Chamomile Essential Oil: Chemical Constituents and Antitumor Activity in MDA-MB-231 Cells through PI3K/Akt/mTOR Signaling Pathway

被引:8
|
作者
An, Zhonghua [1 ]
Feng, Xuelin [1 ]
Sun, Mengjia [1 ]
Wang, Yifan [1 ]
Wang, Hongbo [2 ]
Gong, Yanling [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem Engn, Dept Pharm, 53 Zhengzhou Rd, Qingdao 266042, Shandong, Peoples R China
[2] Jimo Dist Peoples Hosp, Dept Gastrointestinal Surg, 38 Jianmin St, Qingdao 266042, Shandong, Peoples R China
关键词
chamomile essential oil; GC; MS; TNBC; MDA-MB-231; PI3K; Akt; mTOR; MATRICARIA-RECUTITA L; BREAST-CANCER; CADINENE SESQUITERPENES; ANTIMICROBIAL ACTIVITY; BETA-CARYOPHYLLENE; ANTIOXIDANT; EXTRACT;
D O I
10.1002/cbdv.202200523
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chamomile essential oil (CEO) is extracted from chamomile and mainly used in aromatherapy. The chemical constituents and its antitumor activity on Triple-negative breast cancer (TNBC) was explored in the present study. Gas chromatography-mass spectrometry (GC/MS) was employed to analyze the chemical constituents of CEO. The cell viability, migration and invasion of TNBC cell MDA-MB-231 were measured using MTT, wound scratch and Transwell assay, respectively. The protein expression of PI3K/Akt/mTOR signaling pathway was determined by Western blot. CEO is rich in terpenoids (63.51 %), among which the identified terpenoids and their derivatives are mainly Caryophyllene (29.57 %), d-Cadinene (12.81 %), Caryophyllene oxide (14.51 %), etc. Three concentration of CEO (1, 1.5, 2 mu g/mL) significantly inhibited the proliferation, migration and invasion of MDA-MB-231 cells with a dose dependent manner. Moreover, the phosphorylation of PI3K, Akt and mTOR was inhibited by CEO. The results revealed that there was abundant terpenoids in the CEO which account for 63.51 %. CEO significantly inhibited the proliferation, migration and invasion of MDA-MB-231 cells, exhibiting antitumor effect on TNBC. The antitumor effect of CEO might attribute to its inhibition on PI3K/Akt/mTOR signaling pathway. However, further study should be conducted in more TNBC cell lines and animal models to provide further evidence for TNBC treatment by CEO.
引用
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页数:10
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