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组蛋白去甲基酶JMJD3在肿瘤发生发展中的作用 被引量:4

Roles of Histone Demethylase JMJD3 in Tumorigenesis
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摘要 肿瘤的发生发展常常伴随着表观遗传的改变。组蛋白甲基化受表观遗传的调控,参与了多种生物学过程。JMJD3是一种组蛋白去甲基化酶,主要负责去除组蛋白H3第27位赖氨酸的甲基化修饰,在个体发育、衰老、炎症反应等过程中起到重要作用。近年研究发现,JMJD3在结肠癌、脑胶质瘤、乳腺癌等多种肿瘤中表达异常,并不同程度地影响了肿瘤的生长、迁移、侵袭等过程。该文对JMJD3在肿瘤发生发展中的作用及其潜在机制进行综述,以期靶向JMJD3为相关肿瘤的诊断与治疗提供新思路。 The development of tumors is often accompanied by epigenetic changes. Histone methylation was regulated by epigenetic regulation and was participated in a variety of biological processes. JMJD3, a histone demethylase, which was responsible for the removal of the methylation of di-and tri-methyl-lysine 27 on histone H3, plays important roles in the development of physiological process, such as individual development, senescence and inflammation. Recently, abnormal expressions of JMJD3 have been found in colon cancer, glioma, breast cancer and other tumors, which affect the growth, migration and invasion of these tumors to varying degrees. The role of JMJD3 in tumorigenesis and its underlying mechanisms was summarized so as to provide new ideas for the diag- nosis and treatment of related tumors through targeting JMJD3.
作者 殷梦月 曹柯欣 王慧 周长林 樊竑冶 YIN Meng-yue;CAO Ke-xin;WANG Hui;ZHOU Chang-lin;FAN Hong-ye(School of Life Science and Technology, China Pharmaceutical University, Nanjing 210009, China)
出处 《药物生物技术》 CAS 2018年第2期160-165,共6页 Pharmaceutical Biotechnology
基金 国家自然科学青年基金(No.81501403) 江苏省自然科学青年基金(No.BK20150700) 江苏高校品牌专业建设工程资助项目(No.PPZY2015A057) 中国药科大学药学基地科研训练及科研能力提高项目(No.J1310032) 江苏省级大学生创新创业训练计划项目
关键词 组蛋白去甲基化 基因激活 组蛋白去甲基酶 JMJD3 肿瘤 Histone demethylation Gene activation Histone demethylase JMJD3 Tumor
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  • 1胡贺芳,时辉,车国卫,罗凤鸣.肺癌组织中含十字形结构域蛋白3表达的意义[J].中国呼吸与危重监护杂志,2011,10(2):168-170. 被引量:6
  • 2KAWAZU M,SASO K, TONG K I, et al. Histone demethylase JMJD2B functions as a co-factor of estrogen receptor in breast cancer proliferation and mammary gland development [J]. PLoS One, 2011,6(3) : e17830.
  • 3CHO H S, SUZUKI T, DOHMAE N, et al. Demethylation of RB regulator MYPT1 by histone demethylase LSD1 promotes cell cycle progression in cancer cells[J]. Cancer Res, 2011, 71(3):655-660.
  • 4AGGER K, CLOOS P A, CHRISTENSEN J, et al. UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development [J]. Nature, 2007, 449 (7163) : 731-734.
  • 5BURGOLD T, SPREAFICO F, SANTA D F, et al. The histone H3 lysine 27-specific demethylase Jmjd3 is required for neural commitment[J]. PLoS One, 2008,3(8) : e3034.
  • 6MILLER S A, MOHN S E, WEINMANN A S. JMJD3 and UTX play a demethylaseqndependent role in ehromatin remodeling to regulate T-box family member-dependent gene expression[J]. Mol Cell, 2010, 40(4): 594-605.
  • 7URASHIMA M, TEOH G, CHAUHAN D, et al. Interleukin-6 overcomes p21WAF1 upregulation and G1 growth arrest induced by dexamethasone and interferon-gamma in multiple myeloma cells[J]. Blood, 1997, 90(1): 279-289.
  • 8HUBNER M R, SPECTOR D L. Role of H3K27 demethylasts JMJD3 and UTX in transcriptional regulation[J]. Cold Spring Harb Symp Quant Biol, 2011,75 : 43-49.
  • 9GARTEL A L, RADHAKRISHNAN S K. Lost in transcription : p21 repression, mechanisms, and consequences[J]. Cancer Res, 2005, 65(10): 3980-3985.
  • 10NIKOLOVA D A, ASANGANI I A, NELSON L D, et al. Cetuximab attenuates metastasis and u-par expression in non-small cell lung cancer: u-par and E-cadherin are novel biomarkers of cetuximab sensitivity[J]. Cancer Res, 2009, 69 (6) :2461-2470.

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