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Establishment and evaluation of four different types of patient-derived xenograft models.
Ji, Xiaoqian; Chen, Siyu; Guo, Yanwu; Li, Wende; Qi, Xiaolong; Yang, Han; Xiao, Sa; Fang, Guang; Hu, Jinfang; Wen, Chuangyu; Liu, Huanliang; Han, Zhen; Deng, Guangxu; Yang, Qingbin; Yang, Xiangling; Xu, Yuting; Peng, Zhihong; Li, Fengping; Cai, Nvlue; Li, Guoxin; Huang, Ren.
Afiliação
  • Ji X; School of Basic Courses, Guangdong Pharmaceutical University, Guangzhou, 510006 China.
  • Chen S; Guangdong Laboratory Animals Monitoring Institute, Guangdong Key Laboratory Animal Lab, 11 Fengxin Road, Science City, Guangzhou, 510663 China.
  • Guo Y; Guangdong Laboratory Animals Monitoring Institute, Guangdong Key Laboratory Animal Lab, 11 Fengxin Road, Science City, Guangzhou, 510663 China.
  • Li W; Department of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510282 China.
  • Qi X; Guangdong Laboratory Animals Monitoring Institute, Guangdong Key Laboratory Animal Lab, 11 Fengxin Road, Science City, Guangzhou, 510663 China.
  • Yang H; Department of General Surgery, Nanfang Hospital, Southern Medical University, 1838 Baiyun Road North, Guangzhou, 510080 China.
  • Xiao S; Department of Thoracic Surgery, Sun Yat-Sen University Cancer Center, Guangzhou, 510030 China.
  • Fang G; Guangdong Laboratory Animals Monitoring Institute, Guangdong Key Laboratory Animal Lab, 11 Fengxin Road, Science City, Guangzhou, 510663 China.
  • Hu J; Guangdong Key Laboratory for Research and Development of Natural Drug, Guangdong Medical University, Zhanjiang, 524003 Guangdong China.
  • Wen C; Guangdong Laboratory Animals Monitoring Institute, Guangdong Key Laboratory Animal Lab, 11 Fengxin Road, Science City, Guangzhou, 510663 China.
  • Liu H; Guangdong Key Laboratory for Research and Development of Natural Drug, Guangdong Medical University, Zhanjiang, 524003 Guangdong China.
  • Han Z; Guangdong Laboratory Animals Monitoring Institute, Guangdong Key Laboratory Animal Lab, 11 Fengxin Road, Science City, Guangzhou, 510663 China.
  • Deng G; Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology and the Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510150 China.
  • Yang Q; Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology and the Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510150 China.
  • Yang X; Department of General Surgery, Nanfang Hospital, Southern Medical University, 1838 Baiyun Road North, Guangzhou, 510080 China.
  • Xu Y; Department of General Surgery, Nanfang Hospital, Southern Medical University, 1838 Baiyun Road North, Guangzhou, 510080 China.
  • Peng Z; Department of General Surgery, Nanfang Hospital, Southern Medical University, 1838 Baiyun Road North, Guangzhou, 510080 China.
  • Li F; Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology and the Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510150 China.
  • Cai N; Department of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510282 China.
  • Li G; Guangdong Laboratory Animals Monitoring Institute, Guangdong Key Laboratory Animal Lab, 11 Fengxin Road, Science City, Guangzhou, 510663 China.
  • Huang R; Guangdong Key Laboratory for Research and Development of Natural Drug, Guangdong Medical University, Zhanjiang, 524003 Guangdong China.
Cancer Cell Int ; 17: 122, 2017.
Article em En | MEDLINE | ID: mdl-29296105
ABSTRACT

BACKGROUND:

Patient-derived xenografts (PDX) have a biologically stable in tumor architecture, drug responsiveness, mutational status and global gene-expression patterns. Numerous PDX models have been established to date, however their thorough characterization regarding the tumor formation and rates of tumor growth in the established models remains a challenging task. Our study aimed to provide more detailed information for establishing the PDX models successfully and effectively.

METHODS:

We transplanted four different types of solid tumors from 108 Chinese patients, including 21 glioblastoma (GBM), 11 lung cancers (LC), 54 gastric cancers (GC) and 21 colorectal cancers (CRC), and took tumor tissues passaged for three successive generations. Here we report the rate of tumor formation, tumor-forming times, tumor growth curves and mortality of mice in PDX model. We also report H&E staining and immunohistochemistry for HLA-A, CD45, Ki67, GFAP, and CEA protein expression between patient cancer tissues and PDX models.

RESULTS:

Tumor formation rate increased significantly in subsequent tumor generations. Also, the survival rates of GC and CRC were remarkably higher than GBM and LC. As for the time required for the formation of tumors, which reflects the tumor growth rate, indicated that tumor growth rate always increased as the generation number increased. The tumor growth curves also illustrate this law. Similarly, the survival rate of PDX mice gradually improved with the increased generation number in GC and CRC. And generally, there was more proliferation (Ki67+) in the PDX models than in the patient tumors, which was in accordance with the results of tumor growth rate. The histological findings confirm similar histological architecture and degrees of differentiation between patient cancer tissues and PDX models with statistical analysis by GraphPad Prism 5.0.

CONCLUSION:

We established four different types of PDX models successfully, and our results add to the current understanding of the establishment of PDX models and may contribute to the extension of application of different types of PDX models.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Cancer Cell Int Ano de publicação: 2017 Tipo de documento: Article País de publicação: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Cancer Cell Int Ano de publicação: 2017 Tipo de documento: Article País de publicação: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM