PATIENT-DERIVED XENOGRAFTS AS A PRECLINICAL MODEL FOR BONE SARCOMAS

ABSTRACT Objective: The purpose of this study was to reproduce a mouse model of bone sarcomas for use in cancer research. Methods: A fresh sample of the tumor tissue was implanted subcutaneously into nude mice. When the patient-derived xenograft (PDX) reached a volume of 1500 mm3, it was harvested...

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Main Authors: WALTER MEOHAS, REGINA ALCANTARA GRANATO, JOÃO ANTONIO MATHEUS GUIMARÃES, RHAYRA BRAGA DIAS, ANNELIESE FORTUNA-COSTA, MARIA EUGENIA LEITE DUARTE
Format: Article
Language:English
Published: Sociedade Brasileira de Ortopedia e Traumatologia 2018-04-01
Series:Acta Ortopédica Brasileira
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Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-78522018000200098&tlng=en
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author WALTER MEOHAS
REGINA ALCANTARA GRANATO
JOÃO ANTONIO MATHEUS GUIMARÃES
RHAYRA BRAGA DIAS
ANNELIESE FORTUNA-COSTA
MARIA EUGENIA LEITE DUARTE
author_facet WALTER MEOHAS
REGINA ALCANTARA GRANATO
JOÃO ANTONIO MATHEUS GUIMARÃES
RHAYRA BRAGA DIAS
ANNELIESE FORTUNA-COSTA
MARIA EUGENIA LEITE DUARTE
author_sort WALTER MEOHAS
collection DOAJ
description ABSTRACT Objective: The purpose of this study was to reproduce a mouse model of bone sarcomas for use in cancer research. Methods: A fresh sample of the tumor tissue was implanted subcutaneously into nude mice. When the patient-derived xenograft (PDX) reached a volume of 1500 mm3, it was harvested for re-implantation into additional mice. Histology was used to compare the morphological characteristics of different generations of sarcoma xenografts with the primary tumor. Results: Sixteen sarcoma tissue samples were engrafted into nude mice. Nine patients were diagnosed with osteosarcoma, two with chondrosarcoma, two with malignant peripheral nerve sheath tumor, one with synovial sarcoma, one with pleomorphic sarcoma, and one with Ewing’s sarcoma. PDX tumors were generated in 11 of the 16 implanted specimens (69% success rate in P1). Six P1 tumors grew sufficiently for transfer into additional mice, producing the P2 generation, and three P2 tumors established the P3 generation. Conclusion: PDX tumors generated from bone sarcomas were successfully established in immunodeficient mice and reproduced the characteristics of the primary tumor with a high degree of fidelity. The preclinical PDX model described herein may represent an important tool for translational oncology research and for evaluating therapeutic strategies for bone sarcomas. Level of Evidence I; Experimental study.
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spelling doaj.art-4bde8b12155148258ebf8cf673c10ce92022-12-22T04:16:23ZengSociedade Brasileira de Ortopedia e TraumatologiaActa Ortopédica Brasileira1413-78522018-04-012629810210.1590/1413-785220182602186998PATIENT-DERIVED XENOGRAFTS AS A PRECLINICAL MODEL FOR BONE SARCOMASWALTER MEOHAShttps://orcid.org/0000-0003-1402-9667REGINA ALCANTARA GRANATOhttps://orcid.org/0000-0001-9060-9052JOÃO ANTONIO MATHEUS GUIMARÃEShttps://orcid.org/0000-0002-5647-2248RHAYRA BRAGA DIAShttps://orcid.org/0000-0001-5465-1149ANNELIESE FORTUNA-COSTAhttps://orcid.org/0000-0002-3507-0493MARIA EUGENIA LEITE DUARTEhttps://orcid.org/0000-0003-2248-2410ABSTRACT Objective: The purpose of this study was to reproduce a mouse model of bone sarcomas for use in cancer research. Methods: A fresh sample of the tumor tissue was implanted subcutaneously into nude mice. When the patient-derived xenograft (PDX) reached a volume of 1500 mm3, it was harvested for re-implantation into additional mice. Histology was used to compare the morphological characteristics of different generations of sarcoma xenografts with the primary tumor. Results: Sixteen sarcoma tissue samples were engrafted into nude mice. Nine patients were diagnosed with osteosarcoma, two with chondrosarcoma, two with malignant peripheral nerve sheath tumor, one with synovial sarcoma, one with pleomorphic sarcoma, and one with Ewing’s sarcoma. PDX tumors were generated in 11 of the 16 implanted specimens (69% success rate in P1). Six P1 tumors grew sufficiently for transfer into additional mice, producing the P2 generation, and three P2 tumors established the P3 generation. Conclusion: PDX tumors generated from bone sarcomas were successfully established in immunodeficient mice and reproduced the characteristics of the primary tumor with a high degree of fidelity. The preclinical PDX model described herein may represent an important tool for translational oncology research and for evaluating therapeutic strategies for bone sarcomas. Level of Evidence I; Experimental study.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-78522018000200098&tlng=enBone neoplasms. Sarcomaexperimental. Translational medical research
spellingShingle WALTER MEOHAS
REGINA ALCANTARA GRANATO
JOÃO ANTONIO MATHEUS GUIMARÃES
RHAYRA BRAGA DIAS
ANNELIESE FORTUNA-COSTA
MARIA EUGENIA LEITE DUARTE
PATIENT-DERIVED XENOGRAFTS AS A PRECLINICAL MODEL FOR BONE SARCOMAS
Acta Ortopédica Brasileira
Bone neoplasms. Sarcoma
experimental. Translational medical research
title PATIENT-DERIVED XENOGRAFTS AS A PRECLINICAL MODEL FOR BONE SARCOMAS
title_full PATIENT-DERIVED XENOGRAFTS AS A PRECLINICAL MODEL FOR BONE SARCOMAS
title_fullStr PATIENT-DERIVED XENOGRAFTS AS A PRECLINICAL MODEL FOR BONE SARCOMAS
title_full_unstemmed PATIENT-DERIVED XENOGRAFTS AS A PRECLINICAL MODEL FOR BONE SARCOMAS
title_short PATIENT-DERIVED XENOGRAFTS AS A PRECLINICAL MODEL FOR BONE SARCOMAS
title_sort patient derived xenografts as a preclinical model for bone sarcomas
topic Bone neoplasms. Sarcoma
experimental. Translational medical research
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-78522018000200098&tlng=en
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