NIH, 37 Convent Dr #3122, Bethesda, MD 20892-4255.
Mol Cancer Res. 2014 Jan;12(1):82-90. doi: 10.1158/1541-7786.MCR-13-0392. Epub 2013 Dec 2.
We report that HMGN1, a nucleosome-binding protein that affects chromatin structure and function, affects the growth of N-nitrosodiethylamine (DEN)-induced liver tumors. Following a single DEN injection at 2 weeks of age, Hmgn1(tm1/tm1) mice, lacking the nucleosome-binding domain of HMGN1, had earlier signs of liver tumorigenesis than their Hmgn1(+/+) littermates. Detailed gene expression profiling revealed significant differences between DEN-injected and control saline-injected mice, but only minor differences between the injected Hmgn1(tm1/tm1) mice and their Hmgn1(+/+) littermates. Pathway analysis revealed that the most significant process affected by loss of HMGN1 involves the lipid/sterol metabolic pathway. Our study indicates that in mice, loss of HMGN1 leads to transcription changes that accelerate the progression of DEN-induced hepatocarcinogenesis, without affecting the type of tumors or the final total tumor burden of these mice.
Loss of HMGN1 leads to accelerated progression of DEN-induced hepatocarcinogenesis in mice.
我们报告称,HMGN1 是一种核小体结合蛋白,可影响染色质结构和功能,它会影响 N-亚硝基二乙胺(DEN)诱导的肝肿瘤的生长。在 2 周龄时单次 DEN 注射后,缺乏 HMGN1 核小体结合域的 Hmgn1(tm1/tm1) 小鼠比其 Hmgn1(+/+) 同窝仔鼠更早出现肝肿瘤发生的迹象。详细的基因表达谱分析显示 DEN 注射和对照盐水注射的小鼠之间存在显著差异,但 DEN 注射的 Hmgn1(tm1/tm1) 小鼠与其 Hmgn1(+/+) 同窝仔鼠之间仅有较小差异。途径分析表明,受 HMGN1 缺失影响最显著的过程涉及脂质/固醇代谢途径。我们的研究表明,在小鼠中,HMGN1 的缺失会导致转录变化,从而加速 DEN 诱导的肝癌发生的进展,而不影响这些小鼠的肿瘤类型或最终总肿瘤负担。
在小鼠中,HMGN1 的缺失会导致 DEN 诱导的肝癌发生加速进展。