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氧化型低密度脂蛋白联合阿霉素对食管癌细胞株 Eca-109 增殖的影响。

The effect of oxidized low-density lipoprotein combined with adriamycin on the proliferation of Eca-109 cell line.

机构信息

Qilu Hospital, Shandong University, Jinan, P.R. China.

出版信息

Lipids Health Dis. 2011 Jun 29;10:108. doi: 10.1186/1476-511X-10-108.

DOI:10.1186/1476-511X-10-108
PMID:21711568
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3150309/
Abstract

BACKGROUND

The purpose of this study was to identify the affect on the proliferation Eca-109 cells treated with oxidized low-density lipoprotein (ox-LDL) combined with adriamycin (ADM).

METHODS

Eca-109 cell were cultured in the presence of oxLDL/ADM, and cell proliferation tested by MTT and cell apoptosis was monitored by the proportion of apoptosis and cell cycle by flow cytomester. We simultaneously evaluated the level of associated- apoptosis Bcl-2, Bax, and Caspase-3 gene mRNA and protein.

RESULTS

OxLDL were cytotoxic and activate apoptosis. OxLDL combined with ADM significant enhanced the proportion rate of apoptosis on a time and dose dependency. The expressions of the inhibiting apoptosis Bcl-2 gene mRNA and protein were down regulated, whereas, the expressions of the promoting apoptosis Bax, and Caspase-3 genes mRNA and protein were up regulation.

CONCLUSION

These results suggested that oxLDL have cytotoxicity and activate apoptosis on the Eca-109 cells. OxLDL combined with ADM have a synergistic effect on the apoptosis induced Eca-109 cells. Furthermore, oxLDL may contribute to the improvement of clinical chemotherapy of cancer need to make further investigation.

摘要

背景

本研究旨在探讨氧化型低密度脂蛋白(ox-LDL)与阿霉素(ADM)联合作用对食管癌细胞(Eca-109)增殖的影响。

方法

将 Eca-109 细胞分别在 oxLDL/ADM 存在的条件下进行培养,通过 MTT 法检测细胞增殖情况,采用流式细胞术检测细胞凋亡比例和细胞周期,同时检测相关凋亡基因 Bcl-2、Bax 和 Caspase-3 的 mRNA 和蛋白表达水平。

结果

ox-LDL 具有细胞毒性,并能诱导细胞凋亡。ox-LDL 联合 ADM 呈时间和剂量依赖性显著增强细胞凋亡的比例。抑制凋亡基因 Bcl-2 的 mRNA 和蛋白表达下调,而促进凋亡基因 Bax 和 Caspase-3 的 mRNA 和蛋白表达上调。

结论

这些结果表明 ox-LDL 对 Eca-109 细胞具有细胞毒性和促凋亡作用,ox-LDL 联合 ADM 对诱导 Eca-109 细胞凋亡具有协同作用。ox-LDL 可能有助于改善癌症的临床化疗效果,需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/391ec0052757/1476-511X-10-108-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/b602e13faa52/1476-511X-10-108-1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/a4b1775b84d1/1476-511X-10-108-3.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/5c8417ff4599/1476-511X-10-108-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/6d274ee032b2/1476-511X-10-108-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/391ec0052757/1476-511X-10-108-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/b602e13faa52/1476-511X-10-108-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/1121fa44e90f/1476-511X-10-108-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/a4b1775b84d1/1476-511X-10-108-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/be5653b8ab43/1476-511X-10-108-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/5c8417ff4599/1476-511X-10-108-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/6d274ee032b2/1476-511X-10-108-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c3/3150309/391ec0052757/1476-511X-10-108-7.jpg

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