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Gankyrin基因沉默对人卵巢癌SKOV3/CDDP细胞顺铂耐药性的逆转作用和机制 被引量:7

The effects and mechanisms of Gankyrin silencing on reversing the cisplatin resistance of human ovarian cancer SKOV3/DDP cell line
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摘要 背景与目的:卵巢癌是常见的妇科肿瘤,抗肿瘤药耐药性的产生是卵巢癌治疗失败的主要原因之一,Gankyrin基因被认为与肿瘤耐药性密切相关,本文探讨了Gankyrin基因沉默对卵巢癌耐顺铂细胞系SKOV3/DDP顺铂耐药性的逆转作用及机制。方法:应用real-time PCR技术考察Gankyrin在SKOV3和SKOV3/DDP细胞中的表达,应用MTS法检测Gankyrin对SKOV3/DDP细胞顺铂耐受性的影响,应用流式细胞术检测肿瘤细胞凋亡和细胞内罗丹明-123(Rhodamine-123,Rh-123)含量的变化,Western blot和real-time PCR技术检测肿瘤细胞耐药相关蛋白MDR1、Caspase-3/8、Survivin和Bcl-2蛋白表达,Western blot法检测p53、NF-κB和PTEN蛋白表达和AKT磷酸化水平。结果:Gankyrin在SKOV3/DDP细胞中表达升高,沉默Gankyrin基因后可增加SKOV3/DDP细胞对顺铂的敏感性。基因沉默前后耐药逆转倍数(resistant factor,RF)为1.81和2.45,肿瘤细胞中Rh-123含量提高了1.73和2.42倍,细胞凋亡率是对照组的2.23倍和4.23倍,耐药相关蛋白MDR1、Survivin和Bcl-2蛋白水平显著下降,MDR1 mRNA表达是对照组的62.8%和21.6%,Survivin mRNA表达是对照组的24.5%和10.3%,Bcl-2 mRNA表达是对照组的47.5%和18.4%,Caspase-3/8、p53和PTEN表达水平上升,AKT磷酸化和NF-κB水平下降。结论:沉默Gankyrin基因可逆转SKOV3/DDP对顺铂的耐药性,可能与抑制药物外排,促进细胞凋亡有关,PTEN/AKT/NF-κB/p53信号通路可能是其中心环节。 Background and purpose: Ovarian cancer is the common gynecological cancer, and the drug resistance of anti-tumor drug was one of major reasons for therapy failure, some studies considered that there is a closed relationship between Gankyrin and drug resistance. In this study, we investigated the effects and mechanisms of Gankyrin silencing on reversing the cisplatin resistance of ovarian cancer drug-resistant SKOV3/DDP cell line. Methods: The expression of Gankyrin in SKOV3 and SKOV3/DDP cells was measured by real-time PCR assay, MTS assay was employed to determine the effect of Gankyrin on SKOV3/DDP sensitivity to cisplatin, apoptosis rate and intracellular concentration of rhodamine-123 (Rh-123) were determined by flow cytometry, the expression of multi- drugs resistant protein MDR1, Caspase-3/8, Survivin and Bcl-2 were determined by Western blot and real-time PCR. The phosphorylation of AKT and expression of p53, NF-rd3 and PTEN were analyzed by Western blot assay. Results: The expression of Gankyrin was increased in SKOV3/DDP cells, Gankyrin silencing was able to increase the cisplatin sensitivity of SKOV3/DDP. Before and after gene silencing, the reverse folds (RF) to cisplatin were 1.81 and 2.45, respectively, the intracellular levels of Rh-123 were 1.73 and 2.42 fold, the apoptosis rates were 2.23 and 4.23 fold,the expressions of MDR1, Survivin and Bcl-2 were downregulated, the mRNA expressions of MDR1 were 62.8% and 21.6%, the mRNA expressions of Survivin were 24.5% and 10.3%, the mRNA expressions of Bcl-2 were 47.5% and 18.4%, the levels of Caspase-3/8, p53 and PTEN were elevated, phosphorylation of AKT and expression of NF-kB were downregulated compared with control group. Conclusion: Gankyrin silencing was able to reverse the cisplatin resistance of SKOV3/DDP cells by inhibiting the drug efflux and promoting cell apoptosis, the PTEN/AKT/NF-κB/p53 may be the key pathway.
作者 王倩 程堃
出处 《中国癌症杂志》 CAS CSCD 北大核心 2014年第1期35-40,共6页 China Oncology
关键词 Gankyrin基因 卵巢癌 顺铂耐药 Gankyrin gene Ovarian cancer Cisplatin resistant
作者简介 通信作者:王倩E—mail:wangqian_sgh@126.com
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参考文献12

  • 1FURUKAWA S, SOEDA S, KIKO Y, et al. MCP-I promotes invasion and adhesion of human ovarian cancer cells [ J ] . Antieancer Res, 2013, 33(11): 4785-4790.
  • 2YUNOS N M, MUTALIP S S, JAURI M H, et al. Anti- proliferative and prn-apoptotic effects from sequenced combinations of andrographolide and cisplatin on ovarian cancer cell lines [ J ] . Anticancer Res, 2013, 33(10): 4365- 4371.
  • 3SONG X, WANG J, ZHENG T, et al. LBH589 inhibits proliferation and metastasis of hepatocellular carcinoma via inhibition of gankyrin/STAT3/Akt pathway [ J ] . Mnl Cancer, 2013, 12(1): 114.
  • 4RABIK C A, DOLAN M E. Molecular mechanisms of resistance and toxicity associated with platinating agents [ J ]. Cancer Treat Rev, 2007, 33(1): 9-23.
  • 5KEPPLER D. Multidmg resistance proteins (MRPs, ABCCs): importance for pathophysiology and drug therapy [ J ] . Handh Exp Pharmacok 2011, (201): 299-323.
  • 6HOROWITZ J C, AJAYI I O, KULASEKARAN P, et al. Survivin expression induced hy endothelin-1 promotes myofibroblast resistance to apoptosis [ J ] .lnt J Biochem Cell Biol, 2012, 44(1): 158-169.
  • 7WU S, LIU B, ZHANG Q, et al. Dihydromyricetin reduced Bcl-2 expression via p53 in human hepatoma hepG2 cells [ J ] . PLoS One, 2013, 8(11): e76886.
  • 8ALVAREZ-GONZALEZ R, MENDOZA-ALVAREZ H, FREY M, et al. Up-regulation of two distinct p53-DNA binding functions by covalent poly(ADP-ribosyl)ation: transactivating and single strand break sensing [ J ] . Cancer Invest, 2013, 31(9): 563-570.
  • 9LIU J, LI J, ZHANG J F, et al. Combination of fenretinide and selenite inhibits proliferation and induces apoptosis in ovarian cancer cells [ J ]. Int J Mol Sci, 2013, 14(11): 21790-21804.
  • 10MATSUDA S, NAKANISHI A, WADA Y, et al. Roles of PI3K/ AKT/PTEN pathway as a target for pharmaceutical therapy [J]. Open Med Chem J, 2013, 7: 23-29.

二级参考文献16

  • 1金正均.合并用药中的相加[J].中国药理学报,1980,1:70-73.
  • 2JEMAL A,SIEGEL R,XU J,et al.Cancer statistics,2010[J].CA Cancer J Clin,2010,60(5):277-300.
  • 3CARNERO A.The PKB/AKT pathway in cancer[J].Curr Pharm Des,2010,16(1):34-44.
  • 4MANNING B D,CANTLEY L C.AKT/PKB signaling:Navigating downstream[J].Cell,2007,129(7):261-1274.
  • 5CHING C B,HANSEL D E,et al.Expanding therapeutic targets in bladder cancer:the PI3K/Akt/mTOR pathway[J].Lab Invest,2010,90(10):1406-1414.
  • 6TOKUNAGA E,KIMURA Y,MASHINO K,et al.Activation of P13K/Akt signaling and hormone resistance in breast cancer[J].Breast Cancer,2006,13(2):137-144.
  • 7PEREZ-TENORIO G,STAL O.Southeast Sweden Breast Cancer Group.Activation of AKT/PKB in breast cancer predicts a worse outcome among endocrine treated patients[J].Br J Cancer,2002,86(4):540-545.
  • 8EVANGELISTI C,RICCI F,TAZZARI P,et al.Preclinical testing of the Akt inhibitor triciribine in T-cell acute lymphoblastic leukemia[J].J Cell Physiol,2011,226(3):822-831.
  • 9YAP T A,WALTON M I,HUNTER L J,et al.Preclinical pharmacology,antitumor activity,and development of pharmacodynamic markers for the novel,potent AKT inhibitor CCT128930[J].Mol Cancer Ther,2011,10(2):360-371.
  • 10ELROD H A,LIN Y D,YUE P,et al.The alkylphospholipid perifosine induces apoptosis of human lung cancer cells requiring inhibition of Akt and activation of the extrinsic apoptotic pathway[J].Mol Cancer Ther,2007,6(7):2029-2038.

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