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28-O-丙炔酰桦木醇对人黑色素性和无黑色素性黑色素瘤细胞增殖及凋亡的影响

Influence of 28-O-propynoylbetulin on proliferation and apoptosis of melanotic and amelanotic human melanoma cells.

作者信息

Kaps Anna, Chodurek Ewa, Orchel Arkadiusz, Jaworska-Kik Marzena, Bębenek Ewa, Boryczka Stanisław, Kasperczyk Janusz

机构信息

Department of Biopharmacy, Medical University of Silesia in Katowice, School of Pharmacy with the Division of Laboratory Medicine, Sosnowiec, Poland.

Department of Organic Chemistry, Medical University of Silesia in Katowice, School of Pharmacy with the Division of Laboratory Medicine, Sosnowiec, Poland.

出版信息

Postepy Hig Med Dosw (Online). 2016 Dec 31;70(0):1404-1408. doi: 10.5604/17322693.1227678.

Abstract

INTRODUCTION

A relatively new approach in treatment of malignant melanoma is the use of betulin and its synthetic derivatives that have anticancer properties. The aim of the study was to determine the effect of an acetylenic derivative of betulin, 28-O-propynoylbetulin, on cell growth and apoptosis induction in human melanotic and amelanotic melanoma cells.

MATERIALS AND METHODS

The A2058 and C32 cell lines were incubated with 28-O-propynoylbetulin (working solutions from 0.1 to 10 μg/ml). To evaluate cell proliferation, a sulforhodamine B based assay was conducted. In order to elucidate the early stages of apoptosis in both melanoma cell lines, caspase-3 activity was evaluated.

RESULTS

The administration of 28-O-propynoylbetulin at a concentration equal to or less than 1 μg/ml did not cause a statistically significant change in the cell proliferation in either melanoma cell line (compared to control, p>0.05). Higher concentrations of the compound (3 and 10 μg/ml) inhibited the cell growth (in comparison to control, p<0.05). These results corresponded with caspase-3 activity results that revealed an increase of enzyme activity after 24-hour incubation with 3 and 10 μg/ml of the compound (compared to control, p<0.05).

DISCUSSION

The study revealed that 28-O-propynoylbetulin may have diverse effects on melanoma cells and could be a strong inhibitor of cell growth (C32 cells) or exert a more potent proapoptotic effect (A2058 cells). These findings support the possibility of the use of EB5 in different antimelanoma approaches.

摘要

引言

治疗恶性黑色素瘤的一种相对较新的方法是使用具有抗癌特性的桦木醇及其合成衍生物。本研究的目的是确定桦木醇的炔属衍生物28 - O - 丙炔酰桦木醇对人黑素性和无黑素性黑色素瘤细胞生长及凋亡诱导的影响。

材料与方法

将A2058和C32细胞系与28 - O - 丙炔酰桦木醇(工作溶液浓度为0.1至10μg/ml)一起孵育。为评估细胞增殖,进行了基于磺酰罗丹明B的检测。为阐明两种黑色素瘤细胞系凋亡的早期阶段,评估了半胱天冬酶 - 3的活性。

结果

给予浓度等于或低于1μg/ml的28 - O - 丙炔酰桦木醇,两种黑色素瘤细胞系的细胞增殖均未发生统计学上的显著变化(与对照组相比,p>0.05)。该化合物的较高浓度(3和10μg/ml)抑制了细胞生长(与对照组相比,p<0.05)。这些结果与半胱天冬酶 - 3活性结果相符,该结果显示在与3和10μg/ml的该化合物孵育24小时后酶活性增加(与对照组相比,p<0.05)。

讨论

该研究表明28 - O - 丙炔酰桦木醇可能对黑色素瘤细胞有多种作用,可能是细胞生长的强抑制剂(C32细胞)或发挥更强的促凋亡作用(A2058细胞)。这些发现支持了在不同抗黑色素瘤方法中使用EB5的可能性。

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