ALL HISTOLOGICAL TYPES OF PRIMARY HUMAN RHABDOMYOSARCOMA EXPRESS ALPHA-CARDIAC AND NOT ALPHA-SKELETAL ACTIN MESSENGER-RNA

Citation
W. Schurch et al., ALL HISTOLOGICAL TYPES OF PRIMARY HUMAN RHABDOMYOSARCOMA EXPRESS ALPHA-CARDIAC AND NOT ALPHA-SKELETAL ACTIN MESSENGER-RNA, The American journal of pathology, 144(4), 1994, pp. 836-846
Citations number
66
Categorie Soggetti
Pathology
ISSN journal
00029440
Volume
144
Issue
4
Year of publication
1994
Pages
836 - 846
Database
ISI
SICI code
0002-9440(1994)144:4<836:AHTOPH>2.0.ZU;2-B
Abstract
Eleven human primary rhabdomyosarcomas (RMSs), including all histologi cal variants, were analyzed morphologically, immunohistochemically for intermediate filament proteins and actin isoforms, and by means of No rthern blots with probes specific for total actin, alpha-skeletal (SK) , alpha-cardiac (CARD), and alpha-smooth muscle actin messenger (m)RNA s. All tumors disclosed ultrastructural evidence of skeletal muscle fe atures with terminal differentiation in three cases. The RMSs containe d immunohistochemically the intermediate filament proteins vimentin an d desmin and reacted positively with the alpha-sarcomeric actin antibo dy, which recognizes alpha-SK and alpha-CARD actin isoforms. All RMSs reacted with the total actin probe, recognizing at 2.1 kb cytoplasmic actin mRNAs and at 1.7 kb alpha-actin mRNAs. With the specific probes, all RMSs expressed alpha-CARD actin mRNA, four neoplasms expressed al so alpha-smooth muscle actin mRNA, whereas the probe for alpha-SK acti n mRNA never produced a signal except in one case, in which the tumor masses were intermingled with non-neoplastic preexistent striated musc le fibers. Because alpha-CARD and alpha-smooth muscle actins are trans iently expressed during normal skeletal muscle development, RMSs seem to follow normal skeletal myogenesis without completing the final step , consisting of alpha-SK actin mRNA expression. The use of Northern bl ots for alpha-CARD actin as an adjunct to conventional techniques may be helpful for the precise identification of primary RMSs compared to other soft tissue neoplasms.