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
收藏
页数:10
相关论文
共 50 条
  • [1] Jolkinolide B induces apoptosis in MDA-MB-231 cells through inhibition of the PI3K/Akt signaling pathway
    Lin, Yu
    Cui, Hongxia
    Xu, Huiyu
    Yue, Liling
    Xu, Hao
    Jiang, Liyan
    Liu, Jicheng
    ONCOLOGY REPORTS, 2012, 27 (06) : 1976 - 1980
  • [2] The combination of Curcumin and Doxorubicin on targeting PI3K/AKT/mTOR signaling pathway: an in vitro and molecular docking study for inhibiting the survival of MDA-MB-231
    Esha Sarkar
    Akanksha Kotiya
    Afreen Khan
    Rajabrata Bhuyan
    Syed Tasleem Raza
    Aparna Misra
    Abbas Ali Mahdi
    In Silico Pharmacology, 12 (2)
  • [3] DMC triggers MDA-MB-231 cells apoptosis via inhibiting protective autophagy and PI3K/AKT/mTOR pathway by enhancing ROS level
    Jiang, Yu
    Xu, Sunjie
    Guo, Miaomiao
    Lu, Zhi
    Wei, Xing
    An, Faliang
    Xin, Xiujuan
    TOXICOLOGY IN VITRO, 2024, 97
  • [4] Echinoside A from Pearsonothuria graeffei Exert the Cytotoxicity to MDA-MB-231 Cells via Mitochondrial Membrane and Modulation of PI3K/Akt/mTOR Pathway
    Li, Hongyan
    Cui, Huanhuan
    Cong, Peixu
    Xu, Jie
    Xie, Wancui
    Wang, Yuming
    Xue, Changhu
    JOURNAL OF OCEAN UNIVERSITY OF CHINA, 2023, 22 (01) : 205 - 212
  • [5] Echinoside A from Pearsonothuria graeffei Exert the Cytotoxicity to MDA-MB-231 Cells via Mitochondrial Membrane and Modulation of PI3K/Akt/mTOR Pathway
    LI Hongyan
    CUI Huanhuan
    CONG Peixu
    XU Jie
    XIE Wancui
    WANG Yuming
    XUE Changhu
    JournalofOceanUniversityofChina, 2023, 22 (01) : 205 - 212
  • [6] Echinoside A from Pearsonothuria graeffei Exert the Cytotoxicity to MDA-MB-231 Cells via Mitochondrial Membrane and Modulation of PI3K/Akt/mTOR Pathway
    Hongyan Li
    Huanhuan Cui
    Peixu Cong
    Jie Xu
    Wancui Xie
    Yuming Wang
    Changhu Xue
    Journal of Ocean University of China, 2023, 22 : 205 - 212
  • [7] Arachidonic acid promotes migration and invasion through a PI3K/Akt-dependent pathway in MDA-MB-231 breast cancer cells
    Villegas-Comonfort, Socrates
    Castillo-Sanchez, Rocio
    Serna-Marquez, Nathalia
    Cortes-Reynosa, Pedro
    Perez Salazar, Eduardo
    PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2014, 90 (05): : 169 - 177
  • [8] Total saponins of Bolbostemma paniculatum (maxim.) Franquet exert antitumor activity against MDA-MB-231 human breast cancer cells via inhibiting PI3K/Akt/mTOR pathway
    Dou, Jian-Wei
    Shang, Rong-Guo
    Lei, Xiao-Qin
    Li, Kang-Le
    Guo, Zhan-Zi
    Ye, Kai
    Yang, Xiao-Juan
    Li, Yu-Wei
    Zhou, Yun-Yun
    Yao, Jia
    Huang, Qian
    BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2019, 19 (01):
  • [9] Total saponins of Bolbostemma paniculatum (maxim.) Franquet exert antitumor activity against MDA-MB-231 human breast cancer cells via inhibiting PI3K/Akt/mTOR pathway
    Jian-Wei Dou
    Rong-Guo Shang
    Xiao-Qin Lei
    Kang-Le Li
    Zhan-Zi Guo
    Kai Ye
    Xiao-Juan Yang
    Yu-Wei Li
    Yun-Yun Zhou
    Jia Yao
    Qian Huang
    BMC Complementary and Alternative Medicine, 19
  • [10] Wikstromol fromWikstroemia indicainduces apoptosis and suppresses migration of MDA-MB-231 cells via inhibiting PI3K/Akt pathway
    Yao, Huankai
    Zhang, Xiuli
    Zhang, Nan
    Li, Jindong
    Li, Yan
    Wei, Qunli
    JOURNAL OF NATURAL MEDICINES, 2021, 75 (01) : 178 - 185