海洋软体动物褐斑鼓噪(Tympanatonus fuscatus Var radula)和耳厚黑藻(Pachymelania aurita)提取物体外抗增殖研究。

International journal of biochemistry and molecular biology Pub Date : 2019-04-15 eCollection Date: 2019-01-01
Queensley Eghianruwa, Omolaja Osoniyi, Sabina Wachira, Naomi Maina, Regina Mbugua, Mabel Imbuga
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引用次数: 0

摘要

本研究旨在研究尼日利亚尼日尔三角洲地区常见的两种海洋软体动物的粗丙酮-甲醇和水提取物的抗有丝分裂和抗增殖活性;fuscatus和P.aurita对人癌细胞(DU145, Hep-2和HCC1395)细胞系的体外杀伤作用。利用葱根分生组织细胞对提取物的抗有丝分裂活性进行了评价。用VeroE6法比较了植物提取物对肿瘤细胞株的抗增殖活性。以阿霉素为阳性对照。采用qPCR技术对促凋亡基因CASP3、CASP8和P53进行基因表达研究。黄霉醇提物(TFAC)对DU145、HCC 1395、Hep2的IC50分别为96.48±1.36 μg/ml、61.44±2.45 μg/ml和0.52±0.36 μg/ml,对DU145、HCC 1395和Hep-2的选择性指数分别为4.94、7.78和921.97,均有较好的抑制作用。此外,TFAC是唯一显著上调caspase 3、caspase 8和P53表达的提取物。因此,这些发现提示TFAC作为抗癌剂的潜在开发潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In vitro antiproliferative studies of extracts of the marine molluscs: Tympanatonus fuscatus Var radula (linnaeus) and Pachymelania aurita (muller).

In vitro antiproliferative studies of extracts of the marine molluscs: Tympanatonus fuscatus Var radula (linnaeus) and Pachymelania aurita (muller).

In vitro antiproliferative studies of extracts of the marine molluscs: Tympanatonus fuscatus Var radula (linnaeus) and Pachymelania aurita (muller).

This study aimed to investigate the antimitotic and antiproliferation activities of crude acetone-methanol and aqueous extracts of two marine molluscs commonly found in the Niger Delta region of Nigeria; T.fuscatus and P.aurita, against human cancerous cell lines (DU145, Hep-2, and HCC1395) cell lines in vitro. The antimitotic activity of the extracts was evaluated using Allium cepa root meristematic cells. Antiproliferative activity of the plant extracts against the cancerous cell lines was compared with normal cell line (VeroE6). Doxorubicin was used as a positive control. Gene expression studies using qPCR for the proapoptotic genes, CASP3, CASP8 and P53 were also carried out. The alcohol extract of T.fuscatus (TFAC) exhibited the most promising activity against all the cancer cell lines tested (DU145 IC50 = 96.48 ± 1.36 μg/ml, HCC 1395 IC50 = 61.44 ± 2.45 μg/ml, Hep2 IC50 = 0.52 ± 0.36 μg/ml) and also had the highest selectivity index of 4.94, 7.78 and 921.97 for DU145, HCC 1395 and Hep-2 cells respectively. Furthermore, TFAC was the only extract that significantly upregulated the expression of caspase 3, caspase 8 and P53. Thus, these findings suggest potential exploitation of TFAC as an anticancer agent.

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