» Articles » PMID: 30377589

Cytotoxic Activity of the Genus (Apiaceae) and Its Bioactive Constituents

Overview
Date 2018 Nov 1
PMID 30377589
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: The genus 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 are their cytotoxic effects. This article discusses cytotoxic activity of the genus 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 and their important compounds, the type of cell line used , concentrations of the extracts/active compound that were used, and the underlying mechanisms of action through which -related chemicals induced cytotoxicity. In addition, we explained different mechanisms of action through which the active constituents isolated from , could decrease cellular growth.

Conclusion: It is highly recommended that potent and effective compounds that were isolated from 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.

Citing Articles

Antiviral activity of on HSV-1, 2 .

Charostad J, Navidfar T, Kiani M, Schinitzler P, Astani A Iran J Microbiol. 2024; 16(6):786-791.

PMID: 39737349 PMC: 11682560. DOI: 10.18502/ijm.v16i6.17257.


Topical formulation of Boswellia nano emulsion in psoriasis mouse model.

Fereidouni M, Shadi M, Mahmoudian R, Ghasemi J, Mahzoon M, Faraji S Arch Dermatol Res. 2024; 317(1):144.

PMID: 39704841 DOI: 10.1007/s00403-024-03565-1.


Evaluation of the Potential Beneficial Effects of L. Extract Supplementation in Postmenopausal Discomfort.

Macri R, Maiuolo J, Scarano F, Musolino V, Fregola A, Gliozzi M Nutrients. 2024; 16(16).

PMID: 39203788 PMC: 11357168. DOI: 10.3390/nu16162651.


A Comprehensive Review of the Pharmacological Effects of Genus Ferula on Central Nervous System Disorders.

Bagheri S, Esmailidehaj M Cent Nerv Syst Agents Med Chem. 2024; 24(2):105-116.

PMID: 39034830 DOI: 10.2174/0118715249256485231031043722.


Cytotoxic and apoptotic effects of Ferula gummosa Boiss: extract on human breast adenocarcinoma cell line.

Rashidi R, Roohbakhsh A, Mohtashami L, Mobasheri L, Kheradmand H, Amiri M Mol Biol Rep. 2024; 51(1):592.

PMID: 38683376 DOI: 10.1007/s11033-024-09364-1.


References
1.
Gamal-Eldeen A, Hegazy M . A crystal lapiferin derived from Ferula vesceritensis induces apoptosis pathway in MCF-7 breast cancer cells. Nat Prod Res. 2010; 24(3):246-57. DOI: 10.1080/14786410802685398. View

2.
Safi R, Rodriguez F, Hilal G, Diab-Assaf M, Diab Y, El-Sabban M . Hemisynthesis, Antitumoral Effect, and Molecular Docking Studies of Ferutinin and Its Analogues. Chem Biol Drug Des. 2015; 87(3):382-97. DOI: 10.1111/cbdd.12670. View

3.
Shakeri A, Iranshahy M, Iranshahi M . Biological properties and molecular targets of umbelliprenin--a mini-review. J Asian Nat Prod Res. 2014; 16(8):884-9. DOI: 10.1080/10286020.2014.917630. View

4.
Alam M, Khan A, Wadood A, Khan A, Bashir S, Aman A . Bioassay-Guided Isolation of Sesquiterpene Coumarins from Ferula narthex Bioss: A New Anticancer Agent. Front Pharmacol. 2016; 7:26. PMC: 4754424. DOI: 10.3389/fphar.2016.00026. View

5.
Lee J, Choi S, Lee Y, Lee H, Kim K, Ahn K . Herbal compound farnesiferol C exerts antiangiogenic and antitumor activity and targets multiple aspects of VEGFR1 (Flt1) or VEGFR2 (Flk1) signaling cascades. Mol Cancer Ther. 2010; 9(2):389-99. DOI: 10.1158/1535-7163.MCT-09-0775. View