Identification and characterization of progesterone- and estrogen-regulated MicroRNAs in mouse endometrial epithelial cells

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This study identified 146 progesterone-upregulated microRNAs in mouse endometrial epithelial cells, with miRNA-145a potentially mediating the antiproliferative effects of progesterone against estrogen.

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This study utilized high-throughput sequencing to identify microRNAs regulated by progesterone and estrogen in the endometrial epithelium of ovariectomized mice. The researchers found that progesterone treatment significantly upregulated 146 mature microRNAs, which were involved in various biological processes including cell proliferation control. Specifically, miR-145a was highlighted as a potential mediator of progesterone’s antiproliferative effects on these cells, offering insight into how progesterone antagonizes estrogen-driven growth. Relevance to endometriosis: listed among references for hormonal regulation mechanisms, though the paper's main focus is normal mouse uterine physiology rather than pathological conditions.

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Abstract

In endometrial epithelial cells, progesterone (P4) functions in regulating the cell structure and opposing the effects of estrogen. However, the mechanisms of P4 that oppose the effects of estrogen remain unclear. MicroRNAs (miRNAs) are important posttranscriptional regulators that are involved in various physiological and pathological processes. Whether P4 directly induces miRNA expression to antagonize estrogen in endometrial epithelium is unclear. In this study, total RNAs were extracted from endometrial epithelium of ovariectomized mice, which were treated with estrogen alone or a combination of estrogen and P4. MicroRNA high-throughput sequencing with bioinformatics analysis was used to identify P4-induced miRNAs, predict their potential target genes, and analyze their possible biological functions. We observed that 146 mature miRNAs in endometrial epithelial cells were significantly upregulated by P4. These miRNAs were extensively involved in multiple biological processes. The miRNA-145a demonstrated a possible function in the antiproliferative action of P4 on endometrial epithelial cells.
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Abstract

In endometrial epithelial cells, progesterone (P4) functions in regulating the cell structure and opposing the effects of estrogen. However, the mechanisms of P4 that oppose the effects of estrogen remain unclear. MicroRNAs (miRNAs) are important posttranscriptional regulators that are involved in various physiological and pathological processes. Whether P4 directly induces miRNA expression to antagonize estrogen in endometrial epithelium is unclear. In this study, total RNAs were extracted from endometrial epithelium of ovariectomized mice, which were treated with estrogen alone or a combination of estrogen and P4. MicroRNA high-throughput sequencing with bioinformatics analysis was used to identify P4-induced miRNAs, predict their potential target genes, and analyze their possible biological functions. We observed that 146 mature miRNAs in endometrial epithelial cells were significantly upregulated by P4. These miRNAs were extensively involved in multiple biological processes. The miRNA-145a demonstrated a possible function in the antiproliferative action of P4 on endometrial epithelial cells. Similar content being viewed by others

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The micro-RNA.org resource: targets and expression. Nucleic Acids Res. 2008;36 (Database Issue): D149–53. Author information Authors and Affiliations Corresponding author Rights and permissions About this article Cite this article Yuan, Dz., Yu, Ll., Qu, T. et al. Identification and Characterization of Progesterone- and Estrogen-Regulated MicroRNAs in Mouse Endometrial Epithelial Cells. Reprod. Sci. 22, 223–234 (2015). https://doi.org/10.1177/1933719114537714 Published: Issue date: DOI: https://doi.org/10.1177/1933719114537714

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MeSH descriptors

Endometrium Epithelial Cells Estrogens MicroRNAs Progesterone Animals Cell Proliferation Cell Proliferation Computational Biology Endometrium Endometrium Epithelial Cells Epithelial Cells Estrogens Female Gene Expression Profiling Gene Expression Regulation Gene Library Gene Regulatory Networks High-Throughput Nucleotide Sequencing

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