PUBLICATION
A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer
- Authors
- Maradonna, F., Fontana, C.M., Sella, F., Giommi, C., Facchinello, N., Rampazzo, C., Caichiolo, M., Hoseinifar, S.H., Dalla Valle, L., Van Doan, H., Carnevali, O.
- ID
- ZDB-PUB-221224-43
- Date
- 2022
- Source
- Cell Death & Disease 13: 10691069 (Journal)
- Registered Authors
- Carnevali, Oliana, Dalla Valle, Luisa, Facchinello, Nicola, Fontana, Camila Maria
- Keywords
- none
- MeSH Terms
-
- Animals
- Colorectal Neoplasms*/drug therapy
- Colorectal Neoplasms*/genetics
- Disease Models, Animal
- Drug Inverse Agonism
- Heterografts
- Humans
- Polyunsaturated Alkamides/pharmacology
- Polyunsaturated Alkamides/therapeutic use
- Receptor, Cannabinoid, CB1
- Zebrafish*
- PubMed
- 36564370 Full text @ Cell Death Dis.
Citation
Maradonna, F., Fontana, C.M., Sella, F., Giommi, C., Facchinello, N., Rampazzo, C., Caichiolo, M., Hoseinifar, S.H., Dalla Valle, L., Van Doan, H., Carnevali, O. (2022) A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer. Cell Death & Disease. 13:10691069.
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.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping