Department of Obstetrics, Gynecology and Molecular Reproductive Science, Yokohama City University Graduate School of Medicine, Kanazawa-ku, Yokohama, Kanagawa, Japan.
Department of Obstetrics, Gynecology and Molecular Reproductive Science, Yokohama City University Graduate School of Medicine, Kanazawa-ku, Yokohama, Kanagawa, Japan.
Fertil Steril. 2019 Jan;111(1):178-185. doi: 10.1016/j.fertnstert.2018.09.014. Epub 2018 Dec 13.
To determine factors that impact erythropoietin (EPO) production in leiomyomas. We have previously implicated EPO production in promoting the growth of some leiomyomas.
The relationship between EPO messenger RNA (mRNA) expression and MED12 gene mutations or mRNA expression levels of high-mobility group AT-hook (HMGA) 1 and HMGA2 were analyzed. Effects of 10 M 17β-E on EPO mRNA expression were evaluated using leiomyoma cells grown in primary cultures.
Graduate school of medicine.
PATIENT(S): Patients with leiomyoma.
INTERVENTION(S): We used tissue samples and clinical data of 108 patients with leiomyomas to analyze the relation between EPO mRNA expression and MED12 mutation. Tissue samples from another 10 patients with leiomyomas were collected for in vitro experimentation using primary cultures of leiomyoma and myometrial cells.
MAIN OUTCOME MEASURE(S): Relations between EPO mRNA expression, MED12 exon 2 mutation, and HMGA1/HMGA2 mRNA expression levels in leiomyoma samplings, in addition to effects of estrogen (E) on EPO mRNA expression in cultures of leiomyoma cells.
RESULT(S): The EPO mRNA level was threefold higher in leiomyomas with wild-type (vs. mutated) MED12 genes. There was no correlation between EPO and HMGA1 or HMGA2 mRNA expression levels. In wild-type MED12 leiomyomas only, E treatment produced a twofold increase in EPO mRNA expression, whereas mutated MED12 leiomyomas were unaffected.
CONCLUSION(S): The EPO mRNA expression increased significantly after E treatment only in leiomyomas lacking MED12 mutations. In conjunction with prior evidence linking EPO mRNA expression levels and tumor size, E-stimulated EPO mRNA expression may explain the marked growth disparities seen in these tumors.
确定影响子宫肌瘤中促红细胞生成素 (EPO) 产生的因素。我们之前曾暗示 EPO 的产生有助于促进一些子宫肌瘤的生长。
分析 EPO 信使 RNA (mRNA) 表达与 MED12 基因突变或高迁移率族 AT 钩 (HMGA) 1 和 HMGA2 的 mRNA 表达水平之间的关系。使用原代培养的子宫肌瘤细胞评估 10 μM 17β-E 对 EPO mRNA 表达的影响。
医学院研究生院。
子宫肌瘤患者。
我们使用 108 例子宫肌瘤患者的组织样本和临床数据来分析 EPO mRNA 表达与 MED12 突变之间的关系。另外,还收集了 10 例子宫肌瘤患者的组织样本,用于子宫肌瘤和子宫肌细胞原代培养的体外实验。
子宫肌瘤组织中 EPO mRNA 表达、MED12 外显子 2 突变与 HMGA1/HMGA2 mRNA 表达水平之间的关系,以及 E 在培养的子宫肌瘤细胞中对 EPO mRNA 表达的影响。
野生型(vs. 突变型)MED12 基因的子宫肌瘤中 EPO mRNA 水平高 3 倍。EPO 与 HMGA1 或 HMGA2 mRNA 表达水平之间没有相关性。仅在野生型 MED12 子宫肌瘤中,E 处理后 EPO mRNA 表达增加了两倍,而突变型 MED12 子宫肌瘤则不受影响。
只有在缺乏 MED12 突变的子宫肌瘤中,E 处理后 EPO mRNA 表达显著增加。结合先前将 EPO mRNA 表达水平与肿瘤大小联系起来的证据,E 刺激的 EPO mRNA 表达可能解释了这些肿瘤中明显的生长差异。