4.7 Article

Establishment and Characterization of Feline Mammary Tumor Patient-Derived Xenograft Model

Journal

ANIMALS
Volume 11, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/ani11082380

Keywords

feline mammary tumor; patient-derived xenograft; cell line

Funding

  1. Ministry of Science and Technology (Taiwan) [MOST106-2313-B-005-059-and MOST107-2311-B-005-011-MY3]

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The study successfully established a PDX model for feline mammary tumors, preserving important features of the original tumor, including distant metastasis. This provides a platform for translational research on FMT.
Simple Summary Feline mammary tumor (FMT) is a relatively commonly diagnosed neoplasm in the cat. Development of new veterinary cancer therapies is limited by the shortage of in vivo models that reproduce tumor microenvironment and metastatic progression. In this study, FMT patient-derived xenografts (PDX) model were established and primary cell line isolated from orthotopic PDX. The tumor grafts conserve original tumor essential features, including distant metastasis. FMT-PDX represents an available resource for bridging the biology of FMT with preclinical studies of FMT in cats. Feline mammary tumor is a relatively commonly diagnosed neoplasm in the cat. Development of new veterinary cancer therapies is limited by the shortage of in vivo models that reproduce tumor microenvironment and metastatic progression. Four feline mammary tumor orthotopic patient-derived xenograft model (PDX) successfully established in NOD-SCID gamma (NSG) mice. The overall success rate of PDX establishment was 36% (4/11). Histological, immunohistochemical, and short tandem repeat analysis showed a remarkable similarity between patient's tumor and xenograft. The tumor grafts conserve original tumor essential features, including distant metastasis. Primary FMT-1807 cell line isolated from FMT-1807PDX tumor tissue. Tumorigenicity of FMT-1807 cells expanded from PDX was assessed by orthotopic injection into NSG mice. Mice yielded tumors which preserve the lung and liver metastasis ability. This work provides a platform for FMT translational investigation.

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