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PMID: 9398859 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

EWS/FLI1-induced manic fringe renders NIH 3T3 cells tumorigenic.

Nature genetics ·Vol. 17 ·No. 4 ·1997-12-00 ·Pages 495-7

May WA, Arvand A, Thompson AD, Braun BS, Wright M, Denny CT

Abstract

EWS/FLI1, a fusion gene found in Ewing's sarcoma, encodes a transcriptional regulator and promotes cellular transformation by modulating the transcription of specific target genes. We have found that EWS/FLI1 and structurally related fusion proteins upregulate manic fringe (MFNG), a recently described member of the Fringe gene family instrumental in somatic development. MFNG is also expressed in human tumour-derived cell lines expressing EWS/FLI1. Overexpression of MFNG in NIH 3T3 cells renders them tumorigenic in mice with severe combined immunodeficiency disease (SCID). These data demonstrate that part of the oncogenic effect of EWS/FLI1 is to transcriptionally deregulate a member of a family of morphogenic genes.

MeSH Terms
3T3 Cells Animals Cell Transformation, Neoplastic/genetics Gene Expression Regulation, Neoplastic Glucosyltransferases Mice Mice, SCID Neoplasm Transplantation Oncogene Proteins, Fusion/genetics,physiology Protein Biosynthesis Proteins/genetics Proto-Oncogene Protein c-fli-1 RNA-Binding Protein EWS Sarcoma, Ewing/etiology,genetics Transcription Factors/genetics,physiology Tumor Cells, Cultured
Chemicals
EWS-FLI fusion protein Oncogene Proteins, Fusion Proteins Proto-Oncogene Protein c-fli-1 RNA-Binding Protein EWS Transcription Factors Glucosyltransferases Mfng protein, mouse
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
May W A
Department of Pediatrics, University of Alabama at Birmingham School of Medicine, USA.
Arvand A
Thompson A D
Braun B S
Wright M
Denny C T
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
1997-12-00
Pages
495-7
Language
English
Region
United States
NLM ID
9216904
Subset
IM
Grants
NCI NIH HHS · CA13148 · United States
NCI NIH HHS · CA32737 · United States
NIGMS NIH HHS · GM08042 · United States
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