In Vitro Antiproliferative Activity of Echinulin Derivatives from Endolichenic Fungus Aspergillus sp. against Colorectal Cancer

被引:0
|
作者
Makhloufi, Hind [1 ]
Pinon, Aline [1 ]
Champavier, Yves [2 ]
Saliba, Jennifer [3 ]
Millot, Marion [1 ]
Fruitier-Arnaudin, Ingrid [3 ]
Liagre, Bertrand [1 ]
Chemin, Guillaume [1 ]
Mambu, Lengo [1 ]
机构
[1] Univ Limoges, Fac Pharm, LABCiS, UR 22722, F-87000 Limoges, France
[2] Univ Limoges, CHU Limoges, CNRS, Inserm,UAR 2015,BISCEm,US 42, F-87025 Limoges, France
[3] Univ Rochelle, CNRS, Lab LIENSs, UMR 7266, F-17000 La Rochelle, France
来源
MOLECULES | 2024年 / 29卷 / 17期
关键词
endolichenic fungi; Aspergillus sp; human colorectal cancer; chemoresistant cancers; DIKETOPIPERAZINE ALKALOIDS; METABOLITES; CHEVALIERI;
D O I
10.3390/molecules29174117
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
The endolichenic fungus Aspergillus sp. was isolated from the lichen Xanthoparmelia conspersa harvested in France. Aspergillus sp. was grown on a solid culture medium to ensure the large-scale production of the fungus with a sufficient mass of secondary metabolites. The molecular network analysis of extracts and subfractions enabled the annotation of 22 molecules, guiding the purification process. The EtOAc extract displayed an antiproliferative activity of 3.2 +/- 0.4 mu g/mL at 48 h against human colorectal cancer cells (HT-29) and no toxicity at 30 mu g/mL against human triple-negative breast cancer (TNBC) cells (MDA-MB-231) and human embryonic kidney (HEK293) non-cancerous cells. Among the five prenylated compounds isolated, of which four are echinulin derivatives, compounds 1 and 2 showed the most important activity, with IC50 values of 1.73 mu M and 8.8 mu M, respectively, against HT-29 cells.
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页数:17
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