Targeting Oxidative Stress in Embryonal Rhabdomyosarcoma

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• 作者：Xiang Chen ; Elizabeth Stewart ; Anang聽A. Shelat ; Chunxu Qu ; Armita Bahrami ; Mark Hatley ; Gang Wu ; Cori Bradley ; Justina McEvoy ; Alberto Pappo ; Sheri Spunt ; Marcus聽B. Valentine ; Virginia Valentine ; Fred Krafcik ; Walter聽H. Lang ; Monika Wierdl ; Lyudmila Tsurkan ; Viktor Tolleman ; Sara聽M. Federico ; Chris Morton ; et al.
• 刊名：Cancer Cell
• 出版年：9 December, 2013
• 年：2013
• 卷：24
• 期：6
• 页码：710-724
• 全文大小：5413 K

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Summary

Rhabdomyosarcoma is a soft-tissue sarcoma with molecular and cellular features of developing skeletal muscle. Rhabdomyosarcoma has two major histologic subtypes, embryonal and alveolar, each with distinct clinical, molecular, and genetic features. Genomic analysis shows that embryonal tumors have more structural and copy number variations than alveolar tumors. Mutations in the RAS/NF1 pathway are significantly associated with intermediate- and high-risk embryonal rhabdomyosarcomas (ERMS). In contrast, alveolar rhabdomyosarcomas (ARMS) have fewer genetic lesions overall and no known recurrently mutated cancer consensus genes. To identify therapeutics for ERMS, we developed and characterized orthotopic xenografts of tumors that were sequenced in our study. High-throughput screening of primary cultures derived from those xenografts identified oxidative stress as a pathway of therapeutic relevance for ERMS.