A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer

血管生成 阿那达胺 大麻素受体 AM251型 斑马鱼 细胞生长 癌症研究 内大麻素系统 生物 癌症 化学 细胞生物学 药理学 受体 敌手 生物化学 基因 遗传学
作者
Francesca Maradonna,Camilla Maria Fontana,Fiorenza Sella,Christian Giommi,Nicola Facchinello,Chiara Rampazzo,Micol Caichiolo,Seyed Hossein Hoseinifar,Luisa Dalla Valle,Hien Van Doan,Oliana Carnevali
出处
期刊:Cell Death and Disease [Springer Nature]
卷期号:13 (12) 被引量:3
标识
DOI:10.1038/s41419-022-05523-z
摘要

Abstract Colon cancer is one of the leading causes of death worldwide. In recent years, cannabinoids have been extensively studied for their potential anticancer effects and symptom management. Several in vitro studies reported anandamide’s (AEA) ability to block cancer cell proliferation and migration, but evidence from in vivo studies is still lacking. Thus, in this study, the effects of AEA exposure in zebrafish embryos transplanted with HCT116 cells were evaluated. Totally, 48 hpf xenografts were exposed to 10 nM AEA, 10 nM AM251, one of the cannabinoid 1 receptor (CB1) antagonist/inverse agonists, and to AEA + AM251, to verify the specific effect of AEA treatment. AEA efficacy was evaluated by confocal microscopy, which demonstrated that these xenografts presented a smaller tumor size, reduced tumor angiogenesis, and lacked micrometastasis formation. To gain deeper evidence into AEA action, microscopic observations were completed by molecular analyses. RNA seq performed on zebrafish transcriptome reported the downregulation of genes involved in cell proliferation, angiogenesis, and the immune system. Conversely, HCT116 cell transcripts resulted not affected by AEA treatment. In vitro HCT116 culture, in fact, confirmed that AEA exposure did not affect cell proliferation and viability, thus suggesting that the reduced tumor size mainly depends on direct effects on the fish rather than on the transplanted cancer cells. AEA reduced cell proliferation and tumor angiogenesis, as suggested by socs3 and pcnp mRNAs and Vegfc protein levels, and exerted anti-inflammatory activity, as indicated by the reduction of il-11a , mhc1uba , and csf3b mRNA. Of note, are the results obtained in groups exposed to AM251, which presence nullifies AEA’s beneficial effects. In conclusion, this study promotes the efficacy of AEA in personalized cancer therapy, as suggested by its ability to drive tumor growth and metastasis, and strongly supports the use of zebrafish xenograft as an emerging model platform for cancer studies.
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