Browsing Chester Medical School by Subjects
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The hormone response element mimic sequence of GAS5 lncRNA is sufficient to induce apoptosis in breast cancer cells.(Impact Journals, 2016-02-03)Growth arrest-specific 5 (GAS5) lncRNA promotes apoptosis, and its expression is down-regulated in breast cancer. GAS5 lncRNA is a decoy of glucocorticoid/related receptors; a stem-loop sequence constitutes the GAS5 hormone response element mimic (HREM), which is essential for the regulation of breast cancer cell apoptosis. This preclinical study aimed to determine if the GAS5 HREM sequence alone promotes the apoptosis of breast cancer cells. Nucleofection of hormone-sensitive and -insensitive breast cancer cell lines with a GAS5 HREM DNA oligonucleotide increased both basal and ultraviolet-C-induced apoptosis, and decreased culture viability and clonogenic growth, similar to GAS5 lncRNA. The HREM oligonucleotide demonstrated similar sequence specificity to the native HREM for its functional activity and had no effect on endogenous GAS5 lncRNA levels. Certain chemically modified HREM oligonucleotides, notably DNA and RNA phosphorothioates, retained pro-apoptotic. activity. Crucially the HREM oligonucleotide could overcome apoptosis resistance secondary to deficient endogenous GAS5 lncRNA levels. Thus, the GAS5 lncRNA HREM sequence alone is sufficient to induce apoptosis in breast cancer cells, including triple-negative breast cancer cells. These findings further suggest that emerging knowledge of structure/function relationships in the field of lncRNA biology can be exploited for the development of entirely novel, oligonucleotide mimic-based, cancer therapies.
The long non-coding RNA NEAT1 regulates cell survival in breast cancer cell lines(NCRI Cancer Conference 2015 Abstracts, 2015)Background Nuclear long non-coding RNAs (LncRNAs) regulate various cellular processes including the organization of nuclear sub-structures, the alteration of chromatin state, and the regulation of gene expression. Nuclear Enriched Abundant Transcript 1 (NEAT1) is a nuclear lncRNA transcribed from chromosome 11q13. Two transcripts are produced from the NEAT1 gene, 3.7-kb NEAT1_v1 and 23-kb NEAT1_v2. Both isoforms participate in the formation of the nuclear paraspeckles . NEAT1 is reported to be overexpressed in prostate cancer and a direct transcriptional target of hypoxia-inducible factor in many breast cancer cell lines. The aims of this study were to determine the effects of silencing NEAT1 on breast cancer cell survival. Method MCF7 and MDA-MB 231 cells were transfected with siRNAs to different NEAT1 sequences or NEAT1 antisense oligonucleotides (ASO). Controls received scrambled siRNA or scrambled oligonucleotide, as appropriate. In some experiments, cells were exposed to ultraviolet-C (UV-C) light post-transfection to induce apoptosis, and then culture viability and apoptosis were assessed. NEAT1 expression was evaluated by qRT-PCR TaqMan® analysis. Results In MCF7 and MDA-MB-231 cells, siRNA-mediated silencing of NEAT1 reduced basal survival and after UV-C irradiation and decreased their colony forming ability. NEAT1 ASOs were more effective in silencing NEAT1 and caused a greater reduction in cell viability. NEAT1 silencing also affected cell cycle profile by enhancing the proportion of cells in G0/G1 phase. Conclusion NEAT1 regulates the survival of Breast cells. Down regulation of NEAT1 expression decreased cell survival, proliferation and modulated cell cycle progression of breast cancer cells, indicating a link between the NEAT1 expression levels and carcinogenesis of breast cancer.