Knockdown of circ_0075503 suppresses cell migration and invasion by regulating miR-15a-5p and KLF12 in endometriosis

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This study found that knocking down circ_0075503 suppressed estradiol-induced migration and invasion of endometrial stromal cells by regulating the miR-15a-5p/KLF12 axis.

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This study investigated the circRNA circ_0075503 in endometriosis, examining paired ectopic versus eutopic endometrial tissues (n=30) and estradiol (E2)-stimulated primary eutopic endometrial stromal cells as an in vitro model. circ_0075503 expression was elevated in ectopic tissue and ectopic-like stromal cells, and its knockdown suppressed E2-induced increases in cell viability, migration, and invasion. Mechanistically, circ_0075503 acted as a sponge for miR-15a-5p, with miR-15a-5p targeting KLF12, and the effects of circ_0075503 knockdown on migration/invasion were reversed by miR-15a-5p inhibition; independently, miR-15a-5p inhibited E2-driven migration/invasion via KLF12. A limitation explicitly implied by the design is reliance on in vitro stromal cell assays and an estradiol stimulation model rather than direct in vivo functional validation. This paper is centrally about endometriosis — it focuses on circ_0075503 regulating the miR-15a-5p/KLF12 axis to control stromal cell migration and invasion relevant to lesion establishment.

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Abstract

Endometriosis is an estrogen-dependent disease. Several researches have reported the dysregulated circular RNAs (circRNAs) in endometriosis, whereas the functions of circRNAs are largely unknown. This study aims to explore the role and mechanism of circ_0075503 in migration and invasion of eutopic endometrial stromal cells. 30 paired ectopic and eutopic endometrium tissues were collected from patients with endometriosis. And primary endometrial stromal cells (ESCs) were stimulated with estradiol (E2) to establish the in vitro cellular model of endometriosis. The levels of circ_0075503, miR-15a-5p and Krüppel-like factor 12 (KLF12) were measured by quantitative reverse transcription polymerase chain reaction or western blot assays. Cell viability, migration and invasion were examined via 3-(4, 5-dimethyl-2-thiazolyl)-2, 5-diphenyl-2-H-tetrazolium bromide, transwell assay or western blot assays. The target relationship between miR-15a-5p and circ_0075503 or KLF12 was analyzed by dual-luciferase reporter assay and RNA Immunoprecipitation (RIP) assay. Circ_0075503 expression was elevated in ectopic endometrium and ectopic ESCs. Down-regulation of circ_0075503 suppressed E2-induced promotion of cell viability, migration and invasion in eutopic ESCs. Circ_0075503 could act as a sponge for miR-15a-5p, and KLF12 was targeted by miR-15a-5p. Inhibition of miR-15a-5p reversed the effects of circ_0075503 knockdown on E2-treated ESCs migration and invasion. Besides, miR-15a-5p repressed E2-induced promotion effects on cell migration and invasion via targeting KLF12. Circ_0075503 could regulate KLF12 expression by sponging miR-15a-5p. Knockdown of circ_0075503 inhibited E2-induced enhancement of cell migration and invasion in eutopic ESCs by regulating miR-15a-5p/KLF12 axis, indicating a novel target for the treatment of endometriosis.
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Abstract

Endometriosis is an estrogen-dependent disease. Several researches have reported the dysregulated circular RNAs (circRNAs) in endometriosis, whereas the functions of circRNAs are largely unknown. This study aims to explore the role and mechanism of circ_0075503 in migration and invasion of eutopic endometrial stromal cells. 30 paired ectopic and eutopic endometrium tissues were collected from patients with endometriosis. And primary endometrial stromal cells (ESCs) were stimulated with estradiol (E2) to establish the in vitro cellular model of endometriosis. The levels of circ_0075503, miR-15a-5p and Krüppel-like factor 12 (KLF12) were measured by quantitative reverse transcription polymerase chain reaction or western blot assays. Cell viability, migration and invasion were examined via 3-(4, 5-dimethyl-2-thiazolyl)-2, 5-diphenyl-2-H-tetrazolium bromide, transwell assay or western blot assays. The target relationship between miR-15a-5p and circ_0075503 or KLF12 was analyzed by dual-luciferase reporter assay and RNA Immunoprecipitation (RIP) assay. Circ_0075503 expression was elevated in ectopic endometrium and ectopic ESCs. Down-regulation of circ_0075503 suppressed E2-induced promotion of cell viability, migration and invasion in eutopic ESCs. Circ_0075503 could act as a sponge for miR-15a-5p, and KLF12 was targeted by miR-15a-5p. Inhibition of miR-15a-5p reversed the effects of circ_0075503 knockdown on E2-treated ESCs migration and invasion. Besides, miR-15a-5p repressed E2-induced promotion effects on cell migration and invasion via targeting KLF12. Circ_0075503 could regulate KLF12 expression by sponging miR-15a-5p. Knockdown of circ_0075503 inhibited E2-induced enhancement of cell migration and invasion in eutopic ESCs by regulating miR-15a-5p/KLF12 axis, indicating a novel target for the treatment of endometriosis. Similar content being viewed by others Data availability The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request. Abbreviations - ESCs: - Endometrial stromal cells - KLF12: - Krüppel-like factor 12

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Acknowledgements

None. Funding None. Author information Authors and Affiliations Contributions DL conceived and designed the present study. YL, MC, FY preformed the experiment. SY was responsible for the data analysis and performed data interpretation. DL wrote the paper. DL and SY revised the manuscript. Corresponding author Ethics declarations Conflict of interest The authors declare that they have no financial conflicts of interest. Additional information Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Supplementary Information Below is the link to the electronic supplementary material. Rights and permissions About this article Cite this article Liu, D., Liang, Y., Chen, M. et al. Knockdown of circ_0075503 suppresses cell migration and invasion by regulating miR-15a-5p and KLF12 in endometriosis. Mol Cell Biochem 476, 3845–3856 (2021). https://doi.org/10.1007/s11010-021-04202-5 Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s11010-021-04202-5

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endometriosis

MeSH descriptors

Cell Movement Endometriosis Gene Knockdown Techniques Kruppel-Like Transcription Factors MicroRNAs RNA, Circular Adult Endometriosis Endometriosis Female Humans Kruppel-Like Transcription Factors Kruppel-Like Transcription Factors MicroRNAs MicroRNAs Middle Aged RNA, Circular RNA, Circular Stromal Cells Stromal Cells

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