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颅咽管瘤中RARα及PPARβ/δ表达与RA作用的相关性

Correlation between the Expression of RARα, PPARβ/δ and the Effect of Retinoic Acid in Craniopharyngioma Cells
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摘要 目的检测颅咽管瘤中RARα及PPARβ/δ的表达,分析其表达量与RA作用效果的相关性,探讨RA靶向治疗颅咽管瘤的分子机制.方法 RT-PCR法检测31例体外培养的颅咽管瘤细胞中PPARβ/δ、RARα的表达情况,MTT法测定RA对PPARβ/δ、RARα不同表达的颅咽管瘤细胞的抑制率,分析其表达情况与RA作用是否存在相关性.结果 (1)RT-PCR结果显示,不同颅咽管瘤细胞中PPARβ/δ、RARα表达存在差别.31例原代培养的颅咽管瘤细胞按其核受体表达不同分为PPARβ/δ>RARα、RARα>PPARβ/δ、RARα>>PPARβ/δ3组;(2)MTT结果显示在相同RA药物作用下RARα>>PPARβ/δ组的抑制率明显高于RARα>PPARβ/δ组、PPARβ/δ>RARα和对照组,差异有统计学意义(P<0.05).结论 (1)PPARβ/δ、RARα的表达可作为评估RA治疗颅咽管瘤效果的有效指标.PPARβ/δ表达低的颅咽管瘤细胞对RA更敏感;(2)靶向升高RARα或者靶向降低PPARβ/δ的表达都有益于颅咽管瘤的治疗. Objective To investigate the molecular mechanism of retinoic acid in targeted treatment of craniopharyngioma by detecting the expression of RARαand PPARβ/δin craniopharyngioma cells and analyzing the correlation between the expression and effect of retinoic acid. Methods The expression of RARα and PPARβ/δ in craniopharyngioma cells from 31 patients cultured in vitro was quantified by reverse transcription-PCR. The inhibition rates of RA on craniopharyngioma with different expression of RARα and PPARβ/δ were detected by using MTT assay, and the correlation between the expression of RARα and PPARβ/δand the effect of RA was analyzed. Results 1. The RT-PCR results showed that the expression levels of PPARβ/δand RARα mRNA were different. Craniopharyngioma cells from 31 patients in primary culture were divided into three groups according the expression levels of nuclear receptor: PPARβ/δ〉RARα group, RARα〉PPARβ/δ group and RARα〉〉PPARβ/δ group. 2.MTT results showed that the inhibition rate of RARα〉〉PPARβ/δgroup was significantly higher than the other groups under same drug, the differences had statistical significance ( 〈0.01) . Conclusions The expression of PPARβ/δ, RARα can be used to evaluate the effect of RA in treatment of craniopharyngioma. The craniopharyngioma with low-expression of PPARβ/δ is more sensitive to RA. Targeting higher RARα or targeting lower PPARβ/δ is beneficial to the treatment of craniopharyngiomas.
出处 《昆明医科大学学报》 CAS 2013年第10期42-46,共5页 Journal of Kunming Medical University
基金 云南省科技厅专项研究基金资助项目(2008CD038)
关键词 过氧化物酶体增殖物活化受体 β δ核维甲酸受体 颅咽管瘤 Peroxisome Proliferators Activated Receptor β/δ Retinoid acid receptor Craniol)haryngioma
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  • 1Bin WU Jie GAO Ming-wei WANG~2 The National Center for Drug Screening,Shanghai Institute of Materia Medica,Shanghai Institutes for Biological Sciences,Chinese Academy of Sciences,Graduate School of Chinese Academy of Sciences,Shanghai 201203,China.Development of a complex scintillation proximity assay for highthroughput screening of PPAR7 modulators[J].Acta Pharmacologica Sinica,2005,26(3):339-344. 被引量:12
  • 2Mangelsdorf DJ, Thummel C, Beato M, Herrlich P, Schutz G,Umesono K, et al. The nuclear receptor superfamily: the second decade. Cell 1995; 83: 835-9.
  • 3Schmidt A, Endo N, Rutledge S J, Vogel R, Shinar D, Rodan GA.Identification of a new member of the steroid hormone receptor superfamily that is activated by a peroxisome proliferators and fatty acids. Mol Endocrinol 1992; 6: 1634-41.
  • 4Sher T, Yi HE McBride OW, Gonzalez FJ. cDNA cloning, chromosomal mapping and functional characterization of the human peroxisome proliferator activated receptor. Biochemistry 1993; 32: 5598-604.
  • 5Desvergne B, Wahli W. Peroxisome proliferator-activated receptors:nuclear control of metabolism. Endocr Rev 1999; 20: 649-88.
  • 6Wise H. Multiple signalling options for prostacyclin. Acta Pharmacol Sin 2003; 24: 625-30.
  • 7Kliewer SA, Umesono K, Noonan DJ, Heyman RA, Evans RM. Convergence of 9-cis retinoic acid and peroxisome proliferator signalling pathways through heterodimer formation of their receptors. Nature 1992; 358: 771-4.
  • 8Ijpenberg A, Jeannin E, Wahli W, Desvergne B. Polarity and specific sequence requirements of PPAR-RXR heterodimer binding to DNA:a functional analysis of the malic enzyme gene PPRE. J Biol Chem.1997;272: 20108-17.
  • 9Juge-Aubry C, Pernin A, Favez T, Burger AG, Wahli W, Meier CA, et al. DNA binding properties of peroxisome proliferator-activated receptor subtypes on various natural peroxisome proliferator response elements: importance of the 5' flanking region. J Biol Chem 1997;272: 25252-9.
  • 10Yu K, Bayona W, Kallen CB, Harding HE Ravera CP, McMahon G,et al. Differential activation of peroxisome proliferator-activated receptors by eicosanoids. J Biol Chem 1995; 270: 23975-83.

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