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子痫前期胎盘组织中检测到的细胞因子相关基因和氧化相关基因。

Cytokine-related genes and oxidation-related genes detected in preeclamptic placentas.

机构信息

Department of Obstetrics and Gynecology, Catholic University of Korea, Soechoe-dong, Banpo-gu, Seoul, Republic of Korea.

出版信息

Arch Gynecol Obstet. 2010 Oct;282(4):363-9. doi: 10.1007/s00404-009-1222-x. Epub 2009 Sep 29.

Abstract

PURPOSE

To investigate cytokine- and oxidation-related genes for preeclampsia using DNA microarray analysis.

METHODS

Placentas were collected from 13 normal pregnancies and 13 patients with preeclampsia. Gene expression was studied using DNA microarray. Among significantly expressed genes, we focused on genes associated with cytokines and oxidation, and the results were confirmed using quantitative real time-polymerase chain reaction (QRT-PCR).

RESULTS

415 genes out of 30,940 genes were altered by > or =2-fold in the microarray analysis. 121 up-regulated genes and 294 down-regulated genes were found to be in preeclamptic placenta. Six cytokine-related genes and 5 oxidation-related genes were found from among the 121 up-regulated genes. The cytokine-related genes studied included oncostatin M (OSM), fms-related tyrosine kinase (FLT1) and vascular endothelial growth factor A (VEGFA), and the oxidation-related genes studied included spermine oxidase (SMOX), l cytochrome P450, family 26, subfamily A, polypeptide 1 (CYP26A1), acetate dehydrogenase A (LDHA). These six genes were also significantly higher in placentas from patients with preeclampsia than in those from women with normal pregnancies. The placental tissue of patients with preeclampsia showed significantly higher mRNA expression of these six genes than the normal group, using QRT-PCR.

CONCLUSION

DNA microarray analysis is one of the great methods for simultaneously detecting the functionally associated genes of preeclampsia. The cytokine-related genes such as OSM, FLT1 and VEGFA, and the oxidation-related genes such as LDHA, CYP26A1 and SMOX might prove to be the starting point in the elucidation of the pathogenesis of preeclampsia.

摘要

目的

运用 DNA 微阵列分析探讨子痫前期相关细胞因子和氧化基因。

方法

收集 13 例正常妊娠胎盘和 13 例子痫前期患者胎盘,应用 DNA 微阵列进行基因表达谱研究。在差异表达基因中,我们重点关注与细胞因子和氧化相关的基因,并采用实时定量聚合酶链反应(QRT-PCR)对结果进行验证。

结果

在微阵列分析中,有 415 个基因(占 30940 个基因的>或=2 倍)发生改变。在子痫前期胎盘组织中发现 121 个上调基因和 294 个下调基因。在 121 个上调基因中发现 6 个细胞因子相关基因和 5 个氧化相关基因。研究的细胞因子相关基因包括肿瘤坏死因子相关诱导配体(OSM)、fms 相关酪氨酸激酶(FLT1)和血管内皮生长因子 A(VEGFA),氧化相关基因包括精脒氧化酶(SMOX)、细胞色素 P450,家族 26,亚家族 A,多肽 1(CYP26A1)、乙酰脱氢酶 A(LDHA)。这些基因在子痫前期患者胎盘组织中的表达明显高于正常妊娠患者。QRT-PCR 结果显示,子痫前期患者胎盘组织中这些基因的 mRNA 表达明显高于正常组。

结论

DNA 微阵列分析是同时检测子痫前期相关功能基因的一种很好的方法。OSM、FLT1 和 VEGFA 等细胞因子相关基因以及 LDHA、CYP26A1 和 SMOX 等氧化相关基因可能成为阐明子痫前期发病机制的起点。

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