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来自日本花椒的花椒果实提取物可促进癌细胞的自噬性细胞死亡。

Zanthoxylum fruit extract from Japanese pepper promotes autophagic cell death in cancer cells.

作者信息

Nozaki Reo, Kono Toru, Bochimoto Hiroki, Watanabe Tsuyoshi, Oketani Kaori, Sakamaki Yuichi, Okubo Naoto, Nakagawa Koji, Takeda Hiroshi

机构信息

Pathophysiology and Therapeutics, Hokkaido University Faculty of Pharmaceutical Sciences, Sapporo, Hokkaido, Japan.

Center for Clinical and Biomedical Research, Sapporo Higashi-Tokushukai Hospital, Sapporo, Hokkaido, Japan.

出版信息

Oncotarget. 2016 Oct 25;7(43):70437-70446. doi: 10.18632/oncotarget.11926.

Abstract

Zanthoxylum fruit, obtained from the Japanese pepper plant (Zanthoxylum piperitum De Candolle), and its extract (Zanthoxylum fruit extract, ZFE) have multiple physiological activities (e.g., antiviral activity). However, the potential anticancer activity of ZFE has not been fully examined. In this study, we investigated the ability of ZFE to induce autophagic cell death (ACD). ZFE caused remarkable autophagy-like cytoplasmic vacuolization, inhibited cell proliferation, and ultimately induced cell death in the human cancer cell lines DLD-1, HepG2, and Caco-2, but not in A549, MCF-7, or WiDr cells. ZFE increased the level of LC3-II protein, a marker of autophagy. Knockdown of ATG5 using siRNA inhibited ZFE-induced cytoplasmic vacuolization and cell death. Moreover, in cancer cells that could be induced to undergo cell death by ZFE, the extract increased the phosphorylation of c-Jun N-terminal kinase (JNK), and the JNK inhibitor SP600125 attenuated both vacuolization and cell death. Based on morphology and expression of marker proteins, ZFE-induced cell death was neither apoptosis nor necrosis. Normal intestinal cells were not affected by ZFE. Taken together, our findings show that ZFE induces JNK-dependent ACD, which appears to be the main mechanism underlying its anticancer activity, suggesting a promising starting point for anticancer drug development.

摘要

花椒果实取自日本花椒植物(花椒,德堪多),其提取物(花椒果实提取物,ZFE)具有多种生理活性(如抗病毒活性)。然而,ZFE的潜在抗癌活性尚未得到充分研究。在本研究中,我们调查了ZFE诱导自噬性细胞死亡(ACD)的能力。ZFE在人癌细胞系DLD-1、HepG2和Caco-2中引起显著的自噬样细胞质空泡化,抑制细胞增殖,并最终诱导细胞死亡,但在A549、MCF-7或WiDr细胞中未出现这种情况。ZFE增加了自噬标志物LC3-II蛋白的水平。使用小干扰RNA敲低ATG5可抑制ZFE诱导的细胞质空泡化和细胞死亡。此外,在可被ZFE诱导发生细胞死亡的癌细胞中,该提取物增加了c-Jun氨基末端激酶(JNK)的磷酸化,而JNK抑制剂SP600125可减弱空泡化和细胞死亡。基于标志物蛋白的形态和表达,ZFE诱导的细胞死亡既不是凋亡也不是坏死。正常肠细胞不受ZFE影响。综上所述,我们的研究结果表明,ZFE诱导JNK依赖的ACD,这似乎是其抗癌活性的主要机制,为抗癌药物开发提供了一个有前景的起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ec6/5342563/9f950b7c1b9a/oncotarget-07-70437-g001.jpg

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