Chick chorioallantoic membrane assay as an in vivo model to study the effect of nanoparticle-based anticancer drugs in ovarian cancer

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作者
Binh Thanh Vu
Sophia Allaf Shahin
Jonas Croissant
Yevhen Fatieiev
Kotaro Matsumoto
Tan Le-Hoang Doan
Tammy Yik
Shirleen Simargi
Altagracia Conteras
Laura Ratliff
Chiara Mauriello Jimenez
Laurence Raehm
Niveen Khashab
Jean-Olivier Durand
Carlotta Glackin
Fuyuhiko Tamanoi
机构
[1] University of California,Department of Microbiology, Immunology and Molecular Genetics, Jonsson Comprehensive Cancer Center
[2] City of Hope-Beckman Research Institute,Department of Developmental and Stem Cell Biology
[3] King Abdullah University of Science and Technology,Smart Hybrid Materials Laboratory (SHMs)
[4] Kyoto University,Institute for Integrated Cell
[5] Institut Charles Gerhardt Montpellier,Material Sciences, Institute for Advanced Study
[6] UMR-5253 CNRS-UM2-ENSCM-UM1,Laboratory for Stem Cell Research and Application
[7] Vietnam National University-Ho Chi Minh City,Center for Micro
[8] University of New Mexico,Engineered Materials, Advanced Materials Laboratory
[9] Vietnam National University-Ho Chi Minh City,Center for Innovative Materials and Architectures
来源
Scientific Reports | / 8卷
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摘要
New therapy development is critically needed for ovarian cancer. We used the chicken egg CAM assay to evaluate efficacy of anticancer drug delivery using recently developed biodegradable PMO (periodic mesoporous organosilica) nanoparticles. Human ovarian cancer cells were transplanted onto the CAM membrane of fertilized eggs, resulting in rapid tumor formation. The tumor closely resembles cancer patient tumor and contains extracellular matrix as well as stromal cells and extensive vasculature. PMO nanoparticles loaded with doxorubicin were injected intravenously into the chicken egg resulting in elimination of the tumor. No significant damage to various organs in the chicken embryo occurred. In contrast, injection of free doxorubicin caused widespread organ damage, even when less amount was administered. The lack of toxic effect of nanoparticle loaded doxorubicin was associated with specific delivery of doxorubicin to the tumor. Furthermore, we observed excellent tumor accumulation of the nanoparticles. Lastly, a tumor could be established in the egg using tumor samples from ovarian cancer patients and that our nanoparticles were effective in eliminating the tumor. These results point to the remarkable efficacy of our nanoparticle based drug delivery system and suggests the value of the chicken egg tumor model for testing novel therapies for ovarian cancer.
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