Estrogen receptor alpha (ER-α) antagonistic activity of phytoconstituents from Potentilla atrosanguinea and Potentilla fulgens in breast cancer

被引:0
作者
Kumar, Amit [1 ]
Verma, Harkomal [2 ]
Gangwar, Prabhakar [2 ]
Jangid, Kailash [3 ]
Kumar, Vinod [3 ]
Dhiman, Monisha [4 ]
Jaitak, Vikas [1 ]
机构
[1] Cent Univ Punjab, Dept Pharmaceut Sci & Nat Prod, Nat Prod Chem Lab, Bathinda 151401, India
[2] Cent Univ Punjab, Dept Zool, Bathinda 151401, India
[3] Cent Univ Punjab, Dept Chem, Bathinda 151401, India
[4] Cent Univ Punjab, Dept Microbiol, Bathinda 151401, India
关键词
Breast cancer; Potentilla; Estrogen receptor; Antiestrogenic activity; In silico; HPTLC; PROPHYLACTIC AGENT; BIOLOGICAL EVALUATION; BETA-SITOSTEROL; PROTEIN; ANTIOXIDANT; ANTICANCER; ORBITALS; DOCKING; HYBRIDS; DESIGN;
D O I
10.1016/j.fitote.2024.106123
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The Potentilla genus has long been used traditionally as food and a folklore medicine. In the present study, aerial parts of two Potentilla species, Potentilla fulgens and Potentilla atrosanguinea, of western Himalayan origin, were studied for their anti-breast cancer activity. Ethyl acetate (PAA-EA, PFA-EA), methanolic (PAA-ME, PFA-ME) and hydro-methanolic extract (PAA-HM, PFA-HM) of the plants were tested for their antiproliferative activities against MCF-7 and T-47D breast cancer cell lines. The extracts showed good antiproliferative activity against ER alpha dominant breast cancer cell line T-47D, having IC50 values 6.19 +/- 0.01 to 33.23 +/- 0.04 mu g/ml. Eight compounds were isolated, characterized, and quantified from ethyl acetate and methanolic extracts by column chromatography, 1D, 2D-NMR, HRMS and TLC densitometric analysis. Two compounds (4 and 6) have shown better antiproliferative activity than standard bazedoxifene and were further evaluated for their ER-alpha binding affinity via-fluorescence polarization-based competitive binding assay. The antiestrogenic properties of both compounds were assessed using western blotting. Compounds 4 and 6 were found to have significant affinity for the ER-alpha and managed to decrease its expression by 38 and 54% respectively. Compounds 4 and 6 also had good stability and reactivity as measured by minimal fluctuations in molecular dynamic simulation analysis, a good dock score in molecular docking, and a respectable HOMO-LUMO energy gap in DFT calculations. Compounds 4 and 6 have shown reliable results and can be used in the development of natural product-based anti-breast cancer agents.
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页数:13
相关论文
共 77 条
[1]   Analysis of estrogen receptor isoforms and variants in breast cancer cell lines [J].
Al-Bader, Maie ;
Ford, Christopher ;
Al-Ayadhy, Bushra ;
Francis, Issam .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2011, 2 (03) :537-544
[2]  
Anal J. M. H., 2014, Journal of Chemical and Pharmaceutical Research, V6, P89
[3]   Phytochemical Profiling of Extracts from Rare Potentilla Species and Evaluation of Their Anticancer Potential [J].
Augustynowicz, Daniel ;
Lemieszek, Marta Kinga ;
Strawa, Jakub Wladyslaw ;
Wiater, Adrian ;
Tomczyk, Michal .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (05)
[4]   Synthesis, quantum chemical study, AIM simulation, in silico ADMET profile analysis, molecular docking and antioxidant activity assessment of aminofuran derivatives [J].
Azad, Iqbal ;
Akhter, Yusuf ;
Khan, Tahmeena ;
Azad, Mohammad Irfan ;
Chandra, Subhash ;
Singh, Praveer ;
Kumar, Durgesh ;
Nasibullah, Malik .
JOURNAL OF MOLECULAR STRUCTURE, 2020, 1203
[5]   Role of dietary bioactive natural products in estrogen receptor-positive breast cancer [J].
Bak, Min Ji ;
Das Gupta, Soumyasri ;
Wahler, Joseph ;
Suh, Nanjoo .
SEMINARS IN CANCER BIOLOGY, 2016, 40-41 :170-191
[6]   Antimicrobial flavonoids as a potential substitute for overcoming antimicrobial resistance [J].
Biharee, Avadh ;
Sharma, Aditi ;
Kumar, Amit ;
Jaitak, Vikas .
FITOTERAPIA, 2020, 146
[7]  
Blumenthal M., 1998, COMPLETE GERMAN COMM
[8]   Jaguar: A high-performance quantum chemistry software program with strengths in life and materials sciences [J].
Bochevarov, Art D. ;
Harder, Edward ;
Hughes, Thomas F. ;
Greenwood, Jeremy R. ;
Braden, Dale A. ;
Philipp, Dean M. ;
Rinaldo, David ;
Halls, Mathew D. ;
Zhang, Jing ;
Friesner, Richard A. .
INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2013, 113 (18) :2110-2142
[9]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21609, 10.3322/caac.21492]
[10]   Best-Practice DFT Protocols for Basic Molecular Computational Chemistry [J].
Bursch, Markus ;
Mewes, Jan-Michael ;
Hansen, Andreas ;
Grimme, Stefan .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2022, 61 (42)