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DHOK通过抑制自噬对结直肠癌发挥抗癌作用。

DHOK Exerts Anti-Cancer Effect Through Autophagy Inhibition in Colorectal Cancer.

作者信息

Shu Yuhan, Sun Xin, Ye Guiqin, Xu Mengting, Wu Zhipan, Wu Caixia, Li Shouxin, Tian Jingkui, Han Haote, Zhang Jianbin

机构信息

College of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou, China.

Department of Oncology, Cancer Center, Key Laboratory of Tumor Molecular Diagnosis and Individualized Medicine of Zhejiang Province, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China.

出版信息

Front Cell Dev Biol. 2021 Dec 17;9:760022. doi: 10.3389/fcell.2021.760022. eCollection 2021.

Abstract

DHOK (14,15β-dihydroxyklaineanone) is a novel diterpene isolated from roots of , a traditional herb widely applied in Southeast Asia. It is reported that DHOK has cytotoxic effect on cancer cells, but its anti-cancer mechanism has still been not clear. In our study, we first observed that DHOK inhibits cell proliferation of colorectal cancer cells in a time- and dose-dependent manner. Next, we performed transcriptome sequencing to identify the targets of DHOK and found that autophagy-related signaling pathways are involved under DHOK treatment. Indeed, in DHOK-treated cells, the level of autophagosome marker LC3 and the formation of GFP-LC3 puncta were decreased, indicating the reduction of autophagy. Moreover, confocal microscopy results revealed the lysosomal activity and the formation of autolysosomes are also inhibited. Our western blotting results demonstrated the activation of mammalian target of rapamycin (mTOR) signaling pathway by DHOK, which may be attributed to the enhancement of ERK and AKT activity. Functionally, activation of autophagy attenuated DHOK-caused cell death, indicating that autophagy serves as cell survival. In xenograft mouse model, our results also showed that DHOK activates the mTOR signaling pathway, decreases autophagy level and inhibits the tumorigenesis of colon cancer. Taken together, we revealed the molecular mechanism of DHOK against cancer and our results also demonstrate great potential of DHOK in the treatment of colorectal cancer.

摘要

DHOK(14,15β-二羟基克莱因酮)是从一种在东南亚广泛应用的传统草药的根中分离出的新型二萜。据报道,DHOK对癌细胞具有细胞毒性作用,但其抗癌机制仍不清楚。在我们的研究中,我们首先观察到DHOK以时间和剂量依赖性方式抑制结肠癌细胞的增殖。接下来,我们进行了转录组测序以鉴定DHOK的靶点,并发现自噬相关信号通路在DHOK处理下被涉及。实际上,在DHOK处理的细胞中,自噬体标志物LC3的水平和GFP-LC3斑点的形成减少,表明自噬减少。此外,共聚焦显微镜结果显示溶酶体活性和自噬溶酶体的形成也受到抑制。我们的蛋白质印迹结果证明DHOK激活了雷帕霉素哺乳动物靶标(mTOR)信号通路,这可能归因于ERK和AKT活性的增强。在功能上,自噬的激活减弱了DHOK引起的细胞死亡,表明自噬起到细胞存活的作用。在异种移植小鼠模型中,我们的结果还表明DHOK激活mTOR信号通路,降低自噬水平并抑制结肠癌的肿瘤发生。综上所述,我们揭示了DHOK抗癌的分子机制,我们的结果也证明了DHOK在治疗结肠癌方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d7/8719673/4aab57e48485/fcell-09-760022-g001.jpg

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