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Abstract 2810: Using CRISPR/Cas9 to generate primary soft tissue sarcoma in genetically engineered and wild-type mice

Publication ,  Conference
Huang, J; Chen, M; Whitley, MJ; Kuo, H-C; Walens, A; Mowery, YM; Mater, DV; Eward, W; Cardona, DM; Luo, L; Ma, Y; Nelson, CE; Gersbach, CA ...
Published in: Cancer Research
July 1, 2017

Genetically engineered mouse models (GEMMs) that employ site-specific recombinase (SSR) technology are important tools for pre-clinical studies, but this approach is costly and time-consuming. Here, we show that the CRISPR/Cas9 system can be used to efficiently complement existing GEMMs of sarcoma and generate primary sarcomas in wild type mice. Mice with the genotype KrasLSL-G12D/+; Rosa26LSL-Cas9-EGFP/+ received intramuscular delivery of an adenovirus expressing Cre recombinase and a single guide RNA (sgRNA) targeting Trp53. Cre-mediated expression of oncogenic Kras and Cas9, in combination with CRISPR/Cas9-mediated knockout of Trp53, was sufficient to generate primary soft tissue sarcomas. These tumors arose with kinetics similar to those generated using the Cre-loxP system to activate oncogenic Kras and delete Trp53 alleles. Additionally, we injected an adenovirus containing Cas9 and sgRNAs targeting Nf1 and Trp53 into the sciatic nerve of wild type mice. These mice formed malignant peripheral nerve sheath tumors (MPNSTs) in the same timeframe as MPNSTs generated using the Cre-loxP system to delete Nf1 and Ink4a/Arf alleles in GEMMs. These data demonstrate that CRISPR/Cas9 can be used to generate soft tissue sarcomas in wild type mice. Moreover, these results suggest that this technology can complement existing GEMMs for rapid assessment of tumor-modifying genes. These tools should decrease the time and expense associated with employing autochthonous mouse models of sarcoma for preclinical research.Citation Format: Jianguo Huang, Mark Chen, Melodi J. Whitley, Hsuan-Cheng Kuo, Andrea Walens, Yvonne M. Mowery, David V. Mater, William Eward, Diana M. Cardona, Lixia Luo, Yan Ma, Christopher E. Nelson, Jacqueline N. Robinson-Hamm, Charles A. Gersbach, Rebecca D. Dodd, David G. Kirsch. Using CRISPR/Cas9 to generate primary soft tissue sarcoma in genetically engineered and wild-type mice [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 2810. doi:10.1158/1538-7445.AM2017-2810

Duke Scholars

Published In

Cancer Research

DOI

EISSN

1538-7445

ISSN

0008-5472

Publication Date

July 1, 2017

Volume

77

Issue

13_Supplement

Start / End Page

2810 / 2810

Publisher

American Association for Cancer Research (AACR)

Related Subject Headings

  • Oncology & Carcinogenesis
  • 3211 Oncology and carcinogenesis
  • 3101 Biochemistry and cell biology
  • 1112 Oncology and Carcinogenesis
 

Citation

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Huang, J., Chen, M., Whitley, M. J., Kuo, H.-C., Walens, A., Mowery, Y. M., … Kirsch, D. G. (2017). Abstract 2810: Using CRISPR/Cas9 to generate primary soft tissue sarcoma in genetically engineered and wild-type mice. In Cancer Research (Vol. 77, pp. 2810–2810). American Association for Cancer Research (AACR). https://doi.org/10.1158/1538-7445.am2017-2810
Huang, Jianguo, Mark Chen, Melodi J. Whitley, Hsuan-Cheng Kuo, Andrea Walens, Yvonne M. Mowery, David V. Mater, et al. “Abstract 2810: Using CRISPR/Cas9 to generate primary soft tissue sarcoma in genetically engineered and wild-type mice.” In Cancer Research, 77:2810–2810. American Association for Cancer Research (AACR), 2017. https://doi.org/10.1158/1538-7445.am2017-2810.
Huang J, Chen M, Whitley MJ, Kuo H-C, Walens A, Mowery YM, et al. Abstract 2810: Using CRISPR/Cas9 to generate primary soft tissue sarcoma in genetically engineered and wild-type mice. In: Cancer Research. American Association for Cancer Research (AACR); 2017. p. 2810–2810.
Huang, Jianguo, et al. “Abstract 2810: Using CRISPR/Cas9 to generate primary soft tissue sarcoma in genetically engineered and wild-type mice.” Cancer Research, vol. 77, no. 13_Supplement, American Association for Cancer Research (AACR), 2017, pp. 2810–2810. Crossref, doi:10.1158/1538-7445.am2017-2810.
Huang J, Chen M, Whitley MJ, Kuo H-C, Walens A, Mowery YM, Mater DV, Eward W, Cardona DM, Luo L, Ma Y, Nelson CE, Robinson-Hamm JN, Gersbach CA, Dodd RD, Kirsch DG. Abstract 2810: Using CRISPR/Cas9 to generate primary soft tissue sarcoma in genetically engineered and wild-type mice. Cancer Research. American Association for Cancer Research (AACR); 2017. p. 2810–2810.

Published In

Cancer Research

DOI

EISSN

1538-7445

ISSN

0008-5472

Publication Date

July 1, 2017

Volume

77

Issue

13_Supplement

Start / End Page

2810 / 2810

Publisher

American Association for Cancer Research (AACR)

Related Subject Headings

  • Oncology & Carcinogenesis
  • 3211 Oncology and carcinogenesis
  • 3101 Biochemistry and cell biology
  • 1112 Oncology and Carcinogenesis