Isolation of Chlorogenic Acid from Soil Borne Fungi Screlotium rolfsii, their Reversal of Multidrug Resistance and Anti-proliferative in Mouse Lymphoma Cells

被引:10
作者
Ahmad, Bashir [1 ]
Rizwan, Muhammad [1 ]
Rauf, Abdur [2 ]
Raza, Muslim [3 ]
Bashir, Shumaila [4 ]
Molnar, Joseph [5 ]
Csonka, Akos [5 ]
Szabo, Diana [6 ]
Mubarak, Mohammad S. [7 ]
Noor, Mah [1 ]
Siddiqui, Bina S. [8 ]
机构
[1] Univ Peshawar, Ctr Biotechnol & Microbiol, Peshawar 25120, Kpk, Pakistan
[2] Univ Swabi, Dept Chem, Anbar 23561, Khyber Pakhtunk, Pakistan
[3] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, 15 East Rd North Third Ring, Beijing 100029, Peoples R China
[4] Univ Peshawar, Dept Pharm, Peshawar 25120, Pakistan
[5] Univ Szeged, Fac Med, Dept Med Microbiol & Immunobiol, Dom Ter 10, H-6720 Szeged, Hungary
[6] Univ Szeged, Fac Med, Dept Otorhinolaryngol Head & Neck Surg, Tisza L Krt 111, H-6725 Szeged, Hungary
[7] Univ Jordan, Dept Chem, Amman 11942, Jordan
[8] Univ Karachi, Int Ctr Chem & Biol Sci, HEJ Res Inst Chem, Karachi 75270, Pakistan
关键词
Chlorogenic acid; fungi; glycoprotein; Multidrug Resistance (MDR); Screlotium rolfsii; secondary metabolites; P-GLYCOPROTEIN; ABC TRANSPORTERS; DOCKING; CANCER; MEMBRANE; BINDING; PROTEIN; SITES;
D O I
10.2174/1573406413666170612110443
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Fungi performing a wide range of function in soil by secreting low molecular weight compound known as secondary metabolites. S. rolfsii is a soil borne phytopathogenic fungi was used for the production of bioactive compounds. Objective: The present study belongs to evaluate the anticancer potentials of a secondary metabolites isolated from S. rolfsii, their multidrug resistance (MDR), and molecular docking study. Method: (1S,3R,4R,5R,E)-3-(3-(3,4-Dihydroxyphenyl) acryloyloxy)-1,4,5 trihydroxycyclohexane-carboxylic acid (1), or best known as chlorogenic acid, was isolated from the ethyl acetate fraction of crude secondary metabolites produced by the soil borne Fungus Screlotium rolfsii. Structure of chlorogenic acid (1) was confirmed by means of FT-IR, H-1 NMR, C-13 NMR, and mass spectrometry as well as by melting point. Results: Effect of compound 1 on the reversion of multidrug resistant (MDR) mediated by P-glycoprotein (P-gp) against cancer cells was evaluated with a rhodamine-123 exclusion screening test on human mdr1 gene transfected mouse gene transfected L5178 and L5178Y mouse T-cell lymphoma. Compound 1 was also evaluated for Anti-proliferative effect on the L5178 mouse T-cell lymphoma cell line. Conclusion: Results from the present investigation revealed that compound 1 exhibits excellent MDR reversing effect in a dose-dependent manner against mouse T-lymphoma cell line. Compound 1 also showed anti-proliferative effect on L5178Y mouse T-lymphoma cell line.
引用
收藏
页码:721 / 726
页数:6
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