Endometrial expression of estrogen receptor β and its splice variants in patients with and without endometriosis

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This study examined the expression of four main ERβ transcript isoforms in human endometrial tissue from women with and without endometriosis, finding altered ERα/ERβ1 ratios in proliferative endometrium of endometriosis patients.

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This study examined estrogen receptor β (ERβ) by assessing four main ERβ transcript isoforms (β1, β2, β4, β5) and ERα transcripts in native human endometrial tissue from prospectively collected women with endometriosis and women without endometriosis, stratified by menstrual cycle phase using RT-PCR. ERα, ERβ1, ERβ2, and ERβ5 transcripts were detected in both proliferative and secretory phases, with no relevant cycle-dependent change in receptor transcript expression strength. In the proliferative phase, women without endometriosis had a significantly higher ERα/ERβ1 ratio than patients with endometriosis, and ERα mRNA was consistently higher than ERβ isoform transcript levels. The study included a small sample size and does not establish causality, despite suggesting ERβ1 may be involved in endometriosis pathogenesis, and it does not quantify other ERβ splice variants beyond the four assayed. This paper is centrally about endometriosis — it compares endometrial ERβ splice variant expression and the ERα/ERβ1 ratio between patients with and without endometriosis.

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Abstract

Background The role of estrogen receptor beta (ERβ) in pathogenesis of endometriosis remains to be elucidated. In this study, we have examined the expression of the four main ERβ transcript isoforms in human endometrial tissue in women with or without endometriosis.

Methods

Total RNA was isolated from native endometrial tissue and transcript levels of ERα, β1, β2, β4, β5 were analyzed by means of RT-PCR. We compared the results with regard to menstrual cycle phase as well as to presence or absence of endometriosis. We prospectively harvested the endometrium of ten women without endometriosis (five for each cycle phase) and eight patients with endometriosis (five in the proliferative phase, three in the secretory phase).

Results

ERα, β1, β2, and β5 transcripts were detected in both cycle phases. During the proliferative phase, healthy women had a significantly higher ERα/ERβ1-ratio than patients with endometriosis. Irrespective of the cycle phase, ERα-mRNA level was significantly higher than transcript levels of ERβ isoforms.

Conclusions

ERα, β1, β2, and β5 are expressed in human endometrium. The individual receptors differed in terms of expression strength but there was no relevant change during the cycle. The decreased ERα/ERβ1-ratio in proliferative endometrium of endometriosis patients suggest that ERβ1 might be involved in the pathogenesis of endometriosis. Further studies should be undertaken to substantiate the role of ERβ in endometrial pathology. Similar content being viewed by others

References

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Condition tags

endometriosis

MeSH descriptors

Endometriosis Endometrium Estrogen Receptor beta Adult Endometriosis Endometrium Estrogen Receptor beta Estrogen Receptor beta Female Humans Menstrual Cycle Menstrual Cycle Prospective Studies Protein Isoforms Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger RNA, Messenger

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