Ami R Zota, Ruth J Geller, Brianna N VanNoy, Cherie Q Marfori, Sana Tabbara, Lisa Y Hu, Andrea A Baccarelli, Gaby N Moawad
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We quantified expression levels of 754 miRNAs in fibroid tumor samples and analyzed spot urine samples for phthalate metabolites collected from 45 pre-menopausal women undergoing surgery for fibroid treatment at an academic hospital. Associations between miRNA levels in fibroids and phthalate biomarkers were evaluated using linear regression adjusting for age, race/ethnicity, and body mass index (BMI). Statistical tests were adjusted for multiple comparisons. We also performed in silico Ingenuity Pathway Analysis to identify the biological pathways that are regulated by phthalate-associated miRNAs. Mono-hydroxybutyl phthalate and mono(2-ethyl-5-hydroxyhexyl) phthalate were positively associated with miR-10a-5p (β = 0.76, 95% CI = [0.40, 1.11]) and miR-577 (β = 1.06, 95% CI = [0.53, 1.59]), respectively. A total of 8 phthalate-miRNA associations varied by race/ethnicity (q<sub>interaction</sub> < 0.10). Pathway analysis revealed that mRNA gene targets of phthalate-associated miRNAs were significantly associated with multiple fibroid-related processes including angiogenesis, apoptosis, and proliferation of connective tissues. Collectively, these data suggest that exposures to some phthalates are associated with miRNA in fibroids, and that associations may vary by race/ethnicity. 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引用次数: 24
摘要
邻苯二甲酸酯与多种不良生殖结果相关,包括子宫平滑肌瘤(肌瘤)风险增加。邻苯二甲酸盐可以与表观遗传修饰相互作用,包括microRNAs (miRNAs),这有助于调节对肌瘤发病至关重要的过程。然而,之前没有研究检测邻苯二甲酸盐对肌瘤中miRNA表达的影响。我们进行了一项初步的横断面研究,以检查子宫肌瘤中邻苯二甲酸盐暴露与miRNA表达水平之间的关系,并探讨种族/民族对潜在影响的影响。我们量化了子宫肌瘤样本中754种mirna的表达水平,并分析了在一家学术医院接受子宫肌瘤手术治疗的45名绝经前妇女的尿液样本中邻苯二甲酸盐代谢物的斑点。使用线性回归评估肌瘤中miRNA水平与邻苯二甲酸酯生物标志物之间的关系,调整年龄、种族/民族和体重指数(BMI)。统计检验对多重比较进行了调整。我们还进行了硅独创性途径分析,以确定受邻苯二甲酸盐相关mirna调节的生物学途径。邻苯二甲酸单羟基丁酯和邻苯二甲酸单(2-乙基-5-羟基己基)分别与miR-10a-5p (β = 0.76, 95% CI =[0.40, 1.11])和miR-577 (β = 1.06, 95% CI =[0.53, 1.59])呈正相关。共有8种邻苯二甲酸盐- mirna关联因种族/民族而异(相互作用)
Phthalate Exposures and MicroRNA Expression in Uterine Fibroids: The FORGE Study.
Phthalates are associated with multiple, adverse reproductive outcomes including increased risk of uterine leiomyoma (fibroids). Phthalates can interact with epigenetic modifications including microRNAs (miRNAs), which help regulate processes crucial to fibroid pathogenesis. However, no prior study has examined the influence of phthalates on miRNA expression in fibroid tumors. We conducted a preliminary, cross-sectional study to examine the associations between phthalate exposures and miRNA expression levels in fibroid tumors and to explore potential effect modification by race/ethnicity. We quantified expression levels of 754 miRNAs in fibroid tumor samples and analyzed spot urine samples for phthalate metabolites collected from 45 pre-menopausal women undergoing surgery for fibroid treatment at an academic hospital. Associations between miRNA levels in fibroids and phthalate biomarkers were evaluated using linear regression adjusting for age, race/ethnicity, and body mass index (BMI). Statistical tests were adjusted for multiple comparisons. We also performed in silico Ingenuity Pathway Analysis to identify the biological pathways that are regulated by phthalate-associated miRNAs. Mono-hydroxybutyl phthalate and mono(2-ethyl-5-hydroxyhexyl) phthalate were positively associated with miR-10a-5p (β = 0.76, 95% CI = [0.40, 1.11]) and miR-577 (β = 1.06, 95% CI = [0.53, 1.59]), respectively. A total of 8 phthalate-miRNA associations varied by race/ethnicity (qinteraction < 0.10). Pathway analysis revealed that mRNA gene targets of phthalate-associated miRNAs were significantly associated with multiple fibroid-related processes including angiogenesis, apoptosis, and proliferation of connective tissues. Collectively, these data suggest that exposures to some phthalates are associated with miRNA in fibroids, and that associations may vary by race/ethnicity. Validation of these findings may provide insight into mechanisms underlying associations between phthalates and fibroids and contribute to novel hypotheses regarding racial/ethnic disparities in fibroids.