DNA microarray data integration by ortholog gene analysis reveals potential molecular mechanisms of estrogen-dependent growth of human uterine fibroids
© Wei et al; licensee BioMed Central Ltd. 2007
Received: 07 November 2006
Accepted: 02 April 2007
Published: 02 April 2007
Uterine fibroids or leiomyoma are a common benign smooth muscle tumor. The tumor growth is well known to be estrogen-dependent. However, the molecular mechanisms of its estrogen-dependency is not well understood.
Differentially expressed genes in human uterine fibroids were either retrieved from published papers or from our own statistical analysis of downloaded array data. Probes for the same genes on different Affymetrix chips were mapped based on probe comparison information provided by Affymetrix. Genes identified by two or three array studies were submitted for ortholog analysis. Human and rat ortholog genes were identified by using ortholog gene databases, HomoloGene and TOGA and were confirmed by synteny analysis with MultiContigView tool in the Ensembl genome browser.
By integrated analysis of three recently published DNA microarray studies with human tissue, thirty-eight genes were found to be differentially expressed in the same direction in fibroid compared to adjacent uterine myometrium by at least two research groups. Among these genes, twelve with rat orthologs were identified as estrogen-regulated from our array study investigating uterine expression in ovariectomized rats treated with estrogen. Functional and pathway analyses of the twelve genes suggested multiple molecular mechanisms for estrogen-dependent cell survival and tumor growth. Firstly, estrogen increased expression of the anti-apoptotic PCP4 gene and suppressed the expression of growth inhibitory receptors PTGER3 and TGFBR2. Secondly, estrogen may antagonize PPARγ signaling, thought to inhibit fibroid growth and survival, at two points in the PPAR pathway: 1) through increased ANXA1 gene expression which can inhibit phospholipase A2 activity and in turn decrease arachidonic acid synthesis, and 2) by decreasing L-PGDS expression which would reduce synthesis of PGJ2, an endogenous ligand for PPARγ. Lastly, estrogen affects retinoic acid (RA) synthesis and mobilization by regulating expression of CRABP2 and ALDH1A1. RA has been shown to play a significant role in the development of uterine fibroids in an animal model.
Integrated analysis of multiple array datasets revealed twelve human and rat ortholog genes that were differentially expressed in human uterine fibroids and transcriptionally responsive to estrogen in the rat uterus. Functional and pathway analysis of these genes suggest multiple potential molecular mechanisms for the poorly understood estrogen-dependent growth of uterine fibroids. Fully understanding the exact molecular interactions among these gene products requires further study to validate their roles in uterine fibroids. This work provides new avenues of study which could influence the future direction of therapeutic intervention for the disease.
Leiomyoma or uterine fibroids are the most common benign tumor, occurring in approximately 60% of women during their lifetime. In spite of its generally benign nature, uterine fibroids cause an array of substantial health problems in some women such as pressure or pain, excessive uterine bleeding and problems related to pregnancy . As a consequence, uterine fibroids account for approximately one-third of all hysterectomies in the United States or about 200,000 hysterectomies per year 
Although the etiology of the disease is largely unknown, it is clear that growth of uterine fibroids depends on the ovarian hormones estrogen and progesterone . This hormonal dependency is supported by the following observations. Uterine fibroids are observed only after menarche, increase in size during pregnancy, and frequently regress after menopause (reviewed in ). The tumors can be induced to regress by surgical ovariectomy or by treatment with GnRH agonists which induce a hypoestrogenic state. Tissue estrogen concentrations are elevated in uterine fibroids compared to myometrium, which may result from increased aromatase activity . Estrogen produces diverse biological effects mediated by estrogen receptors (ER). When bound to estrogen, the ER modulates the transcriptional activity of target genes [6, 7]. Evidence shows that one effect of estrogen is to increase the levels of both estrogen receptor (ER) and progesterone receptor (PR) . It has been recently demonstrated that estrogen can stabilize ER mRNA, increasing the level of cellular ER protein .
While it is well established that growth of uterine fibroids depends on estrogen, molecular mechanisms of such estrogen dependency are largely unknown. Numerous studies have indicated that estrogen may mediate fibroid growth through the mitogenic effects of growth factors such as transforming growth factor-β and basic fibroblast growth factor (reviewed in ). There have been a few recent studies addressing molecular mechanisms of functional interaction between estrogen signaling and growth factor-mediated signaling in the pathogenesis of uterine fibroids. Work by Hayashi et al  in estrogen-dependent cancers provides an example where the constitutively activated MAPK signaling pathway in endometrial cancer cells might enhance the transcriptional activity of ERα via phosphorylation of its AF-1 domain. Wnt signaling was recently implicated in the pathogenesis of uterine fibroids where the secreted frizzled related protein 1 (sFRP1) mRNA  was found to be significantly elevated in the tumor, and regulated by estrogen treatment. It was shown that sFRP1 contributes to fibroid growth through an anti-apoptotic effect.
A recent report has shown that PPARγ activation by its ligand (i.e., prostaglandin J2) in uterine fibroids is growth inhibitory and mediated at least in part by negative cross-talk between ER and PPARγ signaling pathways . However, the exact molecular mechanisms of how such interaction occurs between the two nuclear receptor signaling pathways remain to be answered. Elevated levels of PPARγ, retinoid × receptor alpha (RXRα), and all-trans retinoic acid were observed in human uterine fibroids, and retinoids in combination with estrogen was shown to induce development of uterine fibroids in a guinea pig model .
DNA microarray technology allows simultaneous interrogation of tens of thousands of genes . Several studies have applied the technology to identify genes that were differentially expressed in human uterine fibroids compared to adjacent normal myometrium . The technology has also been applied to identify estrogen-regulated genes in the adult rat uterus . To understand the molecular interactions involved in estrogenic support of uterine fibroid growth, we integrated results from the above DNA microarray studies using ortholog analysis. Orthologous genes are related by direct evolutionary descent and should play similar developmental or physiological roles . This study identified twelve human and rat orthologous genes that were differentially expressed in human uterine fibroids and estrogen-regulated in the adult rat uterus, and describes their possible cellular and physiological roles in estrogen-dependent tumor growth.
Published DNA microarray data sets
Published DNA microarray experiments
No of Genes Identified
Uterine fibroids and normal myometrium
Uteri from vehicle and estrogen treated animals
5 rats per treatment, 2 chip for each animal
Identification of human and rat ortholog genes that are estrogen responsive and differentially expressed in uterine fibroids
To calculate functional distribution of the human genes differentially expressed in uterine fibroids, a web tool FatiGO developed by  was used according to its on-line instruction.
Genes differentially expressed in human uterine fibroids
Genes with differential expression in human uterine fibroids identified by two or three groups of researchers.
ATP-binding cassette, sub-family A (ABC1), member 8
actin binding LIM protein 1
aldehyde dehydrogenase 1 family, member A1
activating transcription factor 3
complement component 1, s subcomponent
chromosome 5 open reading frame 13
carbonic anhydrase XII
calcitonin receptor-like receptor
carboxypeptidase A3 (mast cell)
cellular retinoic acid binding protein 2
cysteine-rich, angiogenic inducer, 61
EGF-containing fibulin-like extracellular matrix protein 1
v-fos FBJ murine osteosarcoma viral oncogene homolog
G antigen, family C, 1
glutamate receptor, ionotropic, AMPA 2
insulin-like growth factor 2 (somatomedin A)
insulin-like growth factor binding protein 6
kinesin family member 5C
v-maf musculoaponeurotic fibrosarcoma oncogene homolog F (avian)
mitogen-activated protein kinase kinase kinase 5
mesoderm specific transcript homolog (mouse)
nuclear receptor subfamily 4, group A, member 1
Purkinje cell protein 4
phosphoinositide-3-kinase, regulatory subunit, polypeptide 1 (p85 alpha)
proteolipid protein 1 (Pelizaeus-Merzbacher disease, spastic paraplegia 2, uncomplicated)
prostaglandin D2 synthase 21kDa (brain)
prostaglandin E receptor 3 (subtype EP3)
ribonuclease, RNase A family, 4
serine (or cysteine) proteinase inhibitor, clade E, member 1
SRY (sex determining region Y)-box 4
transforming growth factor, beta receptor II
thymosin, beta, identified in neuroblastoma cells
tryptase beta 2
Estrogen-regulated genes in the uterus of ovariectomized adult rats
Helvering et al  evaluated short and long-term effects of ovariectomy and treatment with estrogen on expression changes in the uterus of ovariectomized rats. They found that ovariectomy induced dramatic gene expression changes in the uterus both at 13 days and at 5 weeks post surgery with 1930 or 2908 Affymetrix probes changed, respectively. Treatment of ovariectomized rats with 0.1 mg/kg/day 17-β ethinyl estradiol also induced significant changes with 2389 probes altered following 1-day of treatment and 2990 probes following 5-week treatment. In total, there were 3927 Affymetrix probe sets that were changed by ovariectomy and then altered in the opposite direction by estrogen treatment of ovariectomized rats at two time points.
Identification of orthologous genes differentially expressed in human uterine fibroids and regulated by estrogen in the rat uterus
Human and rat orthologous genes differentially expressed in human uterine fibroids and E2-responsive in the rat uterus.
Previous reports on E2 regulation
prostaglandin E receptor 3 (subtype EP3)
transforming growth factor, beta receptor II (70/80kDa)
Purkinje cell protein 4
calcitonin receptor-like receptor
aldehyde dehydrogenase 1 family, member A1
cellular retinoic acid binding protein 2
prostaglandin D2 synthase 21kDa (brain)
[30, 31] 
nuclear receptor subfamily 4, group A, member 1
proteolipid protein 1
ribonuclease, RNase A family, 4
insulin-like growth factor 2 (somatomedin A)
Contradictory to   
To confirm that the Affymetrix probe sets were indeed specific for each gene we confirmed their alignment with the human and rat genomes using the BLAT tool  at UCSC . Except for Affymetrix target sequence of rat gene C1S which produced two major alignments in the q42 cytoband of rat chromosome 4, one spanning 160981068 to 160993069 with 98.6% identities and the other spanning 160609849 to 160612122 with 75.7% identities, Affymetrix target sequences of all the other twelve genes generated one major alignment to the expected gene in the human and rat genomes. For example, the rat target sequence for the rat L-PGDS gene had a single, major alignment with the L-PGDS gene on chromosome 3 in the rat genome and the human target sequence generated a single alignment with L-PGDS gene on chromosome 9 in the human genome. Thus we believe that expression signals of the twelve human and rat orthologs, except for the gene C1S, obtained by Affymetrix chips used in these studies could accurately measure mRNA abundance of the twelve genes in the human and rat samples.
A literature search was conducted for each of the twelve genes to determine if others have previously identified these genes to be directly regulated by estrogen (Table 3). Cellular retinoic acid binding protein 2 (CRABP2) and aldehyde dehydrogenase 1 A1 (ALDH1A1) were previously shown to directly respond to estrogen in the rat uterus [28, 29] in the same fashion as observed by Helvering using DNA microarray. Lipocalin-type prostaglandin D synthase (L-PGDS) was reported to respond to estrogen in a more complicated fashion depending on the tissues/organs. For example, L-PGDS transcription was induced in the medial basal hypothalamus and repressed in the preoptic area in female adult mice by estrogen [30, 31]. Transcription of L-PGDS was also induced in mouse heart in vivo specifically by estrogen receptor beta via a functional estrogen-responsive element in the L-PGDS promoter . Castro-Caldas et al  demonstrated that estrogen induced de novo expression of annexin A1 (ANXA1) and stimulated its secretion in the human CCRF-CEM acute lymphoblastic leukemia cell line apparently via a mechanism independent of the intracellular estrogen receptor. Consistent with this result we couldn't find any putative estrogen responsive element in its 5 kb promoter sequence. Expression of calcitonin receptor-like receptor (CALCRL) was inhibited by estrogen in the rat uterus  and placenta . Nuclear receptor subfamily 4, group A, member 1 (NR4A1) whose human promoter harbors a potential estrogen-responsive element (ERE) , was reported  to be an early responsive gene in the ovarectomized rat uterus to estrogen treatment. Insulin-like growth factor II (IGF2) was regulated in the estrogen-treated rat uterus (Table 3), but had previously been reported to be estrogen non-responsive. Rather, IGF-1 was found to be regulated by estrogen in human uterine fibroids , rhesus monkey myometrium  and rat uterus .
In summary, by integrating multiple independent DNA microarray studies of differentially expressed genes in human uterine fibroids a group of thirty-eight genes were identified as consistently changed in the tumor versus surrounding normal myometrium. By ortholog gene analysis we identified a subset of these genes that were estrogen-regulated in the rat array study. Six of the twelve ortholog genes have previously been described to be regulated by estrogen while the remaining genes have yet to be independently verified as estrogen-responsive.
DNA microarray technology provides us with a great opportunity for looking at molecular mechanisms of disease development on a whole genome scale. While a few public databases have been built to facilitate data sharing [20, 41, 42], it still remains a great challenge to integrate the data, particularly data generated from different organisms, in order to generate testable hypotheses. In the present work we integrated multiple microarray data sets generated by independent research groups from two different species using ortholog gene analysis to try to discover molecular clues to estrogen-dependent growth of human uterine fibroids. While this in silico analysis suggests pathways and individual gene product involvement in the regulation of fibroid tumor growth by estrogenic signaling, the authors recognize the need for experimental follow-up to prove these associations.
Thirty-eight human genes (Table 2) were identified in common from three independent studies showing differential expression between uterine fibroids and normal myometrium. Of these, twelve human and rat orthologous genes (Table 3) were shown to be estrogen-regulated in the rat uterus. Since they are human and rat orthologs, we inferred that they should share similar expression regulation and biological functions in both species. These genes provide important clues to understand estrogen-dependent growth of human uterine fibroids.
Prostaglandin E2 receptor subtype 3 (PTGER3 or EP3) is a G-protein-coupled receptor activated by prostaglandin E2 that was down regulated in uterine fibroids. Alternative splicing generates three isoforms: EP3 alpha, EP3 beta and EP3 gamma, which differ in the putative cytoplasmic carboxy-terminal tail. It was demonstrated that while EP3 gamma is coupled to both stimulation and inhibition of adenylate cyclase, EP3 alpha and beta are exclusively coupled to inhibition of adenylate cyclase . Shoji et al.  demonstrated that EP3 plays an important role in suppression of cell growth and its down-regulation enhances colon carcinogenesis at a later stage. Transforming growth factor-beta (TGF-β) is a potent inhibitor of normal epithelial cell proliferation and is increasingly implicated in fibroid growth. Many tumor cell lines do not respond to the inhibitory effects of TGF-β due to a reduction or absence of the type II receptor (TGF-β R2) . The down-regulation of TGF-β R2 in uterine fibroids is consistent with this finding. The PCP4 gene encoding PEP-19 is a calmodulin-regulatory protein found abundantly within neurons that was found to be increased in uterine fibroids. A study in PC12 cells  demonstrated that PEP-19 could inhibit apoptosis in the cells, suggesting that its up-regulation in human uterine fibroids may be similar. Thus, estrogen may promote cell survival and tumor growth by increasing expression of the anti-apoptotic PCP4 gene and by suppressing the expression of growth inhibitory receptors PTGER3 and TGF-β R2.
The calcitonin receptor-like receptor (CALCRL or CRLR), a G-protein coupled receptor, acts as a receptor for adrenomedullin (ADM) or calcitonin gene related peptide (CGRP) depending on which receptor activity modifying protein (RAMP) it partners with . Using a rat uterine fibroid-derived cell line (ELT3), Thota and Yallampalli  demonstrated that expression of CALCRL and RAMP1 increased with progesterone and decreased with estrogen, consistent with what Helvering et al found in the array work (Table 3). Down-regulation of CALCRL expression in the tumor and in response to estrogen may implicate two important aspects of the tumor growth, that is, cell proliferation and angiogenesis.
L-PGDS has dual molecular functions. It catalyzes the conversion of prostaglandin H2 (PGH2) to prostaglandin D2 (PGD2) inside the cell and binds to small non-substrate lipophilic molecules including retinal, retinoic acid and thyroid hormone and serve as a transporter for these molecules once secreted . ANXA1 is a calcium-dependent phospholipid binding protein and belongs to the annexin family. It was originally identified as a protein that apparently modulated the release of arachidonic acid from cells . Recent data have shown that ANXA1 may specifically target cytosolic phospholipase A2 (PLA2) by both direct enzyme inhibition and suppression of cytokine-induced activation of the enzyme . CRABP2 is a member of a large family of small proteins that specifically bind lipophilic compounds such as fatty acids and retinoids . Recent work has suggested that CRABP2 may have a role in the movement of retinoic acid (RA) to the RA receptors (RARs), thereby enhancing the action of RA in the cells in which it is expressed. ALDH1A1 belongs to the aldehyde dehydrogenase family and is a terminal enzyme of the pathway catalyzing conversion of retinal to RA . NR4A1 (encoded by Nur77 in mouse, NGFI-B in rat, and TR3 in human) is an immediate-early responsive orphan nuclear receptor whose expression is rapidly induced by a variety of extracellular stimuli including estrogen as evidenced here (Table 3). Using Northern blot RNA analysis Cicatiello et al  reported that NR4A1 was transiently activated in the uterus (up to 20-fold) within 30–120 min after treatment of adult ovariectomized rats with estrogen.
Retinoic acid (RA) has been established as a biologically active form of vitamin A (retinol). Fig 4 shows that biosynthesis of RA occurs by two sequential irreversible oxidations, first producing retinal from retinol by retinal dehydrogenases (RolDHs). The retinal is then oxidized to RA by retinal dehydrogenases (RalDHs) of the alcohol dehydrogenase (ADH) family 1 (also known as ALDH1A1-3). Tsibris et al  demonstrated that estrogen induced formation of abdominal fibroids in the guinea pig, and RA in combination with estrogen was required to specifically induce formation of fibroids in the uterus. Estrogen-induced guinea pig uterine fibroids are similar to the human fibroids, in that they also expressed increased levels of PPARγ, RXR-α and all-trans retinoic acid. Our integrated analysis of expression data collected by independent studies revealed that expression of two genes, ALDH1A1 and CRABP2 for RA synthesis or mobilization was differentially expressed in human uterine fibroids and regulated by estrogen in the rat uterus. Previous studies in rodents have suggested that estrogen directly induces uterine RA synthesis by increasing expression of epithelial retinal dehydrogenase (eRolDH) and ALDH1A2 (reviewed in ). Reduction of ALDH1A1 expression (Table 3) may not directly result from estrogen regulation but rather be due to feedback inhibition by RA . RA acts on tumor growth by binding and regulating the tumor cell heterodimeric receptors RAR and RXR. RXR may also exert its effects on tumor cell survival and growth by partnering with PPARγ and/or NR4A1. NR4A1 was originally recognized for its role in cell proliferation and differentiation. It may confer its growth effects by trans-activating target genes required for cell proliferation in nucleus . On the other hand, it also acts on mitochondria (non-trans-activation activity) to induce apoptosis. It was demonstrated that its nuclear export and initiation of NR4A1-dependent apoptosis depends on the nuclear exporting signal (NES) residing on its binding partner RXR and is suppressed by RA . Thus, increased expression of NR4A1 and elevated levels of RA in response to estrogen could promote cell proliferation and suppress pro-apoptosis activity. Proteolipid and DM20 encoded by the PLP1 gene through alternative splicing are major structural components of central nervous system myelin. It has been well established that steroid hormones such as estrogen and progesterone regulate the expression of myelin proteins such as proteolipid protein (reviewed in ). However, what roles PLP1 may play in the development of human uterine fibroids needs further study. Similarly we have little knowledge of what functions that RNase A family, 4 (RNASE4) plays in the tumor growth. It is worthwhile to note that directions of expression changes of ANXA1, NR4A1 and PLP1 were opposite from that of the estrogen treated rat uterus.
Human genetics studies have shown that 40–50% of human uterine fibroids display karyotypically detectable chromosomal abnormalities . Twenty percent of the abnormality is the characteristic translocation t(12:14) [58, 59]. The twelve estrogen-regulated genes identified in the present study did not map to this translocation. The most prominent predisposition genes involved in human uterine fibroids, HGMI(c) and HMGI (Y), account for nearly 50% of the genetic variation in human uterine fibroids . Dysregulation of these genes through chromosomal translation is a major event in uterine fibroid formation. Rearrangement of HMGI(C) and HMGI(Y) is also a very frequent event in many mesenchymal tumors, suggesting a critical role of the HMGI complex in tumorigenesis. The two key estrogen regulated pathways (e.g. RA and PPARγ) identified in the present study were both reported to be interacting with the HMG complex. For example, orchestrated action from PPARγ, HMGI(C), and other transcription factors is required in directing adipocyte differentiation . Altered activity of these transcription factors could lead to biased differentiation of adipocytes or even adipocyte hyperplasia. Moreover, the retinoic acid pathway could regulate or be regulated by HMGI(C) during neuroblastoma tumorigenesis. Both HMGI(C), and HMGI(Y) are expressed in neuroblastoma cell lines and tumors and they are regulated by RA both at the RNA and protein levels, and can affect the responsiveness of these cells to RA [61, 62]. A causal link has been proposed between HMGI(C) expression and RA induced growth arrest during tumorigenesis. Given the pivotal roles of the HMG complex in the fibroids and their interaction with PPARγ and RA pathways in controlling adipocyte growth and tumorigenesis of neuroblastoma, we speculate that estrogen may regulate fibroid growth through the PPARγ and RA pathways and their interaction with the HMGI(C) and HGMI(Y) complex. However, the direct link between HMG complex with RA and/or PPARγ in human uterine fibroids needs to be established experimentally, and is an area for future investigation.
In conclusion, integration of multiple DNA microarray studies through ortholog gene analysis identified twelve uterine fibroid disease genes that may respond to estrogen in the fibroid. Functional and pathway analyses suggested multiple molecular mechanisms for estrogen-dependent growth of human uterine fibroids: enhanced tumor cell survival by increased expression of PCP4 and decreased expression of TGF-β R2 and PTGER3 and the complex interplay among five distinct nuclear receptors (ER, RAR, RXR, NR4A1 and PPARγ) that may enhance tumor cell survival and growth. Fully understanding the exact molecular interactions among these genes requires further study to validate their role in uterine fibroids. This work provides direction for studies which could influence the future direction of therapeutic intervention for the disease.
We thank Dr. Rachelle Galvin for her thoughtful comments. We wish to acknowledge funding from Lilly Research Laboratories.
- Stewart EA: Uterine fibroids. Lancet. 2001, 357 (9252): 293-298. 10.1016/S0140-6736(00)03622-9.View ArticlePubMed
- Flake GP, Andersen J, Dixon D: Etiology and pathogenesis of uterine leiomyomas: a review. Environ Health Perspect. 2003, 111 (8): 1037-1054.PubMed CentralView ArticlePubMed
- Gambone JC, Reiter RC, Lench JB, Moore JG: The impact of a quality assurance process on the frequency and confirmation rate of hysterectomy. Am J Obstet Gynecol. 1990, 163 (2): 545-550.View ArticlePubMed
- Friedman AJ, Harrison-Atlas D, Barbieri RL, Benacerraf B, Gleason R, Schiff I: A randomized, placebo-controlled, double-blind study evaluating the efficacy of leuprolide acetate depot in the treatment of uterine leiomyomata. Fertil Steril. 1989, 51 (2): 251-256.PubMed
- Folkerd EJ, Newton CJ, Davidson K, Anderson MC, James VH: Aromatase activity in uterine leiomyomata. J Steroid Biochem. 1984, 20 (5): 1195-1200. 10.1016/0022-4731(84)90366-2.View ArticlePubMed
- Green S, Walter P, Kumar V, Krust A, Bornert JM, Argos P, Chambon P: Human oestrogen receptor cDNA: sequence, expression and homology to v-erb-A. Nature. 1986, 320 (6058): 134-139. 10.1038/320134a0.View ArticlePubMed
- Kumar V, Green S, Stack G, Berry M, Jin JR, Chambon P: Functional domains of the human estrogen receptor. Cell. 1987, 51 (6): 941-951. 10.1016/0092-8674(87)90581-2.View ArticlePubMed
- Mitchell DC, Ing NH: Estradiol stabilizes estrogen receptor messenger ribonucleic acid in sheep endometrium via discrete sequence elements in its 3'-untranslated region. Mol Endocrinol. 2003, 17 (4): 562-574. 10.1210/me.2002-0313.View ArticlePubMed
- Hayashi S, Sakamoto T, Inoue A, Yoshida N, Omoto Y, Yamaguchi Y: Estrogen and growth factor signaling pathway: basic approaches for clinical application. J Steroid Biochem Mol Biol. 2003, 86 (3-5): 433-442. 10.1016/S0960-0760(03)00354-6.View ArticlePubMed
- Fukuhara K, Kariya M, Kita M, Shime H, Kanamori T, Kosaka C, Orii A, Fujita J, Fujii S: Secreted frizzled related protein 1 is overexpressed in uterine leiomyomas, associated with a high estrogenic environment and unrelated to proliferative activity. J Clin Endocrinol Metab. 2002, 87 (4): 1729-1736. 10.1210/jc.87.4.1729.View ArticlePubMed
- Houston KD, Copland JA, Broaddus RR, Gottardis MM, Fischer SM, Walker CL: Inhibition of proliferation and estrogen receptor signaling by peroxisome proliferator-activated receptor gamma ligands in uterine leiomyoma. Cancer Res. 2003, 63 (6): 1221-1227.PubMed
- Tsibris JC, Porter KB, Jazayeri A, Tzimas G, Nau H, Huang H, Kuparadze K, Porter GW, O'Brien WF, Spellacy WN: Human uterine leiomyomata express higher levels of peroxisome proliferator-activated receptor gamma, retinoid X receptor alpha, and all-trans retinoic acid than myometrium. Cancer Res. 1999, 59 (22): 5737-5744.PubMed
- Shalon D, Smith SJ, Brown PO: A DNA microarray system for analyzing complex DNA samples using two-color fluorescent probe hybridization. Genome Res. 1996, 6 (7): 639-645.View ArticlePubMed
- Tsibris JC, Segars J, Coppola D, Mane S, Wilbanks GD, O'Brien WF, Spellacy WN: Insights from gene arrays on the development and growth regulation of uterine leiomyomata. Fertil Steril. 2002, 78 (1): 114-121. 10.1016/S0015-0282(02)03191-6.PubMed CentralView ArticlePubMed
- Helvering LM, Adrian MD, Geiser AG, Estrem ST, Wei T, Huang S, Chen P, Dow ER, Calley JN, Dodge JA, Grese TA, Jones SA, Halladay DL, Miles RR, Onyia JE, Ma YL, Sato M, Bryant HU: Differential effects of estrogen and raloxifene on messenger RNA and matrix metalloproteinase 2 activity in the rat uterus. Biol Reprod. 2005, 72 (4): 830-841. 10.1095/biolreprod.104.034595.View ArticlePubMed
- Jimenez JL, Mitchell MP, Sgouros JG: Microarray analysis of orthologous genes: conservation of the translational machinery across species at the sequence and expression level. Genome Biol. 2003, 4 (1): R4-10.1186/gb-2002-4-1-r4.PubMed CentralView ArticlePubMed
- Wang H, Mahadevappa M, Yamamoto K, Wen Y, Chen B, Warrington JA, Polan ML: Distinctive proliferative phase differences in gene expression in human myometrium and leiomyomata. Fertil Steril. 2003, 80 (2): 266-276. 10.1016/S0015-0282(03)00730-1.View ArticlePubMed
- Hoffman PJ, Milliken DB, Gregg LC, Davis RR, Gregg JP: Molecular characterization of uterine fibroids and its implication for underlying mechanisms of pathogenesis. Fertil Steril. 2004, 82 (3): 639-649. 10.1016/j.fertnstert.2004.01.047.View ArticlePubMed
- Benjamini Y, Hochberg: Controlling the false discovery rate:a practical and powerful approach to multiple testing. The Journal of Royal Statistical Society. 1995, 57 (1): 289-300.
- Edgar R, Domrachev M, Lash AE: Gene Expression Omnibus: NCBI gene expression and hybridization array data repository. Nucleic Acids Res. 2002, 30 (1): 207-210. 10.1093/nar/30.1.207.PubMed CentralView ArticlePubMed
- NetAffx [http://www.affymetrix.com/analysis/index.affx].
- Wheeler DL, Church DM, Federhen S, Lash AE, Madden TL, Pontius JU, Schuler GD, Schriml LM, Sequeira E, Tatusova TA, Wagner L: Database resources of the National Center for Biotechnology. Nucleic Acids Res. 2003, 31 (1): 28-33. 10.1093/nar/gkg033.PubMed CentralView ArticlePubMed
- Lee Y, Sultana R, Pertea G, Cho J, Karamycheva S, Tsai J, Parvizi B, Cheung F, Antonescu V, White J, Holt I, Liang F, Quackenbush J: Cross-referencing eukaryotic genomes: TIGR Orthologous Gene Alignments (TOGA). Genome Res. 2002, 12 (3): 493-502. 10.1101/gr.212002.PubMed CentralView ArticlePubMed
- Kent WJ: BLAT--the BLAST-like alignment tool. Genome Res. 2002, 12 (4): 656-664. 10.1101/gr.229202. Article published online before March 2002.PubMed CentralView ArticlePubMed
- Curwen V, Eyras E, Andrews TD, Clarke L, Mongin E, Searle SM, Clamp M: The Ensembl automatic gene annotation system. Genome Res. 2004, 14 (5): 942-950. 10.1101/gr.1858004.PubMed CentralView ArticlePubMed
- Al-Shahrour F, Diaz-Uriarte R, Dopazo J: FatiGO: a web tool for finding significant associations of Gene Ontology terms with groups of genes. Bioinformatics. 2004, 20 (4): 578-580. 10.1093/bioinformatics/btg455.View ArticlePubMed
- UCSC Genome Bioinformatics [http://genome.ucsc.edu/].
- Li XH, Ong DE: Cellular retinoic acid-binding protein II gene expression is directly induced by estrogen, but not retinoic acid, in rat uterus. J Biol Chem. 2003, 278 (37): 35819-35825. 10.1074/jbc.M302551200.View ArticlePubMed
- Li XH, Kakkad B, Ong DE: Estrogen directly induces expression of retinoic acid biosynthetic enzymes, compartmentalized between the epithelium and underlying stromal cells in rat uterus. Endocrinology. 2004, 145 (10): 4756-4762. 10.1210/en.2004-0514.View ArticlePubMed
- Mong JA, Devidze N, Frail DE, O'Connor LT, Samuel M, Choleris E, Ogawa S, Pfaff DW: Estradiol differentially regulates lipocalin-type prostaglandin D synthase transcript levels in the rodent brain: Evidence from high-density oligonucleotide arrays and in situ hybridization. Proc Natl Acad Sci U S A. 2003, 100 (1): 318-323. 10.1073/pnas.262663799.PubMed CentralView ArticlePubMed
- Mong JA, Devidze N, Goodwillie A, Pfaff DW: Reduction of lipocalin-type prostaglandin D synthase in the preoptic area of female mice mimics estradiol effects on arousal and sex behavior. Proc Natl Acad Sci U S A. 2003, 100 (25): 15206-15211. 10.1073/pnas.2436540100.PubMed CentralView ArticlePubMed
- Otsuki M, Gao H, Dahlman-Wright K, Ohlsson C, Eguchi N, Urade Y, Gustafsson JA: Specific regulation of lipocalin-type prostaglandin D synthase in mouse heart by estrogen receptor beta. Mol Endocrinol. 2003, 17 (9): 1844-1855. 10.1210/me.2003-0016.View ArticlePubMed
- Castro-Caldas M, Duarte CB, Carvalho AR, Lopes MC: 17beta-estradiol promotes the synthesis and the secretion of annexin I in the CCRF-CEM human cell line. Mediators Inflamm. 2001, 10 (5): 245-251. 10.1080/09629350120093713.PubMed CentralView ArticlePubMed
- Thota C, Yallampalli C: Progesterone upregulates calcitonin gene-related peptide and adrenomedullin receptor components and cyclic adenosine 3'5'-monophosphate generation in Eker rat uterine smooth muscle cell line. Biol Reprod. 2005, 72 (2): 416-422. 10.1095/biolreprod.104.033779.View ArticlePubMed
- Dong YL, Vegiraju S, Chauhan M, Yallampalli C: Expression of calcitonin gene-related peptide receptor components, calcitonin receptor-like receptor and receptor activity modifying protein 1, in the rat placenta during pregnancy and their cellular localization. Mol Hum Reprod. 2003, 9 (8): 481-490. 10.1093/molehr/gag058.View ArticlePubMed
- Cao X, Liu W, Lin F, Li H, Kolluri SK, Lin B, Han YH, Dawson MI, Zhang XK: Retinoid X receptor regulates Nur77/TR3-dependent apoptosis [corrected] by modulating its nuclear export and mitochondrial targeting. Mol Cell Biol. 2004, 24 (22): 9705-9725. 10.1128/MCB.24.22.9705-9725.2004.PubMed CentralView ArticlePubMed
- Cicatiello L, Sica V, Bresciani F, Weisz A: Identification of a specific pattern of "immediate-early" gene activation induced by estrogen during mitogenic stimulation of rat uterine cells. Receptor. 1993, 3 (1): 17-30.PubMed
- Giudice LC, Irwin JC, Dsupin BA, Pannier EM, Jin IH, Vu TH, Hoffman AR: Insulin-like growth factor (IGF), IGF binding protein (IGFBP), and IGF receptor gene expression and IGFBP synthesis in human uterine leiomyomata. Hum Reprod. 1993, 8 (11): 1796-1806.PubMed
- Adesanya OO, Zhou J, Bondy CA: Sex steroid regulation of insulin-like growth factor system gene expression and proliferation in primate myometrium. J Clin Endocrinol Metab. 1996, 81 (5): 1967-1974. 10.1210/jc.81.5.1967.PubMed
- Norstedt G, Levinovitz A, Eriksson H: Regulation of uterine insulin-like growth factor I mRNA and insulin-like growth factor II mRNA by estrogen in the rat. Acta Endocrinol (Copenh). 1989, 120 (4): 466-472.
- Kawamoto S, Matsumoto Y, Mizuno K, Okubo K, Matsubara K: Expression profiles of active genes in human and mouse livers. Gene. 1996, 174 (1): 151-158. 10.1016/0378-1119(96)00512-4.View ArticlePubMed
- Rocca-Serra P, Brazma A, Parkinson H, Sarkans U, Shojatalab M, Contrino S, Vilo J, Abeygunawardena N, Mukherjee G, Holloway E, Kapushesky M, Kemmeren P, Lara GG, Oezcimen A, Sansone SA: ArrayExpress: a public database of gene expression data at EBI. C R Biol. 2003, 326 (10-11): 1075-1078. 10.1016/j.crvi.2003.09.026.View ArticlePubMed
- Irie A, Sugimoto Y, Namba T, Harazono A, Honda A, Watabe A, Negishi M, Narumiya S, Ichikawa A: Third isoform of the prostaglandin-E-receptor EP3 subtype with different C-terminal tail coupling to both stimulation and inhibition of adenylate cyclase. Eur J Biochem. 1993, 217 (1): 313-318. 10.1111/j.1432-1033.1993.tb18248.x.View ArticlePubMed
- Shoji Y, Takahashi M, Kitamura T, Watanabe K, Kawamori T, Maruyama T, Sugimoto Y, Negishi M, Narumiya S, Sugimura T, Wakabayashi K: Downregulation of prostaglandin E receptor subtype EP3 during colon cancer development. Gut. 2004, 53 (8): 1151-1158. 10.1136/gut.2003.028787.PubMed CentralView ArticlePubMed
- Barlow J, Yandell D, Weaver D, Casey T, Plaut K: Higher stromal expression of transforming growth factor-beta type II receptors is associated with poorer prognosis breast tumors. Breast Cancer Res Treat. 2003, 79 (2): 149-159. 10.1023/A:1023918026437.View ArticlePubMed
- Erhardt JA, Legos JJ, Johanson RA, Slemmon JR, Wang X: Expression of PEP-19 inhibits apoptosis in PC12 cells. Neuroreport. 2000, 11 (17): 3719-3723. 10.1097/00001756-200011270-00026.View ArticlePubMed
- Beltowski J, Jamroz A: Adrenomedullin--what do we know 10 years since its discovery?. Pol J Pharmacol. 2004, 56 (1): 5-27.PubMed
- Urade Y, Hayaishi O: Biochemical, structural, genetic, physiological, and pathophysiological features of lipocalin-type prostaglandin D synthase. Biochim Biophys Acta. 2000, 1482 (1-2): 259-271.View ArticlePubMed
- Flower RJ, Rothwell NJ: Lipocortin-1: cellular mechanisms and clinical relevance. Trends Pharmacol Sci. 1994, 15 (3): 71-76. 10.1016/0165-6147(94)90281-X.View ArticlePubMed
- Parente L, Solito E: Annexin 1: more than an anti-phospholipase protein. Inflamm Res. 2004, 53 (4): 125-132. 10.1007/s00011-003-1235-z.View ArticlePubMed
- Duester G: Families of retinoid dehydrogenases regulating vitamin A function: production of visual pigment and retinoic acid. Eur J Biochem. 2000, 267 (14): 4315-4324. 10.1046/j.1432-1327.2000.01497.x.View ArticlePubMed
- Yuan GJ, Zhang ML, Gong ZJ: Effects of PPARg agonist pioglitazone on rat hepatic fibrosis. World J Gastroenterol. 2004, 10 (7): 1047-1051.PubMed
- Shimada T, Kojima K, Yoshiura K, Hiraishi H, Terano A: Characteristics of the peroxisome proliferator activated receptor gamma (PPARgamma) ligand induced apoptosis in colon cancer cells. Gut. 2002, 50 (5): 658-664. 10.1136/gut.50.5.658.PubMed CentralView ArticlePubMed
- Kojima K, Shimada T, Mitobe Y, Yoshiura K, Hiraishi H, Terano A: Effect of PPARgamma ligands on the viability of gastric epithelial cells. Aliment Pharmacol Ther. 2002, 16 Suppl 2: 67-73. 10.1046/j.1365-2036.16.s2.16.x.View ArticlePubMed
- Elizondo G, Corchero J, Sterneck E, Gonzalez FJ: Feedback inhibition of the retinaldehyde dehydrogenase gene ALDH1 by retinoic acid through retinoic acid receptor alpha and CCAAT/enhancer-binding protein beta. J Biol Chem. 2000, 275 (50): 39747-39753. 10.1074/jbc.M004987200.View ArticlePubMed
- Kolluri SK, Bruey-Sedano N, Cao X, Lin B, Lin F, Han YH, Dawson MI, Zhang XK: Mitogenic effect of orphan receptor TR3 and its regulation by MEKK1 in lung cancer cells. Mol Cell Biol. 2003, 23 (23): 8651-8667. 10.1128/MCB.23.23.8651-8667.2003.PubMed CentralView ArticlePubMed
- Chan JR, Rodriguez-Waitkus PM, Ng BK, Liang P, Glaser M: Progesterone synthesized by Schwann cells during myelin formation regulates neuronal gene expression. Mol Biol Cell. 2000, 11 (7): 2283-2295.PubMed CentralView ArticlePubMed
- Ligon AH, Morton CC: Genetics of uterine leiomyomata. Genes Chromosomes Cancer. 2000, 28 (3): 235-245. 10.1002/1098-2264(200007)28:3<235::AID-GCC1>3.0.CO;2-7.View ArticlePubMed
- Ligon AH, Morton CC: Leiomyomata: heritability and cytogenetic studies. Hum Reprod Update. 2001, 7 (1): 8-14. 10.1093/humupd/7.1.8.View ArticlePubMed
- Auwerx J, Martin G, Guerre-Millo M, Staels B: Transcription, adipocyte differentiation, and obesity. J Mol Med. 1996, 74 (7): 347-352. 10.1007/s001090050036.View ArticlePubMed
- Giannini G, Di Marcotullio L, Ristori E, Zani M, Crescenzi M, Scarpa S, Piaggio G, Vacca A, Peverali FA, Diana F, Screpanti I, Frati L, Gulino A: HMGI(Y) and HMGI-C genes are expressed in neuroblastoma cell lines and tumors and affect retinoic acid responsiveness. Cancer Res. 1999, 59 (10): 2484-2492.PubMed
- Giannini G, Kim CJ, Di Marcotullio L, Manfioletti G, Cardinali B, Cerignoli F, Ristori E, Zani M, Frati L, Screpanti I, Guilino A: Expression of the HMGI(Y) gene products in human neuroblastic tumours correlates with differentiation status. Br J Cancer. 2000, 83 (11): 1503-1509. 10.1054/bjoc.2000.1494.PubMed CentralView ArticlePubMed
- Rexer BN, Ong DE: A novel short-chain alcohol dehydrogenase from rats with retinol dehydrogenase activity, cyclically expressed in uterine epithelium. Biol Reprod. 2002, 67 (5): 1555-1564. 10.1095/biolreprod.102.007021.View ArticlePubMed
- Uemura H, Mizokami A, Chang C: Identification of a new enhancer in the promoter region of human TR3 orphan receptor gene. A member of steroid receptor superfamily. J Biol Chem. 1995, 270 (10): 5427-5433. 10.1074/jbc.270.10.5427.View ArticlePubMed
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6874/7/5/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.