Department of Psychology, McGill University, Montreal, QC, Canada H3A 1B1 Department of Anesthesia Research, Faculty of Dentistry, McGill University, Montreal, QC, Canada H3A 1B1 Alan Edwards Centre for Research on Pain, McGill University, Montreal, QC, Canada H3A 1B1.
Pain. 2011 Aug;152(8):1888-1898. doi: 10.1016/j.pain.2011.04.014. Epub 2011 May 10.
Existing microarray gene expression profiling studies of tonic/chronic pain were subjected to meta-analysis to identify genes found to be regulated by these pain states in multiple, independent experiments. Twenty studies published from 2002 to 2008 were identified, describing the statistically significant regulation of 2254 genes. Of those, a total of 79 genes were found to be statistically significant "hits" in 4 or more independent microarray experiments, corresponding to a conservative P<0.01 overall. Gene ontology-based functional annotation clustering analyses revealed strong evidence for regulation of immune-related genes in pain states. A multi-gene quantitative real-time polymerase chain reaction experiment was run on dorsal root ganglion (DRG) and spinal cord tissue from rats and mice given nerve (sciatic chronic constriction; CCI) or inflammatory (complete Freund's adjuvant) injury. We independently confirmed the regulation of 43 of these genes in the rat-CCI-DRG condition; the genetic correlates in all other conditions were largely and, in some cases, strikingly, independent. However, a handful of genes were identified whose regulation bridged etiology, anatomical locus, and/or species. Most notable among these were Reg3b (regenerating islet-derived 3 beta; pancreatitis-associated protein) and Ccl2 (chemokine [C-C motif] ligand 2), which were significantly upregulated in every condition in the rat.
现有的关于强直性/慢性疼痛的基因表达微阵列研究进行了荟萃分析,以确定在多个独立实验中受这些疼痛状态调节的基因。从 2002 年到 2008 年共确定了 20 项研究,描述了 2254 个基因的统计学上显著调节。其中,在 4 个或更多独立的微阵列实验中,共有 79 个基因被发现具有统计学意义的“命中”,对应于总体上保守的 P<0.01。基于基因本体论的功能注释聚类分析表明,在疼痛状态下存在对免疫相关基因的强烈调节证据。对接受神经(坐骨慢性缩窄;CCI)或炎症(完全弗氏佐剂)损伤的大鼠和小鼠的背根神经节(DRG)和脊髓组织进行了多基因实时聚合酶链反应实验。我们独立证实了在大鼠 CCI-DRG 条件下 43 个这些基因的调节;在所有其他条件下的遗传相关性在很大程度上,并且在某些情况下,非常显著,是独立的。然而,确定了一些基因的调节跨越了病因、解剖部位和/或物种。其中最值得注意的是 Reg3b(再生胰岛衍生 3β;胰腺炎相关蛋白)和 Ccl2(趋化因子 [C-C 基序] 配体 2),它们在大鼠的所有条件下均显著上调。