Rhabdomyosarcomas in aging A/J mice
Ontology highlight
ABSTRACT: Rhabdomyosarcomas (RSCs) are skeletal muscle neoplasms found in humans and domestic mammals. The A/J inbred strain developed a high frequency of RSC by 20 months of age while BALB/cJ and BALB/cByJ also develop RSC but less frequently. These neoplasms affected skeletal muscle surrounding either the axial or proximal appendicular skeleton and were characterized by pleomorphic cells with abundant eosinophilic cytoplasm, multiple nuclei, and cross striations that invaded locally. The diagnosis was confirmed by detection of alpha-sarcomeric actin and myogenin in the neoplastic cells using immunocytochemistry. The A/J strain, but not the related BALB/c substrains, is also characterised by a progressive muscular dystrophy homologous to limb-girdle muscular dystrophy type 2B. The association betwe
ORGANISM(S): Mus musculus
SUBMITTER: Roger Sher
PROVIDER: E-GEOD-29775 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
ACCESS DATA