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Establishment and characterization of patient-derived tumor xenograft using gastroscopic biopsies in gastric cancer

The patient-derived tumor xenograft (PDTX) model has become the most realistic model for preclinical studies. PDTX models of gastric cancer using surgical tissues are reported occasionally; however, the PDTX models using gastroscopic biopsies, which are best for evaluating new drugs, are unreported....

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Autores principales: Zhu, Yan, Tian, Tiantian, Li, Zhongwu, Tang, Zhiyu, Wang, Lai, Wu, Jian, Li, Yilin, Dong, Bin, Li, Yanyan, Li, Na, Zou, Jianling, Gao, Jing, Shen, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339807/
https://www.ncbi.nlm.nih.gov/pubmed/25712750
http://dx.doi.org/10.1038/srep08542
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author Zhu, Yan
Tian, Tiantian
Li, Zhongwu
Tang, Zhiyu
Wang, Lai
Wu, Jian
Li, Yilin
Dong, Bin
Li, Yanyan
Li, Na
Zou, Jianling
Gao, Jing
Shen, Lin
author_facet Zhu, Yan
Tian, Tiantian
Li, Zhongwu
Tang, Zhiyu
Wang, Lai
Wu, Jian
Li, Yilin
Dong, Bin
Li, Yanyan
Li, Na
Zou, Jianling
Gao, Jing
Shen, Lin
author_sort Zhu, Yan
collection PubMed
description The patient-derived tumor xenograft (PDTX) model has become the most realistic model for preclinical studies. PDTX models of gastric cancer using surgical tissues are reported occasionally; however, the PDTX models using gastroscopic biopsies, which are best for evaluating new drugs, are unreported. In our study, a total of 185 fresh gastroscopic biopsies of gastric cancer were subcutaneously transplanted into NOD/SCID (Nonobese Diabetic/Severe Combined Immunodeficiency) mice. Sixty-three PDTX models were successfully established (34.1%, 63/185) and passaged to maintain tumors in vivo, and the mean latency period of xenografts was 65.86 ± 32.84 days (11–160 days). Biopsies of prior chemotherapy had a higher transplantation rate (52.1%, 37/71) than biopsies after chemotherapy (21.9%, 25/114; P = 0.000). No differences were found between the latency period of xenografts and characteristics of patients. The pathological and molecular features of PDTX as well as chemosensitivity were highly consistent with those of primary tumors of patients. The genetic characteristics were stable during passaging of PDTX models. In summary PDTX models using gastroscopic biopsies in gastric cancer were demonstrated for the first time, and the biological characteristics of the PDTX models were highly consistent with patients, which provided the best preclinical study platform for gastric cancer.
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spelling pubmed-43398072015-03-04 Establishment and characterization of patient-derived tumor xenograft using gastroscopic biopsies in gastric cancer Zhu, Yan Tian, Tiantian Li, Zhongwu Tang, Zhiyu Wang, Lai Wu, Jian Li, Yilin Dong, Bin Li, Yanyan Li, Na Zou, Jianling Gao, Jing Shen, Lin Sci Rep Article The patient-derived tumor xenograft (PDTX) model has become the most realistic model for preclinical studies. PDTX models of gastric cancer using surgical tissues are reported occasionally; however, the PDTX models using gastroscopic biopsies, which are best for evaluating new drugs, are unreported. In our study, a total of 185 fresh gastroscopic biopsies of gastric cancer were subcutaneously transplanted into NOD/SCID (Nonobese Diabetic/Severe Combined Immunodeficiency) mice. Sixty-three PDTX models were successfully established (34.1%, 63/185) and passaged to maintain tumors in vivo, and the mean latency period of xenografts was 65.86 ± 32.84 days (11–160 days). Biopsies of prior chemotherapy had a higher transplantation rate (52.1%, 37/71) than biopsies after chemotherapy (21.9%, 25/114; P = 0.000). No differences were found between the latency period of xenografts and characteristics of patients. The pathological and molecular features of PDTX as well as chemosensitivity were highly consistent with those of primary tumors of patients. The genetic characteristics were stable during passaging of PDTX models. In summary PDTX models using gastroscopic biopsies in gastric cancer were demonstrated for the first time, and the biological characteristics of the PDTX models were highly consistent with patients, which provided the best preclinical study platform for gastric cancer. Nature Publishing Group 2015-02-25 /pmc/articles/PMC4339807/ /pubmed/25712750 http://dx.doi.org/10.1038/srep08542 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhu, Yan
Tian, Tiantian
Li, Zhongwu
Tang, Zhiyu
Wang, Lai
Wu, Jian
Li, Yilin
Dong, Bin
Li, Yanyan
Li, Na
Zou, Jianling
Gao, Jing
Shen, Lin
Establishment and characterization of patient-derived tumor xenograft using gastroscopic biopsies in gastric cancer
title Establishment and characterization of patient-derived tumor xenograft using gastroscopic biopsies in gastric cancer
title_full Establishment and characterization of patient-derived tumor xenograft using gastroscopic biopsies in gastric cancer
title_fullStr Establishment and characterization of patient-derived tumor xenograft using gastroscopic biopsies in gastric cancer
title_full_unstemmed Establishment and characterization of patient-derived tumor xenograft using gastroscopic biopsies in gastric cancer
title_short Establishment and characterization of patient-derived tumor xenograft using gastroscopic biopsies in gastric cancer
title_sort establishment and characterization of patient-derived tumor xenograft using gastroscopic biopsies in gastric cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339807/
https://www.ncbi.nlm.nih.gov/pubmed/25712750
http://dx.doi.org/10.1038/srep08542
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