2017
DOI: 10.21037/hbsn.2017.06.03
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Patient-derived xenografts, a multi-faceted in vivo model enlightening research on rare liver cancer biology

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Cited by 7 publications
(5 citation statements)
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References 11 publications
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“…This allows for joint comparison of drug response between healthy and tumor organoid from the same patient and broadens the prediction path for personalized therapy [64; 66]. Another important point is that tumor organoids produced from patient is more cost-effective compared to patient-derived xenograft (PDX) models, as they require less resources and time [67]. Besides these advantages of organoids, it has the limitation of lack of communication between organs found in complex in vivo systems.…”
Section: Patient-originated Tumor Organoidsmentioning
confidence: 99%
“…This allows for joint comparison of drug response between healthy and tumor organoid from the same patient and broadens the prediction path for personalized therapy [64; 66]. Another important point is that tumor organoids produced from patient is more cost-effective compared to patient-derived xenograft (PDX) models, as they require less resources and time [67]. Besides these advantages of organoids, it has the limitation of lack of communication between organs found in complex in vivo systems.…”
Section: Patient-originated Tumor Organoidsmentioning
confidence: 99%
“…Rare cancer malignancies, such as pediatric liver cancer, have attracted the interest in developing avatar mice models for hepatoblastoma research [180,181]. Nicolle et al have studied this condition and have developed 24 tumor derived xenografts from 20 hepatoblastomas, one hepatocellular carcinoma, two malignant rhabdoid tumors, and one transitional liver cell tumor.…”
Section: Patient Derived Xenograft Modelsmentioning
confidence: 99%
“…Sublethal irradiation of other immunodeficient strains prior to cell implantation (human hematopoietic stem cells from bone marrow or umbilical cord [201] or cord-blood mononuclear cells [180]) is also preferred in obtaining humanized versions of mouse models. Then, usually after a month, tumor cell lines are implanted to study and to test different immunotherapies.…”
Section: Humanized Mice Modelsmentioning
confidence: 99%
“…They mimic the biological characteristics of the primary tumors better than do cancer cell lines. Although PDX models can better predict drug responses, their application in medicine is limited because they are expensive and time- and resource-consuming [ 4 ]. It is necessary to develop a new model that has the advantages of the two models mentioned above.…”
mentioning
confidence: 99%