Anti-Inflammatory and Cytostatic Activities of a Parthenolide-Like Sesquiterpene Lactone fromCota palaestinasubsp.syriaca

Author:

Talhouk Rabih S.12,Nasr Bilal12,Fares Mohamed-Bilal13,Ajeeb Bushra24,Nahhas Rana2,Al Aaraj Lamis2,Talhouk Salma N.25ORCID,Ghaddar Tarek H.4,Saliba Najat A.24

Affiliation:

1. Department of Biology, Faculty of Arts and Sciences, American University of Beirut, Beirut 1107 2020, Lebanon

2. Nature Conservation Center (NCC), American University of Beirut, Beirut 1107 2020, Lebanon

3. Brain Mind Institute, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland

4. Department of Chemistry, Faculty of Arts and Sciences, American University of Beirut, Beirut 1107 2020, Lebanon

5. Landscape Design and Ecosystem Management, Faculty of Agriculture and Food Sciences, American University of Beirut, Beirut 1107 2020, Lebanon

Abstract

A sesquiterpene lactone 1-β,10-Epoxy-6-hydroxy-1,10H-inunolide (K100) was isolated through “bioassay-guided fractionation” fromCota palaestinasubsp.syriaca, an Eastern Mediterranean endemic plant. K100 inhibited endotoxin- (ET-) induced proinflammatory markers: IL-6, MMP-9, and NO in normal mouse mammary SCp2 Cells. Molecular dockingin silicosuggested that K100, having highly analogous structure as parthenolide (PTL), an anticancer compound, could bind PTL target proteins at similar positions and with comparable binding affinities. Both compounds, K100 and PTL, inhibited the proliferation and prolonged the S-phase of the cell cycle of breast adenocarcinoma MDA-MB-231 cells grown in 2D cultures. Noncytotoxic concentrations of K100 and PTL decreased the proliferation rate of MDA-MB-231 and shifted their morphology from stellate to spherical colonies in 3D cultures. This was accompanied with a significant increase in the amount of small colonies and a decrease in the amount of large colonies. Moreover, K100 and PTL decreased cellular motility and invasiveness of MDA-MB-231 cells. In summary, these results suggest that K100 exhibits PTL-analogous anti-inflammatory, cytostatic, and antimetastatic effects.

Funder

American University of Beirut

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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