Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Jul-Aug;8(4):296-312.

Cytotoxic activity of the genus Ferula (Apiaceae) and its bioactive constituents

Affiliations
Review

Cytotoxic activity of the genus Ferula (Apiaceae) and its bioactive constituents

Mehrdad Iranshahi et al. Avicenna J Phytomed. 2018 Jul-Aug.

Abstract

Objective: The genus Ferula L. includes perennial flowering plants belonging to the Apiaceae family. This genus is a rich source of biologically active phytochemicals such as sulfur-containing derivatives, coumarins, sesquiterpenes, sesquiterpene lactones, sesquiterpene coumarins, glucuronic acid, galactose, arabinose, rhamnose, and daucane esters. Over the last decade, considerable attention has been paid to biological activities of these compounds; it is assumed that the most prominent biological features of the genus Ferula are their cytotoxic effects. This article discusses cytotoxic activity of the genus Ferula and their important compounds.

Materials and methods: In this mini-review article, papers published from 1990 to April 2016 were included and the following information was discussed; cytotoxic activity of the genus Ferula and their important compounds, the type of cell line used in vitro, concentrations of the extracts/active compound that were used, and the underlying mechanisms of action through which Ferula-related chemicals induced cytotoxicity. In addition, we explained different mechanisms of action through which the active constituents isolated from Ferula, could decrease cellular growth.

Conclusion: It is highly recommended that potent and effective compounds that were isolated from Ferula plants and found to be appropriate as adjuvant therapy for certain diseases, should be identified. Also, the versatile biological activities of sesquiterpene coumarins suggest them as promising agents with a broad range of biological applications to be used in the future.

Keywords: Apiaceae; Biological activity; Cytotoxicity; Farnesiferol C; Ferula; Sesquiterpene coumarin; Umbelliprenin.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure1
Figure1
Chemical structure of some constituents of Ferula categorized in groups A-E
Figure2
Figure2
Overview of different mechanisms through which Ferula-isolated compounds decrease cellular growth

Similar articles

Cited by

References

    1. Aas Z, Babaei E, Feizi MAH, Dehghan G. Anti-proliferative and apoptotic effects of dendrosomal farnesiferol c on gastric cancer cells. Asian Pac J Cancer Prev. 2015;16:5325–5329. - PubMed
    1. Alam M, Khan A, Wadood A, Khan A, Bashir S, Aman A, Jan AK, Rauf A, Ahmad B, Khan AR. Bioassay-guided isolation of sesquiterpene coumarins from Ferula narthex Bioss: A new anticancer agent. Front pharmacol. 2016;7:26–40. - PMC - PubMed
    1. Aldaghi L, Rad A, Arab A, Kasaian J, Iranshahi M, Sadr A, Soltani F. In silico and in vitro evaluation of cytotoxic activities of farnesiferol c and microlobin on MCF-7, HeLa and KYSE Cell Lines. Drug Res. 2016;66:532–538. - PubMed
    1. Altmann K-H, Gertsch J. Anticancer drugs from nature—natural products as a unique source of new microtubule-stabilizing agents. Nat Prod Rep. 2007;24:327–357. - PubMed
    1. Appendino G, Maxia L, Bascope M, Houghton PJ, Sanchez-Duffhues G, Muñoz E, Sterner O. A meroterpenoid NF-κB inhibitor and drimane sesquiterpenoids from asafetida. J Nat Prod. 2006;69:1101–1104. - PubMed

LinkOut - more resources