高三尖杉酯碱对白血病K562细胞增殖和DNA损伤相关蛋白表达的影响
柯波1 俞菊红2 涂俐嫣2 程洪波1
1.江西省人民医院血液内科,江西南昌 330006;
2.江西省人民医院医学影像科,江西南昌 330006
Effects of homoharringtonine on proliferation and DNA damage related protein expression in leukemia K562 cells
KE Bo1 YU Juhong2 TU Liyan2 CHENG Hongbo1
1.Department of Hematopathology, Jiangxi Provincial People’s Hospital, Jiangxi Province, Nanchang 330006, China;
2.Department of Medical Imaging, Jiangxi Provincial People’s Hospital, Jiangxi Province, Nanchang 330006, China
摘要 目的 研究高三尖杉酯碱(HHT)对人白血病细胞K562细胞增殖和DNA损伤及相关蛋白表达的影响。方法 体外培养人白血病K562细胞,将其分为HHT组和对照组,HHT组又分为5×10-9、1×10-8、5×10-8、1×10-7 mol/L不同浓度的HHT亚组。CCK-8方法检测不同浓度HHT对K562细胞增殖的影响;Western blot检测不同浓度的HHT对K562细胞增殖[兔抗人细胞周期蛋白D1(Cyclin D1)和兔抗人核蛋白MKI67(Ki-67)]和DNA损伤[兔抗人组蛋白H2AX的磷酸化(γ-H2AX)和磷酸化兔抗人毛细血管扩张性共济失调症突变蛋白激酶(p-ATM)]相关蛋白表达的影响。 结果 HHT对人白血病K562细胞有显著抑制作用,不同浓度(5×10-9、1×10-8、5×10-8、1×10-7 mol/L)HHT抑制率分别为(4.70±0.45)%、(9.80±0.35)%、(34.00±0.29)%和(41.00±0.64)%;与对照组比较,5×10-9、1×10-8、5×10-8、1×10-7 mol/L HHT组均可下调Cyclin D1蛋白表达,差异均有统计学意义(均P < 0.05)。与对照组比较,5×10-8、1×10-7 mol/L HHT组Ki-67蛋白表达水平明显下调,差异均有统计学意义(均P < 0.05)。与对照组比较,5×10-8、1 ×10-7 mol/L HHT组可诱导γ-H2AX蛋白的表达上调,差异均有统计学意义(均P < 0.05)。与对照组比较,1×10-8、5×10-8、1×10-7 mol/L HHT组可上调p-ATM水平,差异均有统计学意义(均P < 0.05)。 结论 HHT可通过下调增殖相关蛋白的表达抑制白血病K562细胞的增殖,并可能对细胞DNA损伤具有诱导作用。
关键词 :
高三尖杉酯碱 ,
K562细胞 ,
细胞增殖 ,
DNA损伤
Abstract :Objective To study the effects of homoharringtonine (HHT) on proliferation and DNA damage related protein expression in human leukemic K562 cells. Methods Human leukemia K562 cells were cultured in vitro, and divided into HHT group and control group. HHT group was further divided into HHT subgroups with different concentrations of 5×10-9, 1×10-8, 5×10-8 and 1×10-7 mol/L. The effects of HHT at different concentrations on the proliferation of K562 cells were detected by CCK-8 method. The effects of different HHT concentrations on K562 cells proliferation (rabbit anti human cyclin D1 [Cyclin D1] and rabbit anti human nuclear protein MKI67 [KI-67]) and the expression of DNA damage (rabbit anti human histone H2AX phosphorylation [γ-H2AX] and phosphorylated rabbit anti human ataxia telangiectasia mutated protein kinase [p-ATM]) relative protein were analyzed by Western blot. Results HHT significantly inhibited human leukemic K562 cells, with HHT inhibition rates (4.70±0.45)%, (9.80±0.35)%, (34.00±0.29)%, and (41.00±0.64)% at different concentrations (5×10-9, 1×10-8, 5×10-8 and 1×10-7 mol/L), respectively. Compared with the control group, Cyclin D1 protein expression could be down-regulated in 5×10-9, 1×10-8, 5×10-8 and 1×10-7 mol/L HHT groups, and the differences were statistically significant (all P < 0.05). Compared with the control group, Ki-67 expression levels in 5×10-8 and 1×10-7 mol/L HHT group were significantly down-regulated, with statistically significant differences (all P < 0.05). Compared with the control group, the upregulation of the expression of γ-H2AX proteins were induced in 5×10-8 and 1×10-7 mol/L HHT groups, with statistically significant differences (all P < 0.05). Compared with the control group, p-ATM levels were increased in the 1×10-8, 5×10-8 and 1×10-7 mol/L HHT groups, with statistically significant differences (all P < 0.05). Conclusion HHT can inhibit the proliferation of leukemic K562 cells by down-regulating the expression of proliferation-related proteins, and may induce cell DNA damage.
Key words :
Homoharringtonine
K562 cells
Proliferation
DNA damage
基金资助: 江西省卫生计生委中医药科研课题(2017B100);
江西省卫生计生委科技计划项目(20181005);
江西省青年科学基金资助项目(20171BAB215031)。
通讯作者:
程洪波(1973-),男,主任医师,主要从事血液疾病的诊疗及基础研究。
作者简介 : 柯波(1987-),男,硕士,主要从事血液肿瘤分子生物学研究。
[1] Quintás-Cardama A,Kantarjian H,Cortes J. Homoharringtonine,omacetaxine mepesuccinate,and chronic myeloid leukemia circa 2009 [J]. Cancer,2009,115(23):5382-5393. doi:10.1002/cncr.24601.
[2] Tan M,Zhang Q,Yuan X,et al. Synergistic killing effects of homoharringtonine and arsenic trioxide on acute myeloid leukemia stem cells and the underlying mechanisms [J]. J Exp Clin Cancer Res,2019,38(1):308. doi:10.1186/s13046-019-1295-8.
[3] Jin J,Wang JX,Chen FF,et al. Homoharringtonine-based induction regimens for patients with de-novo acute myeloid leukaemia:a multicentre,open-label,randomised,controlled phase 3 trial [J]. Lancet Oncol,2013,14(7):599-608. doi:10.1016/S1470-2045(13)70152-9.
[4] Kantarjian HM,O′Brien S,Cortes J. Homoharringtonine/Omacetaxine Mepesuccinate:The Long and Winding Road to Food and Drug Administration Approval [J]. Clin Lymphoma Myeloma Leuk,2013,13(5):530-533. doi:10.1016/j.clml.2013.03.017.
[5] Kuroda J,Kamitsuji Y,Kimura S,et al. Anti-myeloma effect of homoharringtonine with concomitant targeting of the myeloma-promoting molecules,Mcl-1,XIAP,and beta-catenin [J]. Int J Hematol,2008,87(5):507-515. doi:10.1007/s12185-008-0081-8.
[6] Chen J,Mu QT,Li X,et al. Homoharringtonine targets Smad3 and TGF-β pathway to inhibit the proliferation of acute myeloid leukemia cells [J]. Oncotarget,2017,8(25):40318-40326. doi:10.18632/oncotarget.16956.
[7] Gandhi V,Plunkett W,Cortes JE. Omacetaxine:a protein translation inhibitor for treatment of chronic myelogenous leukemia [J]. Clin Cancer Res,2014,20(7):1735-1740. doi:10.1158/1078-0432.CCR-13-1283.
[8] Bohlander SK. A new kid on the block for acute myeloid leukemia treatment? Homoharringtonine interferes with key pathways in acute myeloid leukemia cells [J]. Haematologica,2020,105(1):7-9. doi:10.3324/haematol.2019. 234880.
[9] Li CY,Dong L,Su R,et al. Homoharringtonine exhibits potent anti-tumor effect and modulates DNA epigenome in acute myeloid leukemia by targeting SP1/TET1/5hmC [J]. Haematologica,2020,105(1):148-160. doi:10.3324/haematol.2018.208835.
[10] 中华医学会血液学分会白血病淋巴瘤学组.成人急性髓系白血病(非急性早幼粒细胞白血病)中国诊疗指南(2017年版)[J].中华血液学杂志,2017,38(3):177-182. doi:10.3760/cma.j.issn.0253-2727.2017.03.001.
[11] 谢瑜,谭琳,吴迪.HAG方案治疗老年低增生性急性髓系白血病20例疗效观察[J].中国医药导报,2010,33:148-149. doi:CNKI:SUN:YYCY.0.2010-33-099.
[12] Lou YJ,Qian WB,Jin J. Homoharringtonine induces apoptosis and growth arrest in human myeloma cells [J]. Leuk Lymphoma,2007,48(7):1400-1406. doi:10.1080/10428 190701411466.
[13] 丁亦含,吴晶晶,王倩,等.高三尖杉酯碱通过mTOR通路诱导慢性髓系白血病K562细胞凋亡[J].中国实验血液学杂志,2018,26(1):105-109. doi:10.7534/j.issn.1009-2137.2018.01.017.
[14] Li S,Bo ZL,Jiang Y,et al. Homoharringtonine promotes BCR-ABL degradation through the p62-mediated autophagy pathway [J]. Oncol. Rep.,2020,43(1):113-120. doi:10.3892/or.2019.7412.
[15] Ke B,Jin CH,Liu HY,et al. Homoharringtonine enhances idarubicin-induced apoptosis via regulation of the mitochondrial pathway [J]. Int J Clin Exp Med,2019,12(2):1503-1513.
[16] Du ZY,Tong XM,Ye X. Cyclin D1 promotes cell cycle progression through enhancing NDR1/2 kinase activity independent of cyclin-dependent kinase 4 [J]. J Biol Chem,2013,288(37):26678-26687. doi:10.1074/jbc.M113. 466433.
[17] Siddiqui MS,Fran?觭ois M,Fenech MF,et al. Persistent γH2AX:A promising molecular marker of DNA damage and aging [J]. Mutat Res Rev Mutat Res,2015,766:1-19. doi:10.1016/j.mrrev.2015.07.001.
[18] Nagelkerke A,Span PN. Staining Against Phospho-H2AX (γ-H2AX) as a Marker for DNA Damage and Genomic Instability in Cancer Tissues and Cells [J]. Adv Exp Med Biol,2016,899:1-10. doi:10.1007/978-3-319-26666-4_1.
[19] Wakasugi M,Sasaki T,Matsumoto M,et al. Nucleotide excision repair-dependent DNA double-strand break formation and ATM signaling activation in mammalian quiescent cells [J]. J Biol Chem,2014,289(41):28730-28737. doi:10.1074/jbc.M114.589747.
[20] Guo QQ,Wang SS,Zhang SS,et al. ATM-CHK2-Beclin 1 axis promotes autophagy to maintain ROS homeostasis under oxidative stress [J]. EMBO J,2020,39(10):e103111. doi:10.15252/embj.2019103111.
[21] Popp HD,Kohl V,Naumann N,et al. DNA Damage and DNA Damage Response in Chronic Myeloid Leukemia [J]. Int J Mol Sci,2020,21(4):1177. doi:10.3390/ijms21041177.
[22] Xu RD,Yu SY,Zhu D,et al. hCINAP regulates the DNA-damage response and mediates the resistance of acute myelocytic leukemia cells to therapy [J]. Nat Commun,2019,10(1):3812. doi:10.1038/s41467-019-11795-5.
[23] Wu JJ,Wei B,Shi YY,et al. Homoharringtonine enhances the effect of imatinib on chronic myelogenous leukemia cells by downregulating ZFX [J]. Mol Med Rep,2019,20(4):3233-3239. doi:10.3892/mmr.2019.10539.
[24] Chen J,Mu Q,Li X,et al. Homoharringtonine targets Smad3 and TGF-β pathway to inhibit the proliferation of acute myeloid leukemia cells [J]. Oncotarget,2017,8(25):40318-40326. doi:10.18632/oncotarget.16956.
[25] Cao W,Liu Y,Zhang R,et al. Homoharringtonine induces apoptosis and inhibits STAT3 via IL-6/JAK1/STAT3 signal pathway in Gefitinib-resistant lung cancer cells [J]. Sci Rep,2015,5:8477. doi:10.1038/srep08477.
[26] Chen XJ,Zhang WN,Chen B,et al. MYCHomoharringtonine deregulates transcriptional expression by directly bin-ding NF-κB repressing factor [J]. Proc Natl Acad Sci U S A,2019,116(6):2220-2225. doi:10.1073/pnas.1818539116.
[1]
蔡路兵 翟梅娟 陈晓丹. P16、Ki-67表达与直肠癌患者预后的关系 [J]. 中国医药导报, 2020, 17(23): 24-27.
[2]
郭小叶 冒平 王佳 廉海平 王伟 白晓斌 宋锦宁. miR-361-3p调节恶性胶质瘤细胞功能的研究 [J]. 中国医药导报, 2019, 16(28): 7-11.
[3]
程亚玉1 谭雪莹2 黄飞2 张萍3 . Galectin-9蛋白过表达对卵巢癌细胞增殖、迁移及凋亡的影响 [J]. 中国医药导报, 2018, 15(3): 13-16.
[4]
王瑾 马肖容▲ 张王刚. CCK-8法在淋巴细胞增殖检测中最佳实验条件的筛选 [J]. 中国医药导报, 2018, 15(23): 13-16.
[5]
罗海恩 毛新展. NF-κB p65基因沉默对类风湿性关节炎滑膜细胞增殖凋亡的影响 [J]. 中国医药导报, 2017, 14(35): 8-11.
[6]
齐彦 廖斌 徐成波 皇甫真萍 陈佳薇. 细胞氧化-还原状态影响贝母素甲对人白血病细胞K562细胞增殖的抑制 [J]. 中国医药导报, 2017, 14(18): 16-19.
[7]
钱亚芳1,2 单乐天3 金红婷3 谷满仓2. 补肾活血方亲脂性组分的气相色谱分析及诱导成骨细胞分化研究 [J]. 中国医药导报, 2017, 14(17): 8-11.