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小豆蔻明诱导K562细胞凋亡及其相关凋亡蛋白的表达 被引量:1

Cardamonin induces apoptosis and expression of apoptosis-related proteins in K562 cells
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摘要 目的探讨小豆蔻明诱导K562细胞凋亡与PTEN、p-Akt、NF-κB、Bcl-2等抑凋亡蛋白及促凋亡蛋白表达量的关系。方法 1普通光镜观察小豆蔻明作用K562细胞48 h后的细胞形态学变化。2采用MTT法检测小豆蔻明作用K562细胞48 h后的凋亡情况,计算IC50。3应用流式细胞仪检测小豆蔻明作用K562细胞48 h后的细胞凋亡率。4采用RT-PCR技术检测小豆蔻明作用K562细胞48 h后Bcl-2、Bax的mRNA表达量。5采用Western blot技术检测小豆蔻明作用K562细胞48 h后PTEN、p-Akt、NF-κB、Bcl-2的蛋白表达量。结果小豆蔻明作用K562细胞48 h后,形态学出现明显凋亡现象。MTT提示K562细胞增殖抑制明显且呈量效和时效关系。早期凋亡率与空白组比有显著增加(P<0.05),呈剂量依赖关系。Bcl-2 mRNA的表达较空白组明显下降(P<0.05),Bax mRNA的表达较空白组明显升高(P<0.05),呈现浓度依赖性。PTEN蛋白表达量随小豆蔻明的浓度增加明显增加,而p-Akt、NF-κB、Bcl-2蛋白表达量则减少。结论小豆蔻明通过增加PTEN蛋白的表达量,同时下调p-Akt、NF-κB、Bcl-2蛋白的表达量促进K562细胞的凋亡,且呈剂量依赖性。 ObjectiveTo observe the apoptotic effect of cardamonin on K562 cells and its relationship with the expressions of PTEN, p-Akt, NF-κB and Bcl-2.Methods K562 cells were treated with cardamonin for 48 h, and the following tests were performed:(1) The cell morphology was observed by light microscopy.(2)IC50 of the K562 cells was dtermined by MTT test.(3) The apoptosis rate was detected by flow cytometry.(4) The expressions of Bcl-2 and Bax mRNA were detected a by RT-PCR.(5) The expressions of PTEN, p-Akt, NF-κB and Bcl-2 proteins were detected by Western blot.Results Obvious apoptosis was observed in the K562 cells after treated with cardamonin for 48 h.MTT assay indicated that the proliferation of K562 cells was obviously inhibited in a dose-and time-dependent manner. Comparing with the blank group, the early apoptosis rate and expression of Bax mRNA were significantly increased.At the same time, the expression of Bcl-2 mRNA was significantly decreased.All of them presented a dose-dependent manner. The expression of PTEN obviously increased with the increasing dose of cardamonin and the expressions of p-Akt, NF-κB and Bcl-2 were decreased.Conclusions Cardamonin promotes the apoptosis in K562 cells in a dose-dependent manner by increasing the expression of PTEN and decreasing the expressions of p-Akt, NF-κB, and Bcl-2.
出处 《中国比较医学杂志》 CAS 2014年第10期7-11,17,共6页 Chinese Journal of Comparative Medicine
基金 浙江省医药卫生一般研究计划(2012KYB136) 浙江省大学生科技创新活动计划资助项目(2012 R410057)
关键词 小豆蔻明 K562细胞 凋亡 PTEN P-AKT NF-κB BCL-2 Cardamonin K562 cells Apoptosis, PTEN, p-Akt, NF-κB, Bcl-2
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  • 1Yamamoto N, Kawabata K, Sawada K, et al. Cardamonin stimulates glucose uptake through translocation of glucose transporter-4 in L6 myotubes [ J]. Pyhtother Res, 2011, 25 (8) : 1218 -1224.
  • 2Fusi F, Cavalli M, Mulholland D, et al. Cardamonin is a bifunctional vasodilator that inhibits Ca (v) 1.2 current and stimu}ates K(Ca) 1.1 current in rat tail artery myocytes [J] . Pharmacol Exp Ther, 2010, 332(2) :531 -540.
  • 3Hatziieremia S, Gray AI, Ferro VA, et al. The effects of eardamonin on lipopolysaeeharide-induced inflammatory protein production and MAP kinase and NFkappaB signalling pathways in monocytes/macrophages[J]. Br J Pharmacol, 2006, 149 (2) : 188 - 198.
  • 4Park MK, Seung HJ, Lee HJ, et al. Novel suppressive effects of eardamonin on the activity and expression of transglutaminase-2 lead to blocking the migration and invasion of cancer cells [ J]. Life Sci, 2013, 92(2) :154 -160.
  • 5Hyeonseok K, Young-J K, Evangeline CA, et al. Induction of autophagy by dimethyl eardamonin is associated with proliferative arrest in human eolorectal carcinoma HCTll6 and LOVO ceils [J]. J Cellular Biochem, 2011, 112(9) :2471 -2479.
  • 6Yadav VR, Prasad S, Aggarwal BB, et al. Cardamonin sensitizes tumour cells to TRAIL through ROS- and CHOP-mediated up- regulation of death receptors and down-regulation of survival proteins [ J J. Br J Pharmaeol, 2012, 165 (3) : 741 - 753.
  • 7Monticl-DC, Cordeu L, Agirre X, et al. Resistance to imatinib mesylate-induced apoptosis in acute lymphoblastic leukemia is associated with PTEN down regulation due to promoter hypermethylation [ J]. Leuk Res, 2008, 32 (5): 709- 716.
  • 8Omer HY, Valdez R, Brian KT, et al. Pten dependence distinguishes haematopoietic stem cells from leukaemia-initiating ceils [J]. Nature, 2006, 441(7092):475-482.
  • 9He WY, Jiang Y, Zhang XB, et al. Anticancer cardamonin analogs suppress the activation of NF-kappaB pathway in lung cancer cells [J]. Mol Cell Biochem 2014, 389(1 -2): 25 -33.
  • 10Sawa H, Kobayashi T, Mukai K, et al. Bax overexpression enhances cytochrome c release from mitochondrla and sensitizes KATOⅢ gastric cancer cells to chemotherapeutic agent-induced apoptosis [J]. Int J Oncol, 2000, 16(4):745-754.

二级参考文献25

  • 1汪圣毅,王玉琦,符伟国,刘康达,刘弋.人脐带动脉平滑肌细胞的培养及纯化[J].安徽医科大学学报,2007,42(2):231-233. 被引量:4
  • 2Lee E S, Lee J O, Lee S K, et al. Caffeic acid phenethyl ester accumulates beta-catenin through GSK-3beta and participates in proliferation through mTOR in C2C12 cells[J]. Life Sci, 2009, 84 (21/22) : 755.
  • 3Patursky-Polischuk I, Stolovich-Rain M, Hausner-Hano chi M, et al. The TSC-mTOR pathway mediates translational activation of TOP mRNAs by insulin largely in a raptor- or rietor-independent manner[J]. Mol Cell Biol, 2009, 29 (3) : 640.
  • 4Wang Z T, Lau C W, Chan F L, et al. Vasorelaxant effects of cardamonin and alpinetin from Alpinia henryi K. Schum[ J]. J Cardiovasc Pharmacol, 2001, 37 (5): 596.
  • 5Rashid F, Ahmed R, Mahmood A, et al. Flavonoid glycosides from Prunus armeniaca and the antibacterial activity of a crude extract[J]. Arch Pharm Res, 2007, 30 (8) : 932.
  • 6Meshkani R, Adeli K. Hepatic insulin resistance, metabolic syn- drome and cardiovascular disease [ J ]. Clin Biochem, 2009, 42 (13/14) : 1331.
  • 7Lorenzo C, Wagenknecht L E, DAgostino R B, et al. Insulin resistance, beta-cell dysfunction, and conversion to type 2 diabetes in a multiethnic population : The insulin resistance atheroselerosis study[J]. Diabetes Care, 2010, 33 (1) : 67.
  • 8Cifarelli V, Luppi P, Tse H M, et al. Human proinsulin C-peptide reduces high glucose-induced proliferation and NF-kappaB activation in vascular smooth muscle cells [ J ]. Atherosclerosis, 2008, 201 (2) : 248.
  • 9Rufino M, Hemandez D, Barrios Y, et al. The GLUT-1 XbaI gene polymorphism is associated with vascular calcifications in nondiabetic uremic patients[ J]. Nephmn Clin Pract, 2008, 108 (3) : c182.
  • 10Mussig K, Fiedler H, Staiger H, et al. Insulin-induced stimulation of JNK and the PI 3-kinase/mTOR pathway leads to phosphorylation of serine 318 of IRS-1 in C2C12 myotubes[ J]. Biochem Biophys Res Commun, 2005, 335 (3) : 819.

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