Circadian Expression of Clock- and Tumor Suppressor Genes in Human Oral Mucosa

昼夜节律 时钟 生物 生物钟 微阵列 基因 微阵列分析技术 基因表达 永恒的 句号(音乐) 基因表达谱 遗传学 内分泌学 物理 声学
作者
Derek Zieker,Isabel Jenne,Ingmar Koenigsrainer,Marty Zdichavsky,Kay Nieselt,Katharina Buck,Judith Zieker,Stefan Beckert,Joerg Glatzle,Rainer Spanagel,Alfred Koenigsrainer,Hinnak Northoff,Markus Loeffler
出处
期刊:Cellular Physiology and Biochemistry [Karger Publishers]
卷期号:26 (2): 155-166 被引量:39
标识
DOI:10.1159/000320547
摘要

Circadian rhythms are daily oscillations of multiple biological processes driven by endogenous clocks. Imbalance of these rhythms has been associated with cancerogenesis in humans. To further elucidate the role circadian clocks have in cellular growth control, tumor suppression and cancer treatment, it is revealing to know how clock genes and clock-controlled genes are regulated in healthy humans.Therefore comparative microarray analyses were conducted investigating the relative mRNA expression of clock genes throughout a 24-hour period in cell samples obtained from oral mucosa of eight healthy diurnally active male study participants. Differentially expressed selected genes of interest were additionally evaluated using qRT-PCR.Microarray analysis revealed 33 significant differentially regulated clock genes and clock- controlled genes, throughout a one day period (6.00h, 12.00h, 18.00h, 24.00h). Hereof were 16 clock genes and 17 clock- controlled genes including tumor suppressor- and oncogenes. qRT-PCR of selected genes of interest, such as hPER2, hCRY1, hBMAL1, hCCRN4L and hSMAD5 revealed significant circadian regulations.Our study revealed a proper circadian regulation profile of several clock- and tumor suppressor genes at defined points in time in the participants studied. These findings could provide important information regarding genes displaying the same expression profile in the gastrointestinal tract amounting to a physiological expression profile of healthy humans. In the future asynchronous regulations of those genes might be an additional assistant method to detect derivations distinguishing normal from malignant tissue or assessing risk factors for cancer.
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