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

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作者
Francesca Maradonna
Camilla M. Fontana
Fiorenza Sella
Christian Giommi
Nicola Facchinello
Chiara Rampazzo
Micol Caichiolo
Seyed Hossein Hoseinifar
Luisa Dalla Valle
Hien Van Doan
Oliana Carnevali
机构
[1] Polytechnic University of Marche,Department of Life and Environmental Sciences
[2] Biostructures and Biosystems National Institute,Department of Animal and Aquatic Sciences, Faculty of Agriculture
[3] (INBB),Department of Molecular Medicine
[4] Chiang Mai University,Department of Biology
[5] National Research Council (CNR),Department of Fisheries, Faculty of Fisheries and Environmental Sciences
[6] Neuroscience Institute,undefined
[7] University of Padova,undefined
[8] University of Padova,undefined
[9] Gorgan University of Agricultural Sciences and Natural Resources,undefined
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摘要
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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