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Development of transplantable human chordoma xenograft for preclinical assessment of novel therapeutic strategies.


ABSTRACT:

Background

Chordomas are rare and indolent bone tumors that arise in the skull base and mobile spine. Distant metastases occur in >20% of cases, but morbidity and mortality are mainly related to local relapses that affect the majority of patients. Standard chemotherapy has modest activity, whereas new targeted therapies (alone or in combination) have some activity in controlling disease progression. However, the scarcity of preclinical models capable of testing in vivo responses to these therapies hampers the development of new medical strategies.

Methods

In this study, 8 chordoma samples taken from 8 patients were implanted in nude mice. Four engrafted successfully and gave rise to tumor masses that were analyzed histologically, by means of fluorescence in situ hybridization and biochemical techniques. The data relating to each of the mouse tumors were compared with those obtained from the corresponding human tumor.

Results

All 4 engraftments retained the histological, genetic and biochemical features of the human tumors they came from. In one epidermal growth factor receptor(EGFR)-positive xenograft, responsiveness to lapatinib was evaluated by comparing the pre- and post treatment findings. The treatment induced a low-level, heterogeneous switching off of EGFR and its downstream signaling effectors.

Conclusions

Overall, this model is very close to human chordoma and represents a new means of undertaking preclinical investigations and developing tailored therapies.

SUBMITTER: Bozzi F 

PROVIDER: S-EPMC3870831 | biostudies-literature | 2014 Jan

REPOSITORIES: biostudies-literature

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Publications

Development of transplantable human chordoma xenograft for preclinical assessment of novel therapeutic strategies.

Bozzi Fabio F   Manenti Giacomo G   Conca Elena E   Stacchiotti Silvia S   Messina Antonella A   Dagrada GianPaolo G   Gronchi Alessandro A   Panizza Pietro P   Pierotti Marco A MA   Tamborini Elena E   Pilotti Silvana S  

Neuro-oncology 20140101 1


<h4>Background</h4>Chordomas are rare and indolent bone tumors that arise in the skull base and mobile spine. Distant metastases occur in >20% of cases, but morbidity and mortality are mainly related to local relapses that affect the majority of patients. Standard chemotherapy has modest activity, whereas new targeted therapies (alone or in combination) have some activity in controlling disease progression. However, the scarcity of preclinical models capable of testing in vivo responses to these  ...[more]

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