A new mouse model for the study of neurofibromatosis

Research specialist Lia Thornberry Kent works under a fume hood dispersing a feeder solution necessary to maintain growing stem cell cultures in researcher James Thomson's lab at the University of Wisconsin-Madison. Thomson, a developmental biologist and professor of anatomy, directed the research group that reported the first isolation of embryonic stem cell lines from a nonhuman primate in 1995, work that led his group to the first successful isolation of human embryonic stem cell lines in 1998.
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The research group of the neurofibromatosis of the Catalan Institute of Oncology (ICO), the Institute of Biomedical Research of Bellvitge (IDIBELL) and the Institute of Medicicina Predictive and Personalized Cancer (IMPPC) has developed new mouse models for the study of principal malignant tumor associated with neurofibromatosis type 1.

Details of the development and characterization of new animal models have been published in EMBO Molecular Medicine.

Neurofibromatosis, a rare disease

The neurofibromatosis are disorders of the nervous system that primarily affect the development and growth of neural tissue cells.

Neurofibromatosis type 1 is the most common form, affecting one in 3,500 people, approximately. It is caused by mutations in the NF1 gene, located on chromosome 17. The involvement of this gene can cause a diverse range of health problems, such as tumors on the skin and nervous system.

In this sense, the primary malignant tumor associated with neurofibromatosis type 1 is called malignant tumor of the peripheral nerve sheath. It belongs to the group of soft tissue sarcomas, there is no effective treatment and is associated with poor survival.

New animal models

ICO-IDIBELL-IMPPC team has created what is called orthotopic tumor models, ie have successfully implanted human tumor mouse relevant body and develop as you would in person. The EMBO Molecular Medicine study shows how the animal model reproduces histological, genetic and epigenetic human tumor characteristics and patterns of spread, which is not achieved with other methods of implementation.

Until now there were no animal models based on direct transplantation of primary tumors originating in these patients. This group has generated five different models using immunosuppressed mice implanted with malignant tumors of peripheral nerve sheath in the same tissue where the tumors originate in humans. These animal models allow a better study of tumor and promote personalized medicine. If required, you might have a mouse with tumor of each patient so that you can predict how it will develop and decide in each case what the most appropriate treatment for each patient will be.

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