Targeting oxidative stress in embryonal rhabdomyosarcoma.
Targeting oxidative stress in embryonal rhabdomyosarcoma.
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DOI:
10.1016/j.ccr.2013.11.002
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发表时间:
2013-12-09
期刊:
影响因子:
50.3
通讯作者:
St. Jude Children’s Research Hospital–Washington University Pediatric Cancer Genome Project
中科院分区:
文献类型:
--
作者:
Chen X;Stewart E;Shelat AA;Qu C;Bahrami A;Hatley M;Wu G;Bradley C;McEvoy J;Pappo A;Spunt S;Valentine MB;Valentine V;Krafcik F;Lang WH;Wierdl M;Tsurkan L;Tolleman V;Federico SM;Morton C;Lu C;Ding L;Easton J;Rusch M;Nagahawatte P;Wang J;Parker M;Wei L;Hedlund E;Finkelstein D;Edmonson M;Shurtleff S;Boggs K;Mulder H;Yergeau D;Skapek S;Hawkins DS;Ramirez N;Potter PM;Sandoval JA;Davidoff AM;Mardis ER;Wilson RK;Zhang J;Downing JR;Dyer MA;St. Jude Children’s Research Hospital–Washington University Pediatric Cancer Genome Project
Rhabdomyosarcoma is a soft-tissue sarcoma with molecular and cellular features of developing skeletal muscle. Rhabdomyosarcoma has two major histological subtypes, embryonal and alveolar, each with distinct clinical, molecular, and genetic features. Genomic analysis show 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 rhabdomyosarcoma (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.
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影响因子:
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通讯作者:
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DOI:
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发表时间:
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影响因子:
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