Bukowski Radek, Hankins Gary D V, Saade George R, Anderson Garland D, Thornton Steven
Department of Obstetrics and Gynecology, University of Texas Medical Branch at Galveston, Galveston, Texas, USA.
PLoS Med. 2006 Jun;3(6):e169. doi: 10.1371/journal.pmed.0030169. Epub 2006 Jun 13.
Preterm labor, failure to progress, and postpartum hemorrhage are the common causes of maternal and neonatal mortality or morbidity. All result from defects in the complex mechanisms controlling labor, which coordinate changes in the uterine fundus, lower segment, and cervix. We aimed to assess labor-associated gene expression profiles in these functionally distinct areas of the human uterus by using microarrays.
Samples of uterine fundus, lower segment, and cervix were obtained from patients at term (mean +/- SD = 39.1 +/- 0.5 wk) prior to the onset of labor (n = 6), or in active phase of labor with spontaneous onset (n = 7). Expression of 12,626 genes was evaluated using microarrays (Human Genome U95A; Affymetrix) and compared between labor and non-labor samples. Genes with the largest labor-associated change and the lowest variability in expression are likely to be fundamental for parturition, so gene expression was ranked accordingly. From 500 genes with the highest rank we identified genes with similar expression profiles using two independent clustering techniques. Sets of genes with a probability of chance grouping by both techniques less than 0.01 represented 71.2%, 81.8%, and 79.8% of the 500 genes in the fundus, lower segment, and cervix, respectively. We identified 14, 14, and 12 those sets of genes in the fundus, lower segment, and cervix, respectively. This enabled networks of co-regulated and co-expressed genes to be discovered. Many genes within the same cluster shared similar functions or had functions pertinent to the process of labor.
Our results provide support for many of the established processes of parturition and also describe novel-to-labor genes not previously associated with this process. The elucidation of these mechanisms likely to be fundamental for controlling labor is an important prerequisite to the development of effective treatments for major obstetric problems--including prematurity, with its long-term consequences to the health of mother and offspring.
早产、产程停滞和产后出血是孕产妇和新生儿死亡或发病的常见原因。这些均源于控制分娩的复杂机制存在缺陷,该机制协调子宫底、子宫下段和宫颈的变化。我们旨在通过使用微阵列评估人类子宫这些功能不同区域中与分娩相关的基因表达谱。
在分娩开始前(n = 6)或自然发动分娩的活跃期(n = 7),从足月(平均±标准差 = 39.1±0.5周)患者获取子宫底、子宫下段和宫颈样本。使用微阵列(人类基因组U95A;Affymetrix)评估12,626个基因的表达,并在分娩样本和未分娩样本之间进行比较。与分娩相关变化最大且表达变异性最低的基因可能是分娩的基础,因此对基因表达进行了相应排名。从排名最高的500个基因中,我们使用两种独立的聚类技术鉴定出具有相似表达谱的基因。两种技术随机分组概率均小于0.01的基因集分别占子宫底、子宫下段和宫颈中500个基因的71.2%、81.8%和79.8%。我们分别在子宫底、子宫下段和宫颈中鉴定出14、14和12个这样的基因集。这使得能够发现共同调控和共同表达的基因网络。同一簇内的许多基因具有相似功能或与分娩过程相关的功能。
我们的结果为许多已确立的分娩过程提供了支持,还描述了以前与该过程无关的与分娩相关的新基因。阐明这些可能是控制分娩基础的机制是开发针对主要产科问题(包括早产及其对母婴健康的长期影响)的有效治疗方法的重要前提。