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PMID: 2601695 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Expression of the MyoD1 muscle determination gene defines differentiation capability but not tumorigenicity of human rhabdomyosarcomas.

Molecular and cellular biology ·Vol. 9 ·No. 11 ·1989-11-00 ·Pages 4722-30

Hiti AL, Bogenmann E, Gonzales F, Jones PA

Abstract

Several human rhabdomyosarcoma cell lines, cultured primary tumor explants, and biopsies of tumor and normal skeletal muscle tissue expressed a 2.0-kilobase transcript that hybridized to the mouse muscle determination gene MyoD1. This transcript was found in tumor cell lines and primary explants that developed multinucleated myotubes but was absent in Wilms' tumors or cell lines and primary explants that developed multinucleated myotubes but was absent in Wilms' tumors or cell lines derived from other mesenchymal tumor cell types. Expression of the human homolog of MyoD1 therefore can define a tumor as a rhabdomyosarcoma. Transfection of the mouse MyoD1 gene into the human rhabdomyosarcoma cell line RD increased the ability of the tumor cells to differentiate into multinucleated myotubes and enhanced myosin heavy-chain gene expression but did not decrease tumorigenicity in nude mice.

MeSH Terms
Animals Blotting, Northern Blotting, Southern Carcinogenicity Tests Cell Differentiation Cell Line Cell Transformation, Neoplastic Gene Expression Genes Humans Mice Muscles/cytology Myosins/analysis,genetics Rhabdomyosarcoma/genetics,pathology Transcription, Genetic Transfection Tumor Cells, Cultured
Chemicals
Myosins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hiti A L
Kenneth Norris Jr. Comprehensive Cancer Center, University of Southern California School of Medicine, Los Angeles 90033.
Bogenmann E
Gonzales F
Jones P A
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1989-11-00
Pages
4722-30
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC363619
Subset
IM
Grants
NEI NIH HHS · EY04950 · United States
NCI NIH HHS · R35-CA49758 · United States
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