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山柰酚通过 NAG-1 信号诱导细胞凋亡在胃癌中的潜在治疗作用。

Potential Therapeutic Role of Hispidulin in Gastric Cancer through Induction of Apoptosis via NAG-1 Signaling.

机构信息

Department of Biotechnology and Animal Science, College of Bioresources, National Ilan University, Ilan 260, Taiwan.

出版信息

Evid Based Complement Alternat Med. 2013;2013:518301. doi: 10.1155/2013/518301. Epub 2013 Sep 15.

DOI:10.1155/2013/518301
PMID:24159347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3789485/
Abstract

Gastric cancer is one of the most common malignant cancers due to poor prognoses and high mortality rates worldwide. However, an effective chemotherapeutic drug without side effects remains lacking. Saussurea involucrata (SI) Kar. et Kir., also known as snow lotus, grows in mountainous rocky habitats at 2600 m elevation in the Tian Shan and A'er Tai regions of China. The ethyl acetate extract of SI had been shown to inhibit proliferation and induce apoptosis in various tumor cells. In this study, we demonstrated that Hispidulin, active ingredients in SI, inhibits the growth of AGS gastric cancer cells. After Hispidulin treatment, NAG-1 remained highly expressed, whereas COX-2 expression was downregulated. Flow cytometric analysis indicated that Hispidulin induces G1/S phase arrest and apoptosis in time- and concentration-dependent manners. G1/S arrest correlated with upregulated p21/WAF1 and p16 and downregulated cyclin D1 and cyclin E, independent of p53 pathway. In addition, Hispidulin can elevate Egr-1 expression and ERK1/2 activity, whereas ERK1/2 inhibitor markedly attenuated NAG-1 mediated apoptosis. Taken together, Hispidulin can efficiently activate ERK1/2 signaling followed by NAG-1 constitutive expression and trigger cell cycle arrest as well as apoptosis in cancer cell. It can be a potential compound for combination therapy of gastric cancer in the future.

摘要

胃癌是世界范围内预后差和死亡率高的最常见恶性肿瘤之一。然而,仍然缺乏一种没有副作用的有效化疗药物。雪莲(SI)Kar.et Kir.,又称雪莲花,生长在中国天山和阿尔泰地区海拔 2600 米的山区岩石栖息地。SI 的乙酸乙酯提取物已被证明能抑制各种肿瘤细胞的增殖并诱导其凋亡。在这项研究中,我们证明雪莲中的活性成分虎耳草素能抑制 AGS 胃癌细胞的生长。在虎耳草素处理后,NAG-1 保持高表达,而 COX-2 表达下调。流式细胞术分析表明,虎耳草素能以时间和浓度依赖的方式诱导 G1/S 期阻滞和细胞凋亡。G1/S 阻滞与 p21/WAF1 和 p16 的上调以及 cyclin D1 和 cyclin E 的下调相关,与 p53 途径无关。此外,虎耳草素能上调 Egr-1 表达和 ERK1/2 活性,而 ERK1/2 抑制剂则显著减弱了 NAG-1 介导的凋亡。总之,虎耳草素能有效地激活 ERK1/2 信号通路,随后 NAG-1 组成性表达,并引发细胞周期阻滞和癌细胞凋亡。它可能是未来胃癌联合治疗的一种潜在化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/0f218de51de7/ECAM2013-518301.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/f724d0f6efd0/ECAM2013-518301.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/e532d0c79c9b/ECAM2013-518301.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/727334935940/ECAM2013-518301.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/6e17d5e15611/ECAM2013-518301.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/2804167ec75c/ECAM2013-518301.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/0f218de51de7/ECAM2013-518301.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/f724d0f6efd0/ECAM2013-518301.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/e532d0c79c9b/ECAM2013-518301.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/727334935940/ECAM2013-518301.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/6e17d5e15611/ECAM2013-518301.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/2804167ec75c/ECAM2013-518301.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e6a/3789485/0f218de51de7/ECAM2013-518301.006.jpg

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