Antiproliferative potential of moluccella laevis L. aerial parts family lamiaceae (labiatae), supported by phytochemical investigation and molecular docking study

被引:11
作者
Hamed, Ashraf N. E. [1 ]
Abdelaty, Nousiba A. [1 ]
Attia, Eman Z. [1 ]
Amin, Mohamed N. [2 ]
Ali, Taha F. S. [3 ]
Afifi, Ahmed H. [4 ]
Abdelmohsen, Usama R. [1 ,5 ]
Desoukey, Samar Y. [1 ]
机构
[1] Minia Univ, Fac Pharm, Dept Pharmacognosy, Al Minya, Egypt
[2] Mansoura Univ, Fac Pharm, Dept Biochem, Mansoura, Egypt
[3] Minia Univ, Fac Pharm, Dept Med Chem, Al Minya, Egypt
[4] Natl Res Ctr, Dept Pharmacognosy, Div Pharmaceut Ind, Giza, Dokki, Egypt
[5] Deraya Univ, Fac Pharm, Dept Pharmacognosy, New Minia, Egypt
关键词
Moluccella laevis; Lamiaceae (Labiatae); cytotoxic; metabolomic; phytochemical; molecular docking;
D O I
10.1080/14786419.2021.1876046
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The current biologically guided study aimed the in vitro investigation of cytotoxic activity, identification of the phytochemical content of Moluccella laevis L. aerial parts and supporting this activity by a molecular docking study. Aqueous fraction demonstrated the most potent cytotoxic effect against CACO-2 with IC50 = 0.067 +/- 0.01 mu g/mL. Furthermore, EtOAc fraction showed a remarkable cytotoxic activity against MCF-7 cell line with IC50 = 0.35 +/- 0.02 mu g/mL. Consequently, total ethanolic extract (TEE) and its fractions were subjected to LC-HR-ESI-MS metabolic profiling to discover the constituents that possibly underlie their cytotoxicity. Twenty compounds were tentatively identified from metabolic analysis. Furthermore, eight compounds were isolated. In silico docking study revealed that stachydrine is more likely to account for the antiproliferative activity of both EtOAc and aqueous fractions, probably via its moderate inhibition of receptor tyrosine kinases.
引用
收藏
页码:1391 / 1395
页数:5
相关论文
共 16 条
[1]   Anti-angiogenic activity of Middle East medicinal plants of the Lamiaceae family [J].
Abdallah, Qasem ;
Al-Deeb, Ibrahim ;
Bader, Ammar ;
Hamam, Fayez ;
Saleh, Kamel ;
Abdulmajid, Amin .
MOLECULAR MEDICINE REPORTS, 2018, 18 (02) :2441-2448
[2]   Discovery of novel thienoquinoline-2-carboxamide chalcone derivatives as antiproliferative EGFR tyrosine kinase inhibitors [J].
Abdelbaset, Mahmoud S. ;
Abdel-Aziz, Mohamed ;
Ramadan, Mohamed ;
Abdelrahman, Mostafa H. ;
Bukhari, Syed Nasir Abbas ;
Ali, Taha F. S. ;
Abuo-Rahma, Gamal El-Din A. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2019, 27 (06) :1076-1086
[3]   A review of pharmacological and pharmacokinetic properties of stachydrine [J].
Cheng, Fang ;
Zhou, Yanxi ;
Wang, Miao ;
Guo, Chuanjie ;
Cao, Zhixing ;
Zhang, Ruoqi ;
Peng, Cheng .
PHARMACOLOGICAL RESEARCH, 2020, 155
[4]  
El-Sayyad S., 1999, Bull. Pharm. Sci. AUN, V22, P123
[5]   Chemical characterization and anti-inflammatory activity of luteolin glycosides isolated from lemongrass [J].
Francisco, Vera ;
Figueirinha, Artur ;
Costa, Gustavo ;
Liberal, Joana ;
Lopes, Maria Celeste ;
Garcia-Rodriguez, Carmen ;
Geraldes, Carlos F. G. C. ;
Cruz, Maria T. ;
Batista, Maria T. .
JOURNAL OF FUNCTIONAL FOODS, 2014, 10 :436-443
[6]   Roles of ERBB family receptor tyrosine kinases, and downstream signaling pathways, in the control of cell growth and survival [J].
Grant, S ;
Qiao, L ;
Dent, P .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2002, 7 :D376-D389
[7]  
Hassan M., 2016, Leaves. Journal of Medicinal Plants Research, V10, P232
[8]  
Hedge I.C., 1992, ADV LABIATAE SCI, P7
[9]   Cytotoxicity of flavonoids toward cultured normal human cells [J].
Matsuo, M ;
Sasaki, N ;
Saga, K ;
Kaneko, T .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2005, 28 (02) :253-259
[10]   A new cytotoxic iridoid from Callicarpa nudiflora [J].
Mei, Wen-Li ;
Han, Zhuang ;
Cui, Hai-Bin ;
Zhao, You-Xing ;
Deng, Yuan-Yuan ;
Dai, Hao-Fu .
NATURAL PRODUCT RESEARCH, 2010, 24 (10) :899-904