Department of Pharmacology, School of Pharmacy, Qingdao University, Qingdao 266021, China.
School of Basic Medicine, Qingdao University, Qingdao 266021, China.
Life Sci. 2020 Sep 15;257:118065. doi: 10.1016/j.lfs.2020.118065. Epub 2020 Jul 11.
Pyroptosis is a newly discovered inflammatory programmed cell death. This study was to investigate whether pyroptosis is involved in the anti-colorectal cancer process of FL118.
The relationship between NLRP3 and caspase-1 and colorectal cancer was analyzed by bioinformatics. MTT was used to detect the cell viability. Cell membrane integrity was examined by LDH release. Wound healing assay and Transwell were used to detect the cell migration and invasion respectively. TUNEL was to check the cell death. The expression of pyroptosis-related factors was detected using qRT-PCR, Western blotting, Immunofluorescence and Elisa. And H&E staining was used to detect the toxicity of FL118 in colorectal cancer.
In vitro, FL118 significantly inhibited the proliferation, migration and invasion of colorectal cancer, and the morphological characteristics of pyroptosis were observed under the microscope. With the change of FL118 concentration, the release rate of LDH in the supernatant and the expression of pyroptosis-related factors emerged an increase. However, pyroptosis induced by FL118 was reversed with the participation of MCC950 and VX-765, which suppressed the antitumor effect of FL118. In vivo, the result in the xenograft animal model and lung metastasis model experimental showed that FL118 could activate pyroptosis and thus inhibit the metastasis of colorectal cancer.
FL118 restrains the growth and metastasis of colorectal cancer by inducing NLRP3-ASC-Caspase-1 mediated pyroptosis, which provides important evidence in the study on the role of pyroptosis and different tumors.
细胞焦亡是一种新发现的炎症程序性细胞死亡。本研究旨在探讨细胞焦亡是否参与 FL118 的抗结直肠癌过程。
通过生物信息学分析 NLRP3 与 caspase-1 与结直肠癌的关系。MTT 法检测细胞活力。LDH 释放检测细胞膜完整性。划痕愈合实验和 Transwell 分别检测细胞迁移和侵袭。TUNEL 检测细胞死亡。采用 qRT-PCR、Western blot、免疫荧光和 Elisa 检测细胞焦亡相关因子的表达。并用 H&E 染色检测 FL118 对结直肠癌的毒性。
体外,FL118 显著抑制结直肠癌细胞的增殖、迁移和侵袭,并在显微镜下观察到细胞焦亡的形态特征。随着 FL118 浓度的变化,上清液中 LDH 的释放率和细胞焦亡相关因子的表达呈上升趋势。然而,MCC950 和 VX-765 的参与逆转了 FL118 诱导的细胞焦亡,抑制了 FL118 的抗肿瘤作用。体内,在异种移植动物模型和肺转移模型实验中的结果表明,FL118 可以通过激活细胞焦亡从而抑制结直肠癌的转移。
FL118 通过诱导 NLRP3-ASC-Caspase-1 介导的细胞焦亡来抑制结直肠癌细胞的生长和转移,为研究细胞焦亡与不同肿瘤的作用提供了重要依据。