Literature DB >> 19742422

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

Melanie N Laszczyk1.   

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. Georg Thieme Verlag KG Stuttgart. New York.

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Year:  2009        PMID: 19742422     DOI: 10.1055/s-0029-1186102

Source DB:  PubMed          Journal:  Planta Med        ISSN: 0032-0943            Impact factor:   3.352


  104 in total

1.  Oleanane triterpenoids in the prevention and therapy of breast cancer: current evidence and future perspectives.

Authors:  Nisha R Parikh; Animesh Mandal; Deepak Bhatia; Kodappully Sivaraman Siveen; Gautam Sethi; Anupam Bishayee
Journal:  Phytochem Rev       Date:  2014-12       Impact factor: 5.374

2.  Triterpenoid resinous metabolites from the genus Boswellia: pharmacological activities and potential species-identifying properties.

Authors:  Yuxin Zhang; Zhangchi Ning; Cheng Lu; Siyu Zhao; Jianfen Wang; Baoqin Liu; Xuegong Xu; Yuanyan Liu
Journal:  Chem Cent J       Date:  2013-09-12       Impact factor: 4.215

3.  New ursane triterpenoids from Ficus pandurata and their binding affinity for human cannabinoid and opioid receptors.

Authors:  Amgad I M Khedr; Sabrin R M Ibrahim; Gamal A Mohamed; Hany E A Ahmed; Amany S Ahmad; Mahmoud A Ramadan; Atef E Abd El-Baky; Koji Yamada; Samir A Ross
Journal:  Arch Pharm Res       Date:  2016-06-27       Impact factor: 4.946

4.  Activity-guided purification identifies lupeol, a pentacyclic triterpene, as a therapeutic agent multiple pathogenic factors of acne.

Authors:  Hyuck Hoon Kwon; Ji Young Yoon; Seon Yong Park; Seonguk Min; Yong-Il Kim; Ji Yong Park; Yun-Sang Lee; Diane M Thiboutot; Dae Hun Suh
Journal:  J Invest Dermatol       Date:  2015-02-03       Impact factor: 8.551

Review 5.  Pharmacological modulation of mitochondrial ion channels.

Authors:  Luigi Leanza; Vanessa Checchetto; Lucia Biasutto; Andrea Rossa; Roberto Costa; Magdalena Bachmann; Mario Zoratti; Ildiko Szabo
Journal:  Br J Pharmacol       Date:  2019-01-02       Impact factor: 8.739

6.  Efficient synthesis and biological evaluation of epiceanothic acid and related compounds.

Authors:  Pu Zhang; Li Xu; Keduo Qian; Jun Liu; Luyong Zhang; Kuo-Hsiung Lee; Hongbin Sun
Journal:  Bioorg Med Chem Lett       Date:  2010-11-05       Impact factor: 2.823

7.  Terpenoids as potential chemopreventive and therapeutic agents in liver cancer.

Authors:  Roslin J Thoppil; Anupam Bishayee
Journal:  World J Hepatol       Date:  2011-09-27

8.  Phase I study of the synthetic triterpenoid, 2-cyano-3, 12-dioxoolean-1, 9-dien-28-oic acid (CDDO), in advanced solid tumors.

Authors:  Giovanna Speranza; Martin E Gutierrez; Shivaani Kummar; John M Strong; Robert J Parker; Jerry Collins; Yunkai Yu; Liang Cao; Anthony J Murgo; James H Doroshow; Alice Chen
Journal:  Cancer Chemother Pharmacol       Date:  2011-07-31       Impact factor: 3.333

9.  Disuccinyl betulin triggers metacaspase-dependent endonuclease G-mediated cell death in unicellular protozoan parasite Leishmania donovani.

Authors:  Sayan Chowdhury; Tulika Mukherjee; Somenath Roy Chowdhury; Souvik Sengupta; Sibabrata Mukhopadhyay; Parasuraman Jaisankar; Hemanta K Majumder
Journal:  Antimicrob Agents Chemother       Date:  2014-01-27       Impact factor: 5.191

10.  Molecular mechanisms of in vitro betulin-induced apoptosis of Leishmania donovani.

Authors:  Prakash Saudagar; Vikash Kumar Dubey
Journal:  Am J Trop Med Hyg       Date:  2014-01-13       Impact factor: 2.345

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