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二萜类丹参酮通过内质网应激介导的凋亡信号通路的抗肺癌机制

[Anti-lung cancer mechanisms of diterpenoid tanshinone via endoplasmic reticulum stress-mediated apoptosis signal pathway].

作者信息

Lou Zhao-Huan, Xia Rong-Man, Li Xiao-Juan, Cheng Ru-Bin, Shao Ke-Ding, Zhang Guang-Ji

机构信息

Zhejiang Chinese Medical University, Hangzhou 310053, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2018 Dec;43(24):4900-4907. doi: 10.19540/j.cnki.cjcmm.20180725.002.

Abstract

At present, lung cancer ranks second and first respectively in the incidence and the mortality among malignant tumors. It is urgent to find new effective anti-lung cancer drugs with less side effects and relatively defined mechanisms. Endoplasmic reticulum stress (ERS)-mediated apoptosis pathway is an effective way to promote tumor cell apoptosis; diterpenoid tanshinone (DT), an effective part separated from Salviae Miltiorrhizae Radix et Rhizoma, was found to have an anti-lung cancer effect in previous studies via ERS-induced PERK-EIF2α pathway. In this paper, human lung adenocarcinoma PC9 cell line and nude mouse transplantation tumor model were applied to verify the anti-lung cancer effect of DT in vivo and in vitro, and illuminate the potential mechanism via ERS induced IRE1α/caspase 12 apoptosis pathway. The results showed that in vivo, DT could promote PC9 cell apoptosis in a concentration-dependent manner, up-regulate Bip, IRE1 and TRAF2 protein expressions in tumor tissue, reduce tumor weight and alleviate bodyweight loss. In vitro, DT inhibited the proliferation of PC9 cell line in a concentration-dependent manner, and destroyed the structure of mitochondria in PC9 cell, promoted Bax, IRE1α, Bip, TRAF2 and caspase 12 protein expressions, lower Bcl-2 protein expression in a time-dependent manner. DT shows a good effect on anti-lung cancer both in vivo and in vitro. The mechanism is related to the activation of ERS-induced IRE1α/caspase 12 apoptosis pathway and the promotion of cell apoptosis. ERS-mediated apoptosis pathway may be an important target of DT on anti-lung cancer.

摘要

目前,肺癌在恶性肿瘤的发病率和死亡率中分别位居第二和第一。迫切需要寻找新的、副作用较小且作用机制相对明确的有效抗肺癌药物。内质网应激(ERS)介导的凋亡途径是促进肿瘤细胞凋亡的有效方式;二萜类丹参酮(DT)是从丹参中分离出的有效成分,前期研究发现其可通过ERS诱导的PERK-EIF2α途径发挥抗肺癌作用。本文应用人肺腺癌PC9细胞系和裸鼠移植瘤模型,验证DT在体内外的抗肺癌作用,并阐明其通过ERS诱导的IRE1α/caspase 12凋亡途径发挥作用的潜在机制。结果显示,在体内,DT可呈浓度依赖性促进PC9细胞凋亡,上调肿瘤组织中Bip、IRE1和TRAF2蛋白表达,减轻肿瘤重量并缓解体重下降。在体外,DT呈浓度依赖性抑制PC9细胞系增殖,破坏PC9细胞线粒体结构,呈时间依赖性促进Bax、IRE1αBip TRAF2和caspase 12蛋白表达,降低Bcl-2蛋白表达。DT在体内外均显示出良好的抗肺癌效果。其机制与激活ERS诱导的IRE1α/caspase 12凋亡途径及促进细胞凋亡有关。ERS介导的凋亡途径可能是DT抗肺癌的重要靶点。

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