Novel patient-derived xenograft and cell line models for therapeutic testing of pediatric liver cancer

被引:55
|
作者
Bissig-Choisat, Beatrice [1 ]
Kettlun-Leyton, Claudia [1 ]
Legras, Xavier D. [1 ]
Zorman, Barry [2 ]
Barzi, Mercedes [1 ]
Chen, Leon L. [1 ]
Amin, Mansi D. [1 ]
Huang, Yung-Hsin [3 ]
Pautler, Robia G. [4 ,5 ]
Hampton, Oliver A. [6 ,7 ,8 ]
Prakash, Masand M. [9 ]
Yang, Diane [1 ,15 ]
Borowiak, Malgorzata [1 ,3 ,15 ,16 ]
Muzny, Donna [6 ]
Doddapaneni, Harsha Vardhan [6 ]
Hu, Jianhong [6 ]
Shi, Yan [10 ,11 ,12 ]
Gaber, M. Waleed [2 ,4 ,8 ]
Hicks, M. John [13 ]
Thompson, Patrick A. [2 ]
Lu, Yiling [14 ]
Mills, Gordon B. [14 ]
Finegold, Milton [8 ,13 ]
Goss, John A. [10 ,11 ,12 ]
Parsons, D. Williams [2 ,6 ,7 ,8 ]
Vasudevan, Sanjeev A. [8 ,10 ,11 ,12 ]
Sumazin, Pavel [2 ,8 ]
Lopez-Terrada, Dolores [8 ,13 ]
Bissig, Karl-Dimiter [1 ,3 ,8 ,15 ]
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Stem Cells & Regenerat Med Ctr, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
[3] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
[4] Texas Childrens Hosp, Small Anim Imaging Facil, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Mol Physiol & Biophys, Houston, TX 77030 USA
[6] Baylor Coll Med, Human Genome Sequencing Ctr, Houston, TX 77030 USA
[7] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[8] Baylor Coll Med, Dan L Duncan Canc Ctr, Houston, TX 77030 USA
[9] Texas Childrens Hosp, Dept Pediat Radiol, Houston, TX 77030 USA
[10] Baylor Coll Med, Michael E DeBakey Dept Surg, Div Abdominal Transplantat, Houston, TX 77030 USA
[11] Baylor Coll Med, Div Hepatobiliary Surg, Houston, TX 77030 USA
[12] Texas Childrens Hosp, Dept Surg, Houston, TX 77030 USA
[13] Texas Childrens Hosp, Dept Pathol, Houston, TX 77030 USA
[14] Univ Texas MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77030 USA
[15] Baylor Coll Med, Grad Program, Dept Mol & Cellular Biol, Houston, TX USA
[16] McNair Med Inst, Houston, TX USA
关键词
Pediatric liver cancer; Patient-derived xenograft; Therapeutic testing; HUMAN HEPATOBLASTOMA; ORTHOTOPIC MODELS; HUMAN HEPATOCYTES; IN-VITRO; ESTABLISHMENT; TUMOR; DIFFERENTIATION; CARCINOMA; MICE; TRANSPLANTATION;
D O I
10.1016/j.jhep.2016.04.009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Pediatric liver cancer is a rare but serious disease whose incidence is rising, and for which the therapeutic options are limited. Development of more targeted, less toxic therapies is hindered by the lack of an experimental animal model that captures the heterogeneity and metastatic capability of these tumors. Methods: Here we established an orthotopic engraftment technique to model a series of patient-derived tumor xenograft (PDTX) from pediatric liver cancers of all major histologic sub-types: hepatoblastoma, hepatocellular cancer and hepatocellular malignant neoplasm. We utilized standard (immuno) staining methods for histological characterization, RNA sequencing for gene expression profiling and genome sequencing for identification of druggable targets. We also adapted stem cell culturing techniques to derive two new pediatric cancer cell lines from the xenografted mice. Results: The patient-derived tumor xenografts recapitulated the histologic, genetic, and biological characteristics-including the metastatic behavior-of the corresponding primary tumors. Furthermore, the gene expression profiles of the two new liver cancer cell lines closely resemble those of the primary tumors. Targeted therapy of PDTX from an aggressive hepatocellular malignant neoplasm with the MEK1 inhibitor trametinib and pan-class I PI3 kinase inhibitor NVP-BKM120 resulted in significant growth inhibition, thus confirming this PDTX model as a valuable tool to study tumor biology and patient-specific therapeutic responses. Conclusions: The novel metastatic xenograft model and the isogenic xenograft-derived cell lines described in this study provide reliable tools for developing mutation-and patient-specific therapies for pediatric liver cancer. Lay summary: Pediatric liver cancer is a rare but serious disease and no experimental animal model currently captures the complexity and metastatic capability of these tumors. We have established a novel animal model using human tumor tissue that recapitulates the genetic and biological characteristics of this cancer. We demonstrate that our patient-derived animal model, as well as two new cell lines, are useful tools for experimental therapies. (C) 2016 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:325 / 333
页数:9
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