MiR-199a-5p Targets ZEB1 to Inhibit the Epithelial-Mesenchymal Transition of Ovarian Ectopic Endometrial Stromal Cells Via PI3K/Akt/mTOR Signal Pathway In Vitro and In Vivo

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MiR-199a-5p inhibits ectopic endometrial stromal cell epithelial-mesenchymal transition by targeting ZEB1 and the PI3K/Akt/mTOR pathway, both in vitro and in vivo.

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The study examined how microRNA-199a-5p affects invasion, migration, and epithelial-mesenchymal transition (EMT) in ovarian ectopic endometrial stromal cells (EcSCs), using EcSCs versus control stromal cells in vitro and an endometriosis rat model in vivo. miR-199a-5p was found lower in EcSCs than in controls, and miR-199a-5p mimic suppressed EcSC invasion/migration and EMT, with ZEB1 identified as a direct target via bioinformatics and luciferase reporter assay; overexpression of pcDNA3.1-ZEB1 weakened these effects. The paper reports that miR-199a-5p mimic inactivated PI3K/Akt/mTOR signaling and that adding IGF-1 abolished miR-199a-5p–mediated endometriosis progression changes, while miR-199a-5p agomir also reduced VEGF and EMT marker expression and inactivated PI3K/Akt/mTOR in vivo. The paper does not explicitly state a specific limitation in the abstract. This paper is centrally about endometriosis — it tests miR-199a-5p targeting ZEB1 to inhibit EMT and progression of endometriosis through PI3K/Akt/mTOR in vitro and in vivo.

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Abstract

Endometriosis (Ems) is a common gynecological disease with the characteristics of infertility, pelvic pain, and sexual intercourse difficulty. Our present study aimed to investigate the effect of miR-199a-5p on cell mobility and epithelial-mesenchymal transition (EMT) in Ems. Ectopic endometrial stromal cells (EcSCs) and control endometrial stromal cells (CSCs) were isolated in our in vitro experiments. The level of miR-199a-5p in EcSCs was found much lower than that in CSCs. Besides, miR-199a-5p mimic suppressed the invasion and migration ability of EcSCs. At the same time, EMT was also found to be suppressed by miR-199a-5p mimic in EcSCs. Our further bioinformatics analysis and luciferase reporter assay revealed that ZEB1, a marker of EMT, was a direct target of miR-199a-5p. In addition, the combination of pcDNA3.1-ZEB1 weakened the inhibiting effect of miR-199a-5p mimic on the mobility and EMT of EcSCs. What is more, the PI3K/Akt/mTOR signal pathway was demonstrated to be inactivated by miR-199a-5p mimic. And then, the inducer of PI3K/Akt/mTOR signal pathway, IGF-1, abolished the effect of miR-199a-5p mimic on Ems progression. At last, an Ems rat model was established, and we found that miR-199a-5p agomir effectively suppressed the expression of vascular endothelial growth factor (VEGF) and EMT in vivo. The PI3K/Akt/mTOR signal pathway was also inactivated by miR-199a-5p agomir in our Ems rat model. Taken together, we concluded that miR-199a-5p targeted ZEB1 to inhibit the EMT of ovarian ectopic endometrial stromal cells via PI3K/Akt/mTOR signal pathway in vitro and in vivo, advancing our understanding of miR-199a-5p as regulators of Ems progression and making contribution to the treatment of Ems.
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Abstract

Endometriosis (Ems) is a common gynecological disease with the characteristics of infertility, pelvic pain, and sexual intercourse difficulty. Our present study aimed to investigate the effect of miR-199a-5p on cell mobility and epithelial-mesenchymal transition (EMT) in Ems. Ectopic endometrial stromal cells (EcSCs) and control endometrial stromal cells (CSCs) were isolated in our in vitro experiments. The level of miR-199a-5p in EcSCs was found much lower than that in CSCs. Besides, miR-199a-5p mimic suppressed the invasion and migration ability of EcSCs. At the same time, EMT was also found to be suppressed by miR-199a-5p mimic in EcSCs. Our further bioinformatics analysis and luciferase reporter assay revealed that ZEB1, a marker of EMT, was a direct target of miR-199a-5p. In addition, the combination of pcDNA3.1-ZEB1 weakened the inhibiting effect of miR-199a-5p mimic on the mobility and EMT of EcSCs. What is more, the PI3K/Akt/mTOR signal pathway was demonstrated to be inactivated by miR-199a-5p mimic. And then, the inducer of PI3K/Akt/mTOR signal pathway, IGF-1, abolished the effect of miR-199a-5p mimic on Ems progression. At last, an Ems rat model was established, and we found that miR-199a-5p agomir effectively suppressed the expression of vascular endothelial growth factor (VEGF) and EMT in vivo. The PI3K/Akt/mTOR signal pathway was also inactivated by miR-199a-5p agomir in our Ems rat model. Taken together, we concluded that miR-199a-5p targeted ZEB1 to inhibit the EMT of ovarian ectopic endometrial stromal cells via PI3K/Akt/mTOR signal pathway in vitro and in vivo, advancing our understanding of miR-199a-5p as regulators of Ems progression and making contribution to the treatment of Ems. Similar content being viewed by others Abbreviations - Ems: - Endometriosis - EcSCs: - Ectopic endometrial stromal cells - CSCs: - Control endometrial stromal cells - EMT: - Epithelial-mesenchymal transition - VEGF: - Vascular endothelial growth factor

References

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MiR-199a-5p Targets ZEB1 to Inhibit the Epithelial-Mesenchymal Transition of Ovarian Ectopic Endometrial Stromal Cells Via PI3K/Akt/mTOR Signal Pathway In Vitro and In Vivo. Reprod. Sci. 27, 110–118 (2020). https://doi.org/10.1007/s43032-019-00016-5 Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s43032-019-00016-5

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endometriosis

MeSH descriptors

Endometriosis Epithelial-Mesenchymal Transition MicroRNAs Signal Transduction Stromal Cells Zinc Finger E-box-Binding Homeobox 1 Adult Animals Cell Proliferation Disease Models, Animal Disease Progression Endometriosis Epithelial-Mesenchymal Transition Female Humans MicroRNAs Phosphatidylinositol 3-Kinases Phosphatidylinositol 3-Kinases Proto-Oncogene Proteins c-akt Proto-Oncogene Proteins c-akt

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