Induction of apoptosis and cell cycle arrest by chloroform fraction of Juniperus phoenicea and chemical constituents analysis

Author:

Barnawi Ibrahim O.1,Nasr Fahd A.2,Noman Omar M.2,Alqahtani Ali S.23,Al-zharani Mohammed4,Alotaibi Amal A.5,Daradka Haytham M.1,Al-Mishari Abdullah A.2,Alobaid Waleed A3,Alqahtani Abdulaziz3,Herqash Rasheed N.2

Affiliation:

1. Department of Biological Sciences, College of Science, Taibah University , Al-Madinah Al- Munawwarah 41321 , Saudi Arabia

2. Department of Pharmacognosy, Medicinal, Aromatic and Poisonous Plants Research Center, College of Pharmacy, King Saud University , Riyadh 11451 , Saudi Arabia

3. Department of Pharmacognosy, College of Pharmacy, King Saud University , Riyadh 11451 , Saudi Arabia

4. Biology Department, College of Science, Imam Mohammad ibn Saud Islamic University (IMSIU) , Riyadh 11623 , Saudi Arabia

5. Basic Science Department, College of Medicine, Princess Nourah bint Abdulrahman University , Riyadh 11671 , Saudi Arabia

Abstract

Abstract Different phytochemicals from various plant species exhibit promising medicinal properties against cancer. Juniperus phoenicea is a plant species that has been found to present medicinal properties. Herein, crude extract and fractions of J. phoenicea were examined to determine its anticancer properties against several cancer cells. The active fraction was chosen to assess its activity on cell cycle progression and apoptosis induction by annexin and propidium iodide (PI) biomarkers. Further, phytochemical screening for possible contents of active fraction using gas chromatography–mass spectrometry (GC-MS) analysis was conducted. It was demonstrated that cell proliferation was suppressed, and the MCF-7 cell line was the most sensitive to J. phoenicea chloroform fraction (JPCF), with the IC50 values of 24.5 μg/mL. The anti-proliferation activity of JPCF in MCF-7 cells was linked to the aggregation of cells in the G1 phase, increases in early and late apoptosis as well as necrotic cell death. Contents analysis of JPCF using GC-MS analysis identified 3-methyl-5-(2′,6′,6′-trimethylcyclohex-1′-enyl)-1-penten-3-ol (16.5%), methyl 8-oxooctanoate (15.61%), cubenol (13.48%), and 7-oxabicyclo [2.2.1] heptane (12.14%) as major constituents. Our present study provides clear evidence that J. phoenicea can inhibit cell proliferation, trigger cell cycle arrest, and induce apoptosis in tested cancer cells.

Publisher

Walter de Gruyter GmbH

Subject

Materials Chemistry,General Chemistry

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