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蟹壳提取物诱导前列腺癌细胞系(LNcap)凋亡并减少一氧化氮分泌。

Crab Shell Extract Induces Prostate Cancer Cell Line (LNcap) Apoptosis and Decreases Nitric Oxide Secretion.

作者信息

Rezakhani Leila, Khazaei Mohammad Rasool, Ghanbari Ali, Khazaei Mozafar

机构信息

Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Fertility and Infertility Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

Cell J. 2017 Jul-Sep;19(2):231-237. doi: 10.22074/cellj.2016.4879. Epub 2017 Feb 22.

Abstract

OBJECTIVE

Prostate cancer is the second most common cancer worldwide. Chemotherapeutic agents have been shown to have adverse side-effects, and natural compounds have been recommended for cancer treatment, nowadays. Crab shell has been shown to have cancer preventative and suppressive effects and . The aim of present study was to investigate the effect of crab shell extract on prostate cancer cell line (LNcap) .

MATERIALS AND METHODS

In this experimental study, LNcap cells were treated with different concentrations (0, 100, 200, 400, 800 and 1000 µg/ml) of crab shell hydroalcoholic extract in three different culture periods (24, 48 and 72 hours). LNcap viability was evaluated by trypan blue staining and MTT assay. Cell apoptosis and nitric oxide (NO) secretion were determined by TUNEL and Griess assays, respectively. Data were analyzed by one-way ANOVA test and P<0.05 was considered significant.

RESULTS

LNcap viability was decreased dose- and time-dependently. Thus 400, 800, and 1000 µg/ml doses showed significant differences compared to control group (P<0.001). Dose-dependent increase in the apoptotic index was also observed in 800 and 1000 µg/ ml concentrations (P<0.001). Nitric oxide secretion of LNcap cell was decreased time- and dose-dependently, while it was significant for 1000 µg/ml (P<0.05).

CONCLUSION

Crab shell extract showed anti-prostate cancer effect, by inducing cell apop- tosis and decreasing NO production.

摘要

目的

前列腺癌是全球第二大常见癌症。化疗药物已被证明有不良副作用,如今天然化合物已被推荐用于癌症治疗。蟹壳已被证明具有癌症预防和抑制作用。本研究的目的是调查蟹壳提取物对前列腺癌细胞系(LNcap)的影响。

材料与方法

在本实验研究中,LNcap细胞在三个不同培养时间段(24、48和72小时)用不同浓度(0、100、200、400、800和1000µg/ml)的蟹壳水醇提取物处理。通过台盼蓝染色和MTT法评估LNcap活力。分别通过TUNEL法和Griess法测定细胞凋亡和一氧化氮(NO)分泌。数据通过单因素方差分析进行分析,P<0.05被认为具有显著性。

结果

LNcap活力呈剂量和时间依赖性降低。因此,400、800和1000µg/ml剂量与对照组相比有显著差异(P<0.001)。在800和1000µg/ml浓度下也观察到凋亡指数呈剂量依赖性增加(P<0.001)。LNcap细胞的一氧化氮分泌呈时间和剂量依赖性降低,而1000µg/ml时具有显著性(P<0.05)。

结论

蟹壳提取物通过诱导细胞凋亡和减少NO产生显示出抗前列腺癌作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de01/5412781/47e55ca971f4/Cell-J-19-231-g01.jpg

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