Inula viscosa (L.) Aiton Ethanolic Extract Inhibits the Growth of Human AGS and A549 Cancer Cell Lines

Author:

Rechek Habiba123,Haouat Ammar45,Hamaidia Kaouther16,Pinto Diana C. G. A.3ORCID,Boudiar Tarek7,Válega Mónica S. G. A.3,Pereira David M.8,Pereira Renato B.8,Silva Artur M. S.3

Affiliation:

1. Faculty of Sciences of Nature and Life Mohamed Cherif Messaadia University, Souk Ahras 41000 Souk-Ahras Algeria

2. Department of Biology of Organisms Faculty of Sciences of Nature and Life University of Batna 2 Mostefa Ben Boulaid 05078 Batna Algeria

3. LAQV-REQUIMTE & Department of Chemistry University of Aveiro 3810-193 Aveiro Portugal

4. Unité de Valorisation des Ressources Naturelles Molécules Bioactives et Analyse Physicochimiques et Biologiques (VARENBIOMOL) Université des Frères Mentouri 25000 Constantine Algeria

5. Department of Biology Faculty of Sciences of Nature and Life University of Oued Souf 39 000 Oued Souf Algeria

6. Laboratory of Applied Animal Biology Badji Mokhtar University 23000 Annaba Algeria

7. Center de Recherche en Biotechnologie Ali Mendjli Nouvelle Ville UV 03 BP E73 Constantine Algeria

8. REQUIMTE/LAQV Laboratório de Farmacognosia Departamento de Química Faculdade de Farmácia Universidade do Porto, R. Jorge Viterbo Ferreira n° 228 4050-313 Porto Portugal

Abstract

AbstractThe present study shows the chemical profile and cytotoxic properties of the ethanolic extracts of Inula viscosa from Northeast Algeria. The extract was obtained by maceration using ethanol. Its phenolic profile was determined using ultra‐high‐performance liquid chromatography coupled with a diode array detector and an electrospray mass spectrometer (UHPLC‐DAD‐ESI/MS), which allowed the identification and quantification of 17 compounds, 1,5‐O‐caffeoylquinic acid being the most abundant. The cytotoxic activity was assessed against human gastric cancer (AGS) and human non‐small‐cell lung cancer (A549) cell lines, whereas ethanolic extract elicited nearly 60 % and 40 % viability loss toward AGS and A549 cancer cells, respectively. Results also showed that cell death is caspase‐independent and confirmed the involvement of RIPK1 and the necroptosis pathway in the toxicity induced by the I. viscosa extract. In addition, the ethanolic extract would not provoke morphological traits in the cancer cells. These findings suggest that I. viscosa can be a source of new antiproliferative drugs or used in preparation plant‐derived pharmaceuticals.

Publisher

Wiley

Subject

Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering

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