国际肿瘤学杂志››2016,Vol. 43››Issue (2): 116-.
李楠, 蒋大明, 刘双萍
出版日期:
2016-02-08发布日期:
2015-12-28LI Nan, JIANG Da-Ming, LIU Shuang-Ping
Online:
2016-02-08Published:
2015-12-28摘要:细胞核内组蛋白乙酰化与去乙酰化失衡可诱发肿瘤。组蛋白去乙酰化酶(HDAC)作用于组蛋白,使其去乙酰化,维系组蛋白乙酰化与去乙酰化的平衡状态,与癌相关基因转录表达、细胞增殖分化及细胞凋亡等过程密切相关。HDAC抑制剂目前是国内外研究的热点,已有十多种HDAC抑制剂用于治疗血液肿瘤和恶性实体瘤,表现出明显的抗肿瘤活性。
李楠, 蒋大明, 刘双萍. 以组蛋白去乙酰化酶为靶点的抗肿瘤研究[J]. 国际肿瘤学杂志, 2016, 43(2): 116-.
LI Nan, JIANG Da-Ming, LIU Shuang-Ping. Research on histone deacetylase as a target for anticancer therapy[J]. Journal of International Oncology, 2016, 43(2): 116-.
[1] Yang R, Wu Y, Wang M, et al. HDAC9 promotes glioblastoma growth via TAZmediated EGFR pathway activation[J]. Oncotarget, 2015, 6(10): 76447656. [2] Damaskos C, Karatzas T, Nikolidakis L, et al. Histone deacetylase (HDAC) inhibitors: current evidence for therapeutic activities in pancreatic cancer[J]. Anticancer Res, 2015, 35(6): 31293135. [3] Koeneke E, Witt O, Oehme I. HDAC family members intertwined in the regulation of autophagy: a druggable vulnerability in aggressive tumor entities[J]. Cells, 2015, 4(2): 135168. DOI:10.3390/cells4020135. [4] Herr MJ, Longhurst CM, Baker B, et al. Tetraspanin CD9 modulates human lymphoma cellular proliferation via histone deacetylase activity[J]. Biochem Biophys Res Commun, 2014, 447(4): 616620. DOI:10.1016/j.bbrc.2014.04.046. [5] Ding G, Liu HD, Huang Q, et al. HDAC6 promotes hepatocellular carcinoma progression by inhibiting P53 transcriptional activity[J]. FEBS Lett, 2013, 587(7): 880886. DOI:10.1016/j.febslet.2013.02.001. [6] Seo J, Min SK, Park HR, et al. Expression of histone deacetylases HDAC1, HDAC2, HDAC3, and HDAC6 in invasive ductal carcinomas of the breast[J]. J Breast Cancer, 2014, 17(4): 323331. DOI:10.4048/jbc.2014.17.4.323. [7] Chen MC, Chen CH, Wang JC, et al. The HDAC inhibitor, MPT0E028, enhances erlotinibinduced cell death in EGFRTKIresistant NSCLC cells[J]. Cell Death Dis, 2013, 4: e810. DOI:10.1038/cddis.2013.330. [8] Liu J, Edagawa M, Goshima H, et al. Role of ATF3 in synergistic cancer cell killing by a combination of HDAC inhibitors and agonistic antiDR5 antibody through ER stress in human colon cancer cells[J]. Biochem Biophys Res Commun, 2014, 445(2): 320326. DOI:10.1016/j.bbrc.2014.01.184. [9] Zhao B, He T. Chidamide, a histone deacetylase inhibitor, functions as a tumor inhibitor by modulating the ratio of Bax/Bcl2 and P21 in pancreatic cancer[J]. Oncol Rep, 2015, 33(1): 304310. DOI:10.3892/or.2014.3595. [10] Jin JS, Tsao TY, Sun PC, et al. SAHA inhibits the growth of colon tumors by decreasing histone deacetylase and the expression of cyclin D1 and survivin[J]. Pathol Oncol Res, 2012, 18(3): 713720. DOI:10.1007/s1225301294997. [11] Noh EJ, Lim DS, Jeong G, et al. An HDAC inhibitor, trichostatin A, induces a delay at G2/M transition, slippage of spindle checkpoint, and cell death in a transcriptiondependent manner[J]. Biochem Biophys Res Commun, 2009, 378(3): 326331. DOI:10.1016/j.bbrc.2008.11.057. [12] Yang B, Yu D, Liu J, et al. Antitumor activity of SAHA, a novel histone deacetylase inhibitor, against murine B cell lymphoma A20 cells in vitro and in vivo[J]. Tumour Biol, 2015, 36(7): 50515061. DOI:10.1007/s1327701531561. [13] Bae HJ, Jung KH, Eun JW, et al. MicroRNA221 governs tumor suppressor HDAC6 to potentiate malignant progression of liver cancer[J]. J Hepatol, 2015, 63(2): 408419. DOI:10.1016/j.jhep.2015.03.019. [14] Qiao Z, Ren S, Li W, et al. Chidamide, a novel histone deacetylase inhibitor, synergistically enhances gemcitabine cytotoxicity in pancreatic cancer cells[J]. Biochem Biophys Res Commun, 2013, 434(1): 95101. DOI:10.1016/j.bbrc.2013.03.059. [15] Dong M, Ning ZQ, Xing PY, et al. Phase Ⅰ study of chidamide (CS055/HBI8000), a new histone deacetylase inhibitor, in patients with advanced solid tumors and lymphomas[J]. Cancer Chemother Pharmacol, 2012, 69(6): 14131422. DOI:10.1007/s0028001218475. [16] Mahalingam D, Mita M, Sarantopoulos J, et al. Combined autophagy and HDAC inhibition: a phase Ⅰ safety, tolerability, pharmacokinetic, and pharmacodynamic analysis of hydroxychloroquine in combination with the HDAC inhibitor vorinostat in patients with advanced solid tumors[J]. Autophagy, 2014, 10(8): 14031414. DOI:10.4161/auto.29231. [17] Prince HM, Dickinson M. Romidepsin for cutaneous Tcell lymphoma[J]. Clin Cancer Res, 2012, 18(13): 35093515. DOI:10.1158/10780432.CCR113144. |
[1] | 刘娜, 寇介丽, 杨枫, 刘桃桃, 李丹萍, 韩君蕊, 杨立洲.血清miR-106b-5p、miR-760联合低剂量螺旋CT诊断早期肺癌的临床价值[J]. 国际肿瘤学杂志, 2024, 51(6): 321-325. |
[2] | 杨蜜, 别俊, 张加勇, 邓佳秀, 唐组阁, 卢俊.局部晚期可切除食管癌新辅助治疗疗效及预后分析[J]. 国际肿瘤学杂志, 2024, 51(6): 332-337. |
[3] | 袁健, 黄燕华.Hp-IgG抗体联合血清DKK1、sB7-H3对早期胃癌的诊断价值[J]. 国际肿瘤学杂志, 2024, 51(6): 338-343. |
[4] | 陈红健, 张素青.血清miR-24-3p、H2AFX与肝癌患者临床病理特征及术后复发的关系研究[J]. 国际肿瘤学杂志, 2024, 51(6): 344-349. |
[5] | 郭泽浩, 张俊旺.PFDN及其亚基在肿瘤发生发展中的作用[J]. 国际肿瘤学杂志, 2024, 51(6): 350-353. |
[6] | 张百红, 岳红云.新作用机制的抗肿瘤药物进展[J]. 国际肿瘤学杂志, 2024, 51(6): 354-358. |
[7] | 许凤琳, 吴刚.EBV在鼻咽癌肿瘤免疫微环境和免疫治疗中的研究进展[J]. 国际肿瘤学杂志, 2024, 51(6): 359-363. |
[8] | 王盈, 刘楠, 郭兵.抗体药物偶联物在转移性乳腺癌治疗中的研究进展[J]. 国际肿瘤学杂志, 2024, 51(6): 364-369. |
[9] | 张蕊, 褚衍六.基于FIT与肠道菌群的结直肠癌风险评估模型的研究进展[J]. 国际肿瘤学杂志, 2024, 51(6): 370-375. |
[10] | 高凡, 王萍, 杜超, 褚衍六.肠道菌群与结直肠癌非手术治疗的相关研究进展[J]. 国际肿瘤学杂志, 2024, 51(6): 376-381. |
[11] | 王丽, 刘志华, 杨伟洪, 蒋凤莲, 李全泳, 宋浩杰, 鞠文东.ROS1突变肺腺鳞癌合并脑梗死为主要表现的Trousseau综合征1例[J]. 国际肿瘤学杂志, 2024, 51(6): 382-384. |
[12] | 刘静, 刘芹, 黄梅.基于SMOTE算法的食管癌放化疗患者肺部感染的预后模型构建[J]. 国际肿瘤学杂志, 2024, 51(5): 267-273. |
[13] | 杨琳, 路宁, 温华, 张明鑫, 朱琳.炎症负荷指数与胃癌临床关系研究[J]. 国际肿瘤学杂志, 2024, 51(5): 274-279. |
[14] | 王俊毅, 洪楷彬, 纪荣佳, 陈大朝.癌结节对结直肠癌根治性切除术后肝转移的影响[J]. 国际肿瘤学杂志, 2024, 51(5): 280-285. |
[15] | 张宁宁, 杨哲, 檀丽梅, 李振宁, 王迪, 魏永志.宫颈细胞DNA倍体分析联合B7-H4和PKCδ对宫颈癌的诊断价值[J]. 国际肿瘤学杂志, 2024, 51(5): 286-291. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||