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GAS5, a non-protein-coding RNA, controls apoptosis and is downregulated in breast cancer

Mourtada-Maarabouni, M; Pickard, M R; Hedge, V L; Farzaneh, F; Williams, G T

Authors

M R Pickard

V L Hedge

F Farzaneh

G T Williams



Contributors

M. Mourtada-Maarabouni
Other

M.R. Pickard
Other

V.L. Hedge
Other

F. Farzaneh
Other

G.T. Williams
Other

Abstract

Effective control of both cell survival and cell proliferation is critical to the prevention of oncogenesis and to successful cancer therapy. Using functional expression cloning, we have identified GAS5 (growth arrest-specific transcript 5) as critical to the control of mammalian apoptosis and cell population growth. GAS5 transcripts are subject to complex post-transcriptional processing and some, but not all, GAS5 transcripts sensitize mammalian cells to apoptosis inducers. We have found that, in some cell lines, GAS5 expression induces growth arrest and apoptosis independently of other stimuli. GAS5 transcript levels were significantly reduced in breast cancer samples relative to adjacent unaffected normal breast epithelial tissues. The GAS5 gene has no significant protein-coding potential but expression encodes small nucleolar RNAs (snoRNAs) in its introns. Taken together with the recent demonstration of tumor suppressor characteristics in the related snoRNA U50, our observations suggest that such snoRNAs form a novel family of genes controlling oncogenesis and sensitivity to therapy in cancer.

Citation

Mourtada-Maarabouni, M., Pickard, M. R., Hedge, V. L., Farzaneh, F., & Williams, G. T. (2009). GAS5, a non-protein-coding RNA, controls apoptosis and is downregulated in breast cancer. Oncogene, 28, 195–208. https://doi.org/10.1038/onc.2008.373

Journal Article Type Article
Acceptance Date Aug 20, 2008
Online Publication Date Oct 6, 2008
Publication Date Jan 15, 2009
Deposit Date May 16, 2024
Journal Oncogene
Print ISSN 1476-5594
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 28
Pages 195–208
ISBN 09509232 14765594
DOI https://doi.org/10.1038/onc.2008.373
Public URL https://keele-repository.worktribe.com/output/543734