INDUCTION OF CELL CYCLE ARREST AND APOPTOSIS BY ORMENIS ERIOLEPIS A MORROCAN ENDEMIC PLANT IN VARIOUS HUMAN CANCER CELL LINES.

Lamiae Belayachi, Clara Aceves-Luquero, Nawel Merghoub, Silvia Fernández de Mattos, Saaîd Amzazi, Priam Villalonga, Youssef Bakri
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引用次数: 15

Abstract

Background: Ormenis eriolepis Coss (Asteraceae) is an endemic Moroccan subspecies, traditionally named "Hellala" or "Fergoga". It's usually used for its hypoglycemic effect as well as for the treatment of stomacal pain. As far as we know, there is no scientific exploration of anti tumoral activity of Ormenis eriolepis extracts.

Materials and methods: In this regard, we performed a screening of organic extracts and fractions in a panel of both hematological and solid cancer cell lines, to evaluate the potential in vitro anti tumoral activity and to elucidate the respective mechanisms that may be responsible for growth arrest and cell death induction. The plant was extracted using organic solvents, and four different extracts were screened on Jurkat, Jeko-1, TK-6, LN229, SW620, U2OS, PC-3 and NIH3T3 cells.

Results: Cell viability assays revealed that, the IC50 values were (11,63±5,37μg/ml) for Jurkat, (13,33±1,67μg/ml) for Jeko-1, (41,67±1,98μg/ml) for LN229 and (19,31±4,88μg/ml) for PC-3 cells upon treatment with Oe-DF and Oe-HE respectively. Both the fraction and extract exhibited no effects on TK6 and NIH3T3. Cytometry analysis accompanied by DNA damage signaling protein levels monitoring (p-H2A.X), showed that both the Dichloromethane Fraction and Hexanic extract induce DNA double stranded breaks (DSBs) accompanied by cell cycle arrest in G1 (Jurkat, Jeko -1 and LN22) and G2/M (PC-3) phases which is agreed with the caspase activity observed. Additional experiments with selective inhibitors of stress and survival pathways (JNK, MAPK, Rho, p53, and JAK3) indicated that none of these pathways was significantly involved in apoptosis induction. The bioactive compound analysis by CG/MS indicated that the major compounds in Oe-DF were: Linoleic Acid (15,89%), Podophyllotoxin (17,89%) and Quercetin (22,95%). For Oe-HE the major molecules were: Linoleic Acid (9,76%), α-curcumene (7,07%), α-bisabolol (5,49%), Campesterol (4,41%), Stigmasterol (14,08%) and β-sitosterol (7,49%).

Conclusion: Our data suggest that bioactive compounds present in Ormenis eriolepis show significant anti proliferative activity inducing cell cycle arrest and cell death operating through apoptosis pathway.

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摩洛哥特有植物鸢尾对人肿瘤细胞系细胞周期阻滞和凋亡的诱导作用。
背景:Ormenis eriolepis Coss (Asteraceae)是摩洛哥特有的亚种,传统上被称为“Hellala”或“Fergoga”。它通常用于降糖和治疗胃痛。据我们所知,还没有科学的探索鸢尾提取物的抗肿瘤活性。材料和方法:在这方面,我们在一组血液学和实体癌细胞系中进行了有机提取物和馏分的筛选,以评估其潜在的体外抗肿瘤活性,并阐明可能导致生长停滞和细胞死亡的各自机制。采用有机溶剂提取,在Jurkat、Jeko-1、TK-6、LN229、SW620、U2OS、PC-3和NIH3T3细胞上筛选4种不同的提取物。结果:细胞活力测定显示,经Oe-DF和Oe-HE处理后,Jurkat细胞的IC50值分别为(11,63±5,37μg/ml)、Jeko-1细胞的IC50值为(13,33±1,67μg/ml)、LN229细胞的IC50值为(41,67±1,98μg/ml)和PC-3细胞的IC50值分别为(19,31±4,88μg/ml)。提取物和提取物对TK6和NIH3T3均无明显影响。细胞分析和DNA损伤信号蛋白水平监测(p-H2A.X)显示,二氯甲烷组分和己烷提取物均诱导DNA双链断裂(DSBs),并伴有G1期(Jurkat, Jeko -1和LN22)和G2/M期(PC-3)细胞周期阻滞,这与观察到的caspase活性一致。对应激和生存途径(JNK、MAPK、Rho、p53和JAK3)的选择性抑制剂进行的进一步实验表明,这些途径均未显著参与细胞凋亡诱导。经质谱分析,其主要活性成分为亚油酸(15.89%)、鬼臼毒素(17.89%)和槲皮素(22.95%)。e- he的主要分子为:亚油酸(9.76%)、α-姜黄烯(7.07%)、α-双abolol(5.49%)、油菜甾醇(4.41%)、豆甾醇(14.08%)和β-谷甾醇(7.49%)。结论:鸢尾草中含有的生物活性物质具有明显的抗增殖活性,通过凋亡途径诱导细胞周期阻滞和细胞死亡。
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