Sirt1 antisense transcript is down-regulated in human tumors
Neda Mokhberian1, Seyed Mahmoud Hashemi2,3, Vahid Jajarmi4
1Department of Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abstract:
Natural antisense transcripts (NATs) have recently been associated with the development of human cancers. Recent studies have shown that a natural antisense transcript (NAT) is present in Sirt1 gene which encodes a NAD-dependent deacetylase. Interestingly, expression of Sirt1 mRNA changes during development and progression of human cancers. However, it remains unclear to what extent Sirt1 antisense transcript (AS) may contribute to changes in the expression of Sirt1 mRNA. To determine this, we used quantitative measurement of RNA to reveal relationship between Sirt1 mRNA and Sirt1-AS across human cancer tissues, cell lines and stem cells. While Sirt1 mRNA level was increased in cancer cell lines and cancer tissues, the expression level of Sirt1-AS was lower in cancers compared to controls. This inverse correlation was observed in the expression of Sirt1 sense and antisense transcripts in normal and cancer tissues suggesting a functional role for Sirt1-AS in regulation of Sirt1 mRNA.
Insights
Natural antisense transcripts (NATs) regulate Sirt1 gene expression in cancer. Sirt1 mRNA increases while its antisense transcript (AS) decreases in tumors, suggesting a functional role for Sirt1-AS in cancer development.
Area of Science:
- Molecular Biology
- Cancer Research
- Gene Regulation
Background:
- Natural antisense transcripts (NATs) are implicated in human cancer development.
- The Sirt1 gene, encoding a NAD-dependent deacetylase, shows altered mRNA expression during cancer progression.
Purpose of the Study:
- To investigate the relationship between Sirt1 mRNA and its antisense transcript (Sirt1-AS) in various cancer models.
- To determine the potential regulatory role of Sirt1-AS in Sirt1 mRNA expression.
Main Methods:
- Quantitative RNA measurement was employed.
- Expression levels of Sirt1 mRNA and Sirt1-AS were analyzed across human cancer tissues, cell lines, and stem cells.
Main Results:
- Sirt1 mRNA levels were elevated in cancer cell lines and tissues compared to controls.
- Conversely, Sirt1-AS expression was reduced in cancers.
- An inverse correlation was observed between Sirt1 sense and antisense transcript levels in normal and cancerous tissues.
Conclusions:
- Sirt1-AS exhibits an inverse correlation with Sirt1 mRNA in human cancers.
- These findings suggest a functional role for Sirt1-AS in regulating Sirt1 mRNA expression within the context of cancer.
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