The research study, published in the October issue of Cancer Cell, provides evidence that a genetically engineered mouse model faithfully recapitulates treatment-associated cancers that occur in humans and may be useful for investigating the mechanisms involved in the development of therapy-induced cancers and for testing preventive strategies.

Secondary malignant neoplasms (SMNs) are new cancers that patients develop as a result of having received chemotherapy or radiation to treat a different type of cancer that may have occurred years earlier. To make matters worse, many of these secondary cancers are notoriously resistant to treatment. The occurrence of SMNs is a serious concern for doctors and patients, as the use of intensive radiation and chemotherapy has been more successful in curing primary cancers and has dramatically increased survival rates in children and adults. Unfortunately, as a result of treatment success, the incidence of SMNs has also risen. "The lack of relevant animal models of SMNs has impeded efforts to understand how mutagenic cancer therapeutics induce tumors in vivo, and to test preventive strategies," explains study author Dr. Kevin Shannon, a pediatric oncologist at the University of California, San Francisco.

Dr. Shannon and colleagues used a strain of mice developed in the laboratory of Dr. Tyler Jacks that carry a mutation in a tumor suppressor gene called Nf1. They selected this strain based on clinical data suggesting that humans who inherit this mutation are predisposed to SMNs. Nf1 mutant mice that were exposed to radiation, or radiation combined with chemotherapy, developed secondary cancers that are common in humans including leukemia, sarcoma, and breast cancers. "These animals develop a similar spectrum of malignancies as human patients who are treated with radiation and alkylating agents, and provide a tractable system for performing mechanistic studies, for comparing the mutagenic potential of different regimens, and for testing preventive strategies," offers Dr. Shannon. The study authors also suggest that this mouse model may be useful for testing novel therapeutic strategies for tumors that are resistant to conventional cancer therapies.

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