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ENEA (Ente Nuove technologie Energia e Ambiente) CRE Casaccia, Division of Molecular Biology, Via Anguillarese, 303, 00060 Rome, Italy [G. R., A. N., S. P., A. R.], and the Department of Microbiology and Jefferson Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107 [T. S., M. N-S., B. C.]
Transfection of a neuroblastoma cell line with expression vectors containing two different segments of human c-myb complementary DNA in antisense orientation yielded far fewer transfectant clones than did the transfection with the identical segments in sense orientation. In cell clones expressing c-myb antisense RNA, levels of the c-myb protein were down-regulated and the proliferation rate was slower than that of cells transfected with sense constructs or the untransfected parental cell lien. Treatment of neuroblastoma and neuroepithelioma cell lines with a c-myb antisense oligodeoxynucleotide strongly inhibited cell growth. These data indicate a definite involvement of c-myb in the proliferation of neuroectodermal tumor cells extending the role of this protooncogene beyond the hematopoietic system. The availability of cell clones that transcribe c-myb antisense RNA provides a useful tool to study the involvement of other genes in the proliferation and differentiation of neuroblastoma cells.
1 This work was supported in part by NIH Grant CA46782, by American Cancer Society Grant CH-455A, and by a grant from the Associazione Italiana Ricerca sul Cancro (AIRC).
2 To whom requests for reprints should be addressed, at ENEA (Ente technologie Energia e Ambiente) CRE Casaccia, Division of Molecular Biology, Via Anguillarese, 303, 00060 Rome, Italy (GR), or Department of Microbiology, Thomas Jefferson University, 10th and Locust Streets, Philadelphia, PA 19107 (BC).
3 Scholar of the Leukemia Society of America.
Received 12/13/91. Accepted 5/27/92.
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