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腺病毒介导hIL-24基因对瘢痕疙瘩表达Bcl-2等细胞因子的影响 被引量:2

Effects of recombinant adenovirus-mediated human Interleukin-24 gene on expression of Bcl-2,IL-6 and TGF-β_1 of keloids
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摘要 目的:研究重组腺病毒介导hIL-24基因对瘢痕疙瘩成纤维细胞表达Bcl-2、IL-6和TGF-β1的影响,探讨IL-24基因对瘢痕疙瘩的生物学作用。方法:体外培养人正常皮肤及瘢痕疙瘩成纤维细胞,用含有hIL-24基因的腺病毒载体感染瘢痕疙瘩成纤维细胞,应用双抗体夹心酶联免疫吸附试验(ABC-ELISA)检测人正常皮肤及瘢痕疙瘩成纤维细胞中的Bcl-2、IL-6和TGF-β1的表达水平。结果:瘢痕疙瘩组的Bcl-2、IL-6和TGF-β1表达水平明显高于正常皮肤组;瘢痕疙瘩感染Ad.IL-24组的Bcl-2、IL-6和TGF-β1表达水平都低于腺病毒空载体组和瘢痕疙瘩组。结论:IL-24基因可抑制瘢痕疙瘩成纤维细胞表达Bcl-2、IL-6和TGF-β1。 Objective Previous studies have shown that IL-24 as a candidate of tumor suppressor gene has tumorsuppressor activity in a broad spectrum of human cancer cells both in vitro and in vivo. In this study, we investigate the effects of recombinant adenovirus-mediated human interleukin-24 gene on expression of Bcl-2, IL-6 and TGF-β1 of kelcid fibroblasts, and the biological role of human IL-24 gene in keloids, to provide a basic theory for gene therapy of keloids. Methods Fibroblasts isolated from human normal skin and keloids were cultured in DMEM medium with 10% fetal bovine serum for 24, 48, 72 hours. The expression levels of BcI-2, IL-6 and TGF-β1 in the supernatants were detected by ABC (avidin-biotin-peroxidase complex)-ELISA. Results At different times, the expression levels of Bcl- 2,1L-6 and TGF-β1 in the supernatants from keloids group were higher than human normal skin group obviously; the expression levels of Bcl-2, IL-6 and TGF-β1 in the supernatants from keloids infected Ad.lL-24 group were lower than keloids infected Ad.GFP group and keloids group. Conclusions Human IL-24 gene can inhibit expression of Bcl-2, IL-6 and TGF-β1 of cultured keliod fibroblasts.
出处 《中国美容医学》 CAS 2009年第7期970-973,共4页 Chinese Journal of Aesthetic Medicine
基金 广东省自然科学基金资助项目(编号:06028957)
关键词 IL-24基因 瘢痕疙瘩 Bcl—2 IL-6 TGF-Β1 IL-24 gene keloid BcI-2 IL-6 TGF-β1
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参考文献15

  • 1Jiang H,Lin JJ,Su ZZ,et al.Subtraction hybridization identifies a novel melanoma differentiation associated gene,mda-7,modulated during human melanoma differentiation,growth and progression [J].Oncogene,1995,11:2477-2486.
  • 2Mhashilkar AM,Schrock RD,Hindi M,et al.Melanoma differentiat ion associated gene-7 (mda-7):a novel anti-tumor gene for cancer gene therapy [J].Mol Med,2001,7:271-782.
  • 3梁杰,李建赤,罗少军,张培华,彭智,李平.增生性瘢痕组织内IL-24基因mRNA的表达及意义[J].广东医学院学报,2007,25(2):123-125. 被引量:5
  • 4李建赤,梁杰,罗少军,张培华,彭智,李平.人白细胞介素24mRNA在瘢痕疙瘩中的表达及意义[J].中国组织工程研究与临床康复,2007,11(32):6432-6435. 被引量:6
  • 5梁杰,何海填,彭智,银桂彬,罗少军.人白介素24基因重组腺病毒载体的构建与鉴定[J].中国实用医药,2007,2(33):46-48. 被引量:2
  • 6王春梅,百束比古,张启旭,严笠,中泽南堂.瘢痕疙瘩成纤维细胞的基因组学研究[J].中华整形外科杂志,2005,21(4):299-301. 被引量:28
  • 7Reed JC.Bcl-2 and the regulation of programmed cell death [J].Cell Boil,1994,124:1-15.
  • 8Park JR,Hockanbery DM.Bcl-2,a novel regulator of apoptosis [J].Cell Bioehem,1996,60:12.
  • 9Oltvai ZN,Milliman CL,Losmeger SJ.Bcl-2 heterodimerizes in vivo with a conserved homology,Bax,that accelerates Programmed cell death [J].Cell,1993,74:609-620.
  • 10Sun WH,Kreisle RA,Kischer CW,et al.In rive and in vitro characteristics of interleukin-6 transfected B16 melanoma cell [J].Cancer Res,1992,53:5412.

二级参考文献46

  • 1梁杰,李建赤,罗少军,张培华,彭智,李平.增生性瘢痕组织内IL-24基因mRNA的表达及意义[J].广东医学院学报,2007,25(2):123-125. 被引量:5
  • 2[1]Gupta P,Su ZZ,Lebedeva IV,et al.Mda-7/IL-24:Multifunctional cancer-specific apoptosis-inducing cytokine.Pharmacol Ther,2006,111(3):596-628.
  • 3[2]Fisher PB,Gopalkrishnan RV,Chada S,et al.Mda-7/IL-24,a novel cancer selective apoptosis inducing cytokine gene:from the laboratory into the clinic.Cancer Biol Ther,2003,2(4):23-37.
  • 4[4]Luo J,Deng ZL,Luo X,Tang N,et al.A protocol for rapid generation of recombinant adenoviruses using the AdEasy system.Nat Protoc.2007;2(5):1236-1247.
  • 5[6]Zhao L,Dong A,Gu J,et al.The antitumor activity of TRAIL and IL-24 with replicating oncolytic adenovirus in colorectal cancer.Cancer Gene Ther.2006 Nov;13 (11):1011-22.Cancer Gene Ther.2006,13(11):1011-1022.
  • 6[7]Leath CA 3rd,Kataram M,Bhagavatula P,et al.Infectivity enhanced adenoviral-mediated mda-7/IL-24 gene therapy for ovarian carcinoma.Gynecol Oncol.2004,94(2):352-362.
  • 7萨姆布鲁克 黄培堂译.分子克隆实验指南[M].北京:科学出版社,2002,8..
  • 8Peacock EE Jr, Madden JW, Treier WC. Biological basis for the treatment of keloids and hypertroghic scars. South Med J, 1970, 63:7655-7676.
  • 9Wang CM, Hyakusoku H , Asano G. Genetic predispositions to keloid and hypertrophic scar. J Jpn Plast Reconstr Surg, 2001, 21:241-246.
  • 10Bettinger DA, Yager DR, Diegelmann RF, et al. The effect of TGF-beta on keloid fibroblast proliferation and collagen synthesis. Plast Reconstr Surg, 1996,98: 827-833.

共引文献58

同被引文献32

  • 1王春梅,百束比古,张启旭,严笠,中泽南堂.瘢痕疙瘩成纤维细胞的基因组学研究[J].中华整形外科杂志,2005,21(4):299-301. 被引量:28
  • 2林跃辉,王敏.PI3-K-AKT信号转导途径与凋亡的关系[J].国际病理科学与临床杂志,2005,25(4):307-310. 被引量:25
  • 3危少华,吴浩荣,朱晔涵,叶震敏,盛伟华,杨吉成.人IL-24重组蛋白免疫刺激及血管形成抑制作用[J].江苏医药,2007,33(3):273-275. 被引量:4
  • 4李建赤,梁杰,罗少军,张培华,彭智,李平.人白细胞介素24mRNA在瘢痕疙瘩中的表达及意义[J].中国组织工程研究与临床康复,2007,11(32):6432-6435. 被引量:6
  • 5Lebedeva Ⅳ,Emdad L,Su ZZ,et al.mda-7/IL-24,novel anticancer cytokine:focus on bystander antitumor,radiosensitization and antiangio-genic properties and overview of the phase Ⅰ clinical experience[J].Int J Oncol,2007,31:985-1007.
  • 6Mhashilkar AM,Schrock BD,Hindi M,el al.Melanoma differentiation associated gene-7 (mda-7) a novel anti-tumor gone for cancer gene therapy[J].Mol Med,2001,7:271-282.
  • 7Shi H,Wei LL,Yuan CF,et al.Melanoma differentiationassociated gene-7/interleukin 24 inhibits invasion and migration of human cervical cancer cells in vitro[J].Saudi Med J,2007,28:1671-1675.
  • 8Ramesh R,Ito I,Gopalan B,et al.Ectopic production of MDA-7/IL-24 inhibits invasion and migration of human lung cancer cells[J].Mol Ther,2004,9:510-518.
  • 9Wang M,Tan Z,Thomas EK.Conservation of the genomic strocture and receptor-mediated signaling between human and rat IL-24[J].Genes lmmun,2004,5:363-370.
  • 10Zhuo B,Wang R,Zhang H,et al.Interleukin-24 inhibits cell migration and invasion in the neuroblastoma cell line SH-SY5Y[J].Oncology reports,2013,30:2749-2754.

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