التفاصيل البيبلوغرافية
| العنوان: |
Hepatic leukemia factor promotes resistance to cell death: Implications for therapeutics and chronotherapy |
| المؤلفون: |
Waters, Katrina M.1, Sontag, Ryan L.2, Weber, Thomas J.2 Thomas.Weber@pnl.gov |
| المصدر: |
Toxicology & Applied Pharmacology. Apr2013, Vol. 268 Issue 2, p141-148. 8p. |
| مصطلحات موضوعية: |
*LIVER cancer, *CELL death, *CLINICAL chronobiology, *CIRCADIAN rhythms, *GENE expression, *MOLECULAR biology, *TRANSCRIPTION factors, *LACTATE dehydrogenase |
| مستخلص: |
Abstract: Physiological variation related to circadian rhythms and aberrant gene expression patterns are believed to modulate therapeutic efficacy, but the precise molecular determinants remain unclear. Here we examine the regulation of cell death by hepatic leukemia factor (HLF), which is an output regulator of circadian rhythms and is aberrantly expressed in human cancers, using an ectopic expression strategy in JB6 mouse epidermal cells and human keratinocytes. Ectopic HLF expression inhibited cell death in both JB6 cells and human keratinocytes, as induced by serum-starvation, tumor necrosis factor alpha and ionizing radiation. Microarray analysis indicates that HLF regulates a complex multi-gene transcriptional program encompassing upregulation of anti-apoptotic genes, downregulation of pro-apoptotic genes, and many additional changes that are consistent with an anti-death program. Collectively, our results demonstrate that ectopic expression of HLF, an established transcription factor that cycles with circadian rhythms, can recapitulate many features associated with circadian-dependent physiological variation. [Copyright &y& Elsevier] |
| قاعدة البيانات: |
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