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茜素,一种天然化合物,通过阻断 NF-κB 激活来抑制胰腺癌细胞的生长。

Alizarin, a nature compound, inhibits the growth of pancreatic cancer cells by abrogating NF-κB activation.

机构信息

Shanghai Key Laboratory of Health Identification and Assessment, School of Basic Medical Science, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Department of General Surgery, Xinhua Hospital affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.

出版信息

Int J Biol Sci. 2022 Mar 28;18(7):2759-2774. doi: 10.7150/ijbs.70567. eCollection 2022.

Abstract

The current performance of nature compounds in antitumor field is gradually attracted more and more attention, we discovered a nature active ingredient alizarin possess potent natural reductive NF-κB activity to against pancreatic cancer. However, the preclinical pharmacology and therapeutic effect, and the underlying mechanisms of alizarin in inhibiting pancreatic cancer are still unclear. After high-throughput screening, this is the first report that alizarin can induce a potent inhibitory effect against pancreatic cancer cells. Alizarin induced cell cycle arrest and promoted cell apoptosis by inhibiting TNF-α-stimulated NF-κB activity and nuclear translocation, and inactivated its related TNF-α-TAK1-NF-κB signaling cascade followed by downregulation of NF-κB target genes involved in cell apoptosis (Bcl-2, Bcl-xL, XIAP) and in the cell cycle and growth (cyclin D, c-myc). Due to the abrogation of NF-κB activity, combination of alizarin and gemcitabine exerted a better inhibitory effect on pancreatic cancer. In summary, natural component alizarin, inhibited cell proliferation and induced apoptosis and through targeting of the NF-κB signaling cascade with minimal toxicity, which combine with gemcitabine, can significantly enhance the antitumor capability, playing a synergistic effect. Therefore, alizarin may play a role in reversing gemcitabine resistance caused by overactivated NF-κB in clinical application in the future.

摘要

目前,天然化合物在抗肿瘤领域的表现逐渐引起了越来越多的关注。我们发现一种天然活性成分茜素具有很强的天然还原型 NF-κB 活性,能够对抗胰腺癌。然而,茜素抑制胰腺癌的临床前药理学和治疗效果以及潜在机制仍不清楚。经过高通量筛选,这是首次报道茜素可以对胰腺癌细胞产生强烈的抑制作用。茜素通过抑制 TNF-α 刺激的 NF-κB 活性和核易位,诱导细胞周期停滞并促进细胞凋亡,从而失活其相关的 TNF-α-TAK1-NF-κB 信号级联,随后下调参与细胞凋亡(Bcl-2、Bcl-xL、XIAP)和细胞周期和生长(细胞周期蛋白 D、c-myc)的 NF-κB 靶基因。由于 NF-κB 活性的阻断,茜素与吉西他滨联合使用对胰腺癌表现出更好的抑制作用。总之,天然成分茜素通过靶向 NF-κB 信号级联抑制细胞增殖并诱导细胞凋亡,同时具有最小的毒性,与吉西他滨联合使用可以显著增强抗肿瘤能力,发挥协同作用。因此,茜素可能在未来的临床应用中在逆转由过度激活的 NF-κB 引起的吉西他滨耐药方面发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db8b/9066114/b6bc7f167202/ijbsv18p2759g001.jpg

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