murine melanoma cells

TL;DR: Results indicate that maslinic acid derivatives are promising chemopreventive and chemotherapeutic agents.
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Ursolic and Oleanolic Acids: Plant Metabolites with Neuroprotective Potential.

TL;DR: In this article, the distribution of ursolic and oleanolic acids in plants, bioavailability and pharmacokinetic properties of these triterpenoids and their derivatives, and discuss their neuroprotective effects in vitro and in vivo.
Journal ArticleDOI

p53-p66shc/miR-21-Sod2 signaling is critical for the inhibitory effect of betulinic acid on hepatocellular carcinoma

TL;DR: It is demonstrated that p53 is responsible for the anti-tumor effect of BA through up-regulation of p66(shc) and miR-21 and down- regulation of Sod2 expression, leading to mitochondrial ROS accumulation and apoptosis.
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Journal ArticleDOI

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Journal ArticleDOI

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