期刊文献+

肺癌与慢性阻塞性肺病的表观遗传学 被引量:1

Lung cancer and its epigenetics association with chronic obstructive pulmonary disease
原文传递
导出
摘要 肺癌是严重影响人类健康的恶性肿瘤之一,影响肺癌发病的表观遗传学机制已成为近年来的研究热点。慢性阻塞性肺病(chronicobstructivepulmonarydisease,COPD)不但是肺癌的常见合并症,而且可能是肺癌的独立风险因素。肺癌和COPD在表观遗传学水平的改变主要涉及DNA甲基化、组蛋白修饰和非编码RNA调控等。探讨肺癌与COPD在表观遗传学水平的改变及其相互关系,可为肺癌及COPD的发病机制、疾病进展、疾病预后等提供更为广阔的视角,并为疾病的治疗开辟新的方向。 Lung cancer and chronic obstructive pulmonary disease (COPD) are the leading causes of morbidity and mortality worldwide. Development of lung cancer involves both genetic and environment factors. In addition to genetic alterations, epigenetic mechanism is closely involved in pathogenesis of lung cancer. Characterized by an abnormal persistent inflammatory response to noxious environmental stimulation, COPD has shown to increase the susceptibility for lung tumorigenesis in previous research. Current research on epigenetics of lung cancer and COPD has focused on aberrant DNA methylation, histone acetylation and non-coding RNAs regulation. The aberrant DNA methylation associated with lung cancer and COPD has included overexpression of DNA methyltransferase, global DNA hypomethylation and DNA hypermethylation in promoter regions, while histone acetylation and histone methylation are the major changes for histone modification, in which histone acetyltransferases, histone deacetylases, histone methyltransferases and histone demethylases play the most important roles. RNA interference and microRNAs are both hot topics of research on non-coding RNAs regulation. Understanding of concurrent epigenetic alterations in the pathogenesis of lung cancer and COPD may facilitate identification of specific therapeutic targets and development of effective treatment.
出处 《中华医学遗传学杂志》 CAS CSCD 北大核心 2013年第1期70-73,共4页 Chinese Journal of Medical Genetics
基金 国家自然科学基金项目(81072257)
关键词 肺癌 慢性阻塞性肺病 表观遗传学 DNA甲基化 组蛋白修饰 非编码RNA Lung cancer Chronic obstructive pulmonary disease Epigenetics DNA methylation Histone modification Non-coding RNA
  • 相关文献

参考文献1

二级参考文献14

  • 1李昂,闫文生,梁启万,刘继红,王家祥,赵松,方嬿.应用寡核苷酸芯片鉴别肺鳞癌Ⅰb期特异相关基因[J].中华医学杂志,2005,85(37):2623-2628. 被引量:2
  • 2Kalinichenko VV, Major ML, Wang X, et al. Foxmlb transcription factor is essential for development of hepatocellular carcinomas and is negatively regulated by the pl9ARF tumor suppressor. Genes Dev, 2004, 18: 830-850. 被引量:1
  • 3Madureira PA, Varshochi R, Constantinidou D, et al. The Forkhead box M1 protein regulates the transcription of the estrogen receptor alpha in breast cancer cells. J Biol Chem, 2006, 281: 25167-25176. 被引量:1
  • 4Liu M, Dai B, Kang SH, et al. FoxM1B is overexpressed in human glioblastomas and critically regulates the tumorigenicity of glioma cells. Cancer Res, 2006, 66 : 3593-3602. 被引量:1
  • 5Wang Z, Banerjee S, Kong D, et al. Down-regulation of Forkhead Box M1 transcription factor leads to the inhibition of invasion and angiogenesis of pancreatic cancer cells. Cancer Res, 2007, 67: 8293-8300. 被引量:1
  • 6Kim IM, Ackerson T, Ramakrishna S, et al. The Forkhead Box M1 transcription factor stimulates the proliferation of tumor cells during development of lung cancer. Cancer Res, 2006, 66 : 2153-2161. 被引量:1
  • 7Radhakrishnan SK, Bhat UG, Hughes DE, et al. Identification of a chemical inhibitor of the oncogenic transcription factor Forkhead Box M1. Cancer Res, 2006, 66: 9731-9735. 被引量:1
  • 8Gusarova GA, Wang IC, Major ML, et al. A cell-penetrating ARF peptide inhibitor of FoxM1 in mouse hepatocellular carcinoma treatment. Clin Invest, 2007, 117: 99-111. 被引量:1
  • 9Wang IC, Chen YJ, Hughes D, et al. FoxM1 regulates transcription of JNK1 to promote the G1/S transition and tumor cell invasiveness. J Biol Chem, 2008, 283 : 20770-20778. 被引量:1
  • 10Dai B, Kang SH, Gong W, et al. Aberrant FoxM1B expression increases matrix metalloproteinase-2 transcription and enhances the invasion of glioma cells. Oncogene, 2007, 26 : 6212-6219. 被引量:1

共引文献9

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部