Apoptosis Induction of Agave lechuguilla Torrey Extract on Human Lung Adenocarcinoma Cells (SK-LU-1)

被引:17
作者
Alberto Anguiano-Sevilla, Luis [1 ,2 ]
Lugo-Cervantes, Eugenia [3 ]
Ordaz-Pichardo, Cynthia [4 ]
Luis Rosas-Trigueros, Jorge [5 ]
Eugenia Jaramillo-Flores, Maria [1 ,2 ]
机构
[1] IPN, Escuela Nacl Ciencias Biol, Mexico City 07738, DF, Mexico
[2] Alcaldia Gustavo A Madero, Unidad Profes Lopez Mateos, Av Wilfrido Massieu Esq Cda Manuel Stampa S-N Col, Mexico City 07738, DF, Mexico
[3] CIATEJ, Ctr Invest & Asistencia Tecnol & Diseno Estado Ja, Camino Arenero 1227, Zapopan 45019, Mexico
[4] Alcaldia Gustavo A Madero, IPN, Escuela Nacl Med & Homeopatia, Guillermo Massieu Helguera 239, Mexico City 07320, DF, Mexico
[5] Alcaldia Gustavo A Madero, Unidad Profes Lopez Mateos, IPN, Escuela Super Comp, Juan Dios Batiz & Miguel Othon Mendizabal S-N Col, Mexico City 07738, DF, Mexico
关键词
Agave lechuguilla; apoptosis; cytotoxic activity; molecular docking; mass spectrometry; MASS-SPECTROMETRY; AIR-POLLUTION; CANCER; QUANTIFICATION; FRAGMENTATION; CHEMISTRY; TOXICITY; PATHWAYS; BCL-2; ASSAY;
D O I
10.3390/ijms19123765
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
In this study, an ethanol extract of Agave lechuguilla was evaluated against six carcinogenic cell lines (HCT-15, MCF-7, PC-3, U-251, SK-LU-1 and K-562) with an inhibition of 75.7 +/- 2.3% against the SK-LU-1 line. Based on the previous result, the extract was hydrolyzed and fractionated, to which the IC50 was determined; the cell line was more sensitive to the fractionated extract with an IC50 6.96 +/- 0.15 mu g/mL. Characterization by mass spectrometry showed the presence of kaempferol, quercetin and a flavonoid dimer formed by afzelechin-4 beta-8-quercetin, according to the generated fragmentation pattern. The fractionated extract presented cell death by apoptosis with 39.8% at 24 h. Molecular docking was performed with the molecules found to try to describe cell death by apoptosis through death receptors such as FasCD95, TNF-R1, DR4/5 and blocking signaling on the EGFR and K-Ras MAPK/ERK pathway, as well as through the intrinsic pathway activating tBID, which promotes the amplification of the apoptotic signal due to the activation of caspase-3, and consequently caspase-7. In addition to the activation of the IIb complex associated with cell death due to necroptosis.
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页数:24
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