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

被引:10
|
作者
Barnawi, Ibrahim O. [2 ]
Nasr, Fahd A. [1 ]
Noman, Omar M. [1 ]
Alqahtani, Ali S. [1 ,3 ]
Al-zharani, Mohammed [4 ]
Alotaibi, Amal A. [5 ]
Daradka, Haytham M. [2 ]
Al-Mishari, Abdullah A. [1 ]
Alobaid, Waleed A. [3 ]
Alqahtani, Abdulaziz [3 ]
Herqash, Rasheed N. [1 ]
机构
[1] King Saud Univ, Coll Pharm, Med Aromat & Poisonous Plants Res Ctr, Dept Pharmacognosy, Riyadh 11451, Saudi Arabia
[2] Taibah Univ, Coll Sci, Dept Biol Sci, Al Madinah Al Munawwarah 41321, Saudi Arabia
[3] King Saud Univ, Coll Pharm, Dept Pharmacognosy, Riyadh 11451, Saudi Arabia
[4] Imam Mohammad Ibn Saud Islamic Univ IMSIU, Coll Sci, Biol Dept, Riyadh 11623, Saudi Arabia
[5] Princess Nourah bint Abdulrahman Univ, Coll Med, Basic Sci Dept, Riyadh 11671, Saudi Arabia
来源
OPEN CHEMISTRY | 2021年 / 19卷 / 01期
关键词
Cupressaceae; Juniperus phoenicea; MTT assay; cancer; GC-MS; VITRO CYTOTOXIC ACTIVITY; CANCER; LEAVES; ANTIOXIDANT; DITERPENES; EXTRACTS; BERRIES; TARGETS;
D O I
10.1515/chem-2021-0195
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 mu g/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.
引用
收藏
页码:119 / 127
页数:9
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