Cited by 357Endometriosis Research and TreatmentMicroRNA in disease regulationExtracellular vesicles in disease

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MicroRNA-Regulated Pathways Associated with Endometriosis

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Ohlsson Teague, E. Maria C., Van der Hoek, Kylie H., Van der Hoek, Mark B., Perry, Naomi, Wagaarachchi, Prabhath, Robertson, Sarah A., Print, Cristin G., Hull, Louise M.·2009·Molecular Endocrinology

DOI 10.1210/me.2008-0387PMC PMC5419313

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Abstract

Endometriosis is a prevalent gynecological disease characterized by growth of endometriotic tissue outside the uterine cavity. MicroRNAs (miRNAs) are naturally occurring posttranscriptional regulatory molecules that potentially play a role in endometriotic lesion development. We assessed miRNA expression by microarray analysis in paired ectopic and eutopic endometrial tissues and identified 14 up-regulated (miR-145, miR-143, miR-99a, miR-99b, miR-126, miR-100, miR-125b, miR-150, miR-125a, miR-223, miR-194, miR-365, miR-29c and miR-1) and eight down-regulated (miR-200a, miR-141, miR-200b, miR-142-3p, miR-424, miR-34c, miR-20a and miR-196b) miRNAs. The differential expression of six miRNAs was confirmed by quantitative RT-PCR. An in silico analysis identified 3851 mRNA transcripts as putative targets of the 22 miRNAs. Of these predicted targets, 673 were also differentially expressed in ectopic vs. eutopic endometrial tissue, as determined by microarray. Functional analysis suggested that the 673 miRNA targets constitute molecular pathways previously associated with endometriosis, including c-Jun, CREB-binding protein, protein kinase B (Akt), and cyclin D1 (CCND1) signaling. These pathways appeared to be regulated both transcriptionally as well as by miRNAs at posttranscriptional level. These data are a rich and novel resource for endometriosis and miRNA research and suggest that the 22 miRNAs and their cognate mRNA target sequences constitute pathways that promote endometriosis. Accordingly, miRNAs are potential therapeutic targets for treating this disease.

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The expression profile of micro-RNA in endometrium and endometriosis and the influence of ovarian steroids on their expression
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Authors: Ohlsson Teague, E. M. C., Van der Hoek, K. H., Van der Hoek, M. B., Perry, N., Wagaarachchi, P., Robertson, S. A., Print, C. G., & Hull, L. M.
Affiliations: The University of Adelaide (AU)
Women's and Children's Hospital (AU)
University of Auckland (NZ)
ORCID: Robertson, Sarah A.
Print, Cristin G.
Venue: Molecular Endocrinology
Publisher: The Endocrine Society
Published: 2009-02
Volume: 23
Issue: 2
Pages: 265-275
ISSN: 0888-8809 (ISSN-L)
1944-9917
DOI: 10.1210/me.2008-0387
PMC: PMC5419313
OpenAlex: W1993162436
Cited by: 357
References: 65
Citations by year: 2026: 4 · 2025: 16 · 2024: 17 · 2023: 11 · 2022: 24 · 2021: 21 · 2020: 22 · 2019: 22 · 2018: 26 · 2017: 25 · 2016: 23 · 2015: 22 · 2014: 20 · 2013: 25 · 2012: 18
FWCI: 23.24
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: Molecular Endocrinology (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Adelaide Research & Scholarship (AR&S) (University of Adelaide) (submittedVersion)
ResearchSpace (University of Auckland) (submittedVersion)
Topics: Health Sciences › Medicine › Reproductive Medicine › Endometriosis Research and Treatment
Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
Keywords: endometriosis, microRNA, miRNA expression profiling, ectopic endometrium, eutopic endometrium, miRNA target prediction, CREB-binding protein, Akt signaling, cyclin D1, post-transcriptional regulation, therapeutic target
MeSH terms: Endometriosis, Female, Gene Expression Regulation, Multigene Family, Humans, Molecular Sequence Data, Signal Transduction, Oligonucleotide Array Sequence Analysis, Gene Expression Profiling, MicroRNAs, JNK Mitogen-Activated Protein Kinases

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