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肿瘤转移抑制因子TXNIP基因与精神分裂症易感性研究

The study of susceptibility to metastasis suppressor TXNIP gene in schizophrenia.
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摘要 目的研究肿瘤转移抑制因子TXNIP在精神分裂症患者和正常对照外周血白细胞中的表达水平,分析该基因与疾病的关系。方法采用TaqMan MGB探针法的绝对定量PCR分析30例首发未服用抗精神病药物、30例复发服用抗精神病药物治疗的精神分裂症患者及30名正常对照TXNIP基因的表达水平。采用阳性和阴性症状量表(PANSS)评定患者病情并由此将患者组分为不同亚组,比较各患者组和对照组间TXNIP基因表达的差异。结果①总患者组TXNIP基因的平均表达水平比对照组低30.2%(P=0.03),而复发服药患者组比对照组低94.0%(P<0.01),首发未服药组比对照组高33.6%(P<0.01)。②未发现各患者组TXNIP基因表达量与PANSS评分、服药剂量相关。③复发服药患者中有家族史的患者TXNIP基因的表达量低于无家族史患者(P=0.01)。结论提示TXNIP基因可能是精神分裂症新的候选基因,抗精神病药物可能降低TXNIP基因的表达。 Objective To investigate the expression of TXNIP gene in peripheral leucocytes from patients with schizophrenia. Methods We measured expression levels of TXNIP in the leukocytes from 30 recurrent patients taking antipsychotic medicine, 30 first-episode drug-nai've patients, and 30 healthy controls using absolute TaqMan real-time quantitative PCR. Further, the two ease groups were divided into different subgroups using Positive and Negative Syndrome Scale (PANSS) respectively and then assessed the expression of TXNIP gene among different subgroups. Results ① The average expression level of TXNIP in leucocytes from total patients with schizophrenia was significantly lower than that of healthy controls by 30. 2% ( P = 0. 03 ). That of the recurrent taking antipsychotie medicine group was much lower than that of healthy control group by 94. 0% ( P 〈 0. 01 ), while that of the first-episode drug-naive group was higher than that of healthy control group by 33.6% ( P 〈 0.01 ) ; ②There was no significant correlation between the expression of TXNIP and the scores of PANSS and the dose of antipsychotic medicines. ③ The average expression of TXNIP in patients with family history of schizophrenia was significant lower than that of without family history (P = 0. 01 ). Conclusions The results suggest that TXNIP might be a novel candidate gene conferring susceptibility to schizophrenia and antipsychotie medicines might decrease the expression of TXNIP gene.
出处 《中国神经精神疾病杂志》 CAS CSCD 北大核心 2008年第9期529-532,共4页 Chinese Journal of Nervous and Mental Diseases
基金 国家自然科学基金项目(编号:30670755) 上海市精神疾病临床医学中心科研基金【编号:K-04(1)】
关键词 精神分裂症 TXNIP 基因表达 TaqMan实时定量PCR Schizophrenia TXNIP Gene expression TaqMan Real-Time PCR
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  • 1崔东红,姚华,王新源,朱滨,江开达.精神分裂症患者外周血白细胞基因差异表达的基因芯片研究[J].中华精神科杂志,2004,37(1):4-8. 被引量:9
  • 2Hakak Y, Walker JR, Li C, et al. Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia[J]. Proc Nail Acad Sci USA, 2001,98(8) : 4746 -4751.
  • 3Brzustowicz LM, Hodgkinson KA, Chow EW, et al. Location of a major susceptibility locus for familial schizophrenia on chromosome lq21 -q22[J]. Science, 2000, 288(5466): 678-682.
  • 4蔡贵庆,伍新尧,李涛,David A.Collier,刘协和,冯炳建,邓红,童大跃,李建金,区敬华.中国人群中家族性精神分裂症与1号染色体的连锁分析[J].中华医学遗传学杂志,2002,19(6):491-494. 被引量:8
  • 5Takagi Y, Tokime T, Nozaki K, et al. Redox control of neuronal damage during brain isehemia after middle cerebral artery occlusion in the rat: imrnunohistochemical and hybridization studies of thioredoxin[J]. J Cereb Blood Flow Metab, 1998, 18(2) : 206 - 214.
  • 6Song H, Cho D, Jeon JH, et al. Vitamin D(3) up-regulating protein 1 ( VDUP1 ) antisense DNA regulates tumorigenicity and melanogenesis of murine melanoma cells via regulating the expression of fas ligand and reactive oxygen species [ J ]. Immunol Lett, 2003, 86(3) : 235 -247.
  • 7Cohen M, Dembling B, Schoding J. The association between schizophrenia and cancer: a population-based mortality study[ J ]. Schizophr Res,2002, 57 (2 - 3 ) : 139 - 146.
  • 8Catts and Catts Apoptosis and schizophrenia: is the tumour suppressor gene, p53, a candidate susceptibility gene? [J]. Schizophr Res, 2000,41 (3) :405 -415.
  • 9Cui DH, Jiang KD, Jiang SD, Xu YF, Yao H. The tumor suppressor adenomatous polyposis coli gene is associated with susceptibility to schizophrenia[ J ]. Mol Psychiatry, 2005, 10 ( 7 ) : 669 - 677.
  • 10于剑锋,彭裕文,崔东红.APC基因与精神分裂症及其他相关神经精神疾病[J].中国神经精神疾病杂志,2008,34(6):383-384. 被引量:5

二级参考文献42

  • 1张向阳,周东丰.精神分裂症的免疫学研究进展[J].国外医学(精神病学分册),1995,22(2):74-79. 被引量:36
  • 2蔡文琴 李海标.发育神经生物学[M].北京:科学出版社,2001.76-97,142-174.
  • 3Herrera L, Kakati S, Gibas L, et al. Gardner syndrome in a man with an interstitial deletion of 5q [J]. Am J Med Genet, 1986, 25 (3) :473 -476.
  • 4Hockey KA, Mulcahy MT, Montgomery P, et al. Deletion of chromosome 5q and familial adenomatous polyposis [J]. J Med Genet, 1989, 26(1) : 61 -62.
  • 5Kinzler KW, Nilbert MC, Su LK, et al. Identification of FAP locus genes from chromosome 5q21 [J]. Science, 1991, 253 (5020) : 661 -665.
  • 6Groden J, Thliveris A, Samowitz W, et al. Identification and characterization of the familial adenomatous polyposis coli gene [J]. Cell, 1991, 66(3) : 589 -600.
  • 7Chealde JP, Krawczak M, Thomas MW, et al. Different combination of biallelic APC mutation confer different growth advantages in colorectal tumours [J]. Cancer Res, 2002, 62(2): 363 -366.
  • 8Senda T, Shimomura A, lizuka-Kogo A. Adenomatous polyposis coli (Apc) tumor suppressor gene as a muhifunctional gene [J]. Anat Sci Int, 2005, 80 (3) : 121 - 131.
  • 9Kawasaki Y, Senda T, ]shidate T, et al. Asef, a link between the tumor suppressor APC and G-protein signaling [ J ]. Science, 2000, 289(5482) : 1194 - 1197.
  • 10Senda T, Iino S, Matsushita K, et al. Localization of the adenomatous polyposis coli tumour suppressor protein in the mouse central nervous system [J]. Neuroscience, 1998, 83(3) : 857 -866.

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