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熊果酸通过调控 Huh-7 细胞的 PI3K/Akt 和 MAPK 信号通路诱导细胞凋亡。

Ursolic Acid-Induced Apoptosis via Regulation of the PI3K/Akt and MAPK Signaling Pathways in Huh-7 Cells.

机构信息

Department of Anesthesiology, Changhua Christian Hospital, Changhua 50006, Taiwan.

Transplant Medicine & Surgery Research Center, Changhua Christian Hospital, Changhua 50006, Taiwan.

出版信息

Molecules. 2018 Aug 13;23(8):2016. doi: 10.3390/molecules23082016.

DOI:10.3390/molecules23082016
PMID:30104508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6222435/
Abstract

Ursolic acid (UA), is a kind of triterpene acid that exhibits wide biological properties. In this article, the effects of UA on apoptosis and the proliferation of human hepatoma Huh-7 cells were reported. The MTT results showed that cell viability of Huh-7 was reduced in a concentration and time-dependent effect. In addition, DAPI staining was used to detected condensation of chromatin in nucleus. Apoptotic cell population was examined using Annexin V/PI staining. The results showed that exposure to UA affected extrinsic and intrinsic pathways through, reduced expression of Bcl-2, Mcl-1, and TCTP; increased levels of the apoptotic proteins TNF-α, Fas, FADD, and Bax; and activation of cleaved caspase-3 and PARP. UA also inhibited the p-Akt and p38 MAPK signaling transduction pathways, and increased activity in the p-ERK signaling pathway. Taken together, UA inhibited the cell growth of Huh-7 cells and affected apoptosis, via regulated cellular signaling transduction.

摘要

熊果酸(UA)是一种具有广泛生物学特性的三萜酸。本文报道了 UA 对人肝癌 Huh-7 细胞凋亡和增殖的影响。MTT 结果表明,细胞活力呈浓度和时间依赖性降低。此外,还使用 DAPI 染色检测核染色质的凝聚。使用 Annexin V/PI 染色检测凋亡细胞群体。结果表明,UA 通过降低 Bcl-2、Mcl-1 和 TCTP 的表达,以及增加 TNF-α、Fas、FADD 和 Bax 等凋亡蛋白的水平,影响外源性和内源性途径,从而影响细胞凋亡。同时,UA 还抑制了 p-Akt 和 p38 MAPK 信号转导通路,并激活了 cleaved caspase-3 和 PARP。UA 还抑制了 Huh-7 细胞的细胞生长并影响凋亡,通过调节细胞信号转导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/8a10c357f52c/molecules-23-02016-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/aba35d22b61e/molecules-23-02016-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/5c9429e1e8e4/molecules-23-02016-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/e7443aeeb436/molecules-23-02016-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/5684c50fd261/molecules-23-02016-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/a2dd1fa8ddc0/molecules-23-02016-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/3261eba77428/molecules-23-02016-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/264024802da6/molecules-23-02016-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/67248378ea87/molecules-23-02016-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/8a10c357f52c/molecules-23-02016-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/aba35d22b61e/molecules-23-02016-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/5c9429e1e8e4/molecules-23-02016-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/e7443aeeb436/molecules-23-02016-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/5684c50fd261/molecules-23-02016-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/a2dd1fa8ddc0/molecules-23-02016-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/3261eba77428/molecules-23-02016-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/264024802da6/molecules-23-02016-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/67248378ea87/molecules-23-02016-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d3/6222435/8a10c357f52c/molecules-23-02016-g009.jpg

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