Autophagy in Endometriosis: Beta-Catenin Suppressive Role

In: Journal of Minimally Invasive Gynecology · 2020 · vol. 27(7) , pp. S66 · doi:10.1016/j.jmig.2020.08.436 · W3096666394
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In ovarian endometriomas, rectocervical and peritoneal endometriosis, and adenomyosis, autophagy markers were down-regulated while beta-catenin was up-regulated compared with eutopic endometrium, suggesting beta-catenin suppresses autophagy.

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This prospective cohort study evaluated autophagic processes and beta-catenin expression in 120 patients with ovarian, rectocervical, peritoneal endometriosis, and adenomyosis compared to their eutopic endometrium. The researchers found significant down-regulation of autophagy markers LAMP1 and LC3 alongside up-regulation of beta-catenin in all ectopic lesion types relative to the eutopic tissue. Although expression levels did not differ significantly among the various lesion localizations, the data supports an inverse relationship where increased beta-catenin suppresses autophagy, potentially aiding cell survival through apoptosis resistance. This paper is centrally about endometriosis and adenomyosis, specifically investigating the molecular mechanisms involving autophagy suppression and beta-catenin upregulation across these specific gynecological conditions.

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Abstract

Study Objective To evaluate the occurrence of the autophagic process in ovarian endometriomas (OE), rectocervical endometriosis (RE), adenomyosis (A), and peritoneal endometriosis (PE) compared with eutopic endometrium. Design Prospective cohort study, Level II-1. Setting National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Healthcare of the Russian Federation. Patients or Participants We recruited 120 patients with endometriosis and adenomyosis: 47 patients with (OE), 20 patients with (RE), 20 patients with (A), 33 patients with (PE). Interventions All patients had laparoscopic surgery performed in the proliferative non-menstrual phase of their menstrual cycle. Histological analysis was carried out according to a standard procedure. Immuno-histochemical analysis of ectopic and eutopic endometrium samples was carried out using the Tissue-Tek Quick-Ray kit, which allows for the preparation of paraffin blocks with a large number of tissue samples (tissue microarray). Antibodies to LAMP 1 (1:100), LC3 (1:50), bcl-2 (1:50), (Ventana, Roche) were used. Measurements and Main Results In patients with EO, RE, A and PE, we noticed a significant down-regulation of autophagy (LAMP1 and LC3 expression) and up-regulation of beta-catenin expression in ectopic endometrium compared with the eutopic endometrium of affected women (p0.05). This data is consistent with our previous observation made on smaller number of patents, possibly confirming the data.

Conclusion

We hypothesized that there is a relationship between autophagy and wnt/signaling pathway regulation, demonstrating the inverse ratio between beta-catenin and autophagy-marker expression. Based on the results in this study, we can say with increased certainty that increased beta-catenin could suppress autophagy, supporting ectopic endometrium through anoikis and other types of apoptosis. So we can suppose that target-based therapy suppressing the wnt/beta-catenin pathway can activate autophagy in endometriosis and, pending clinical studies, become a part of target-based pre-surgical, intra-operative, an post-operative endometriosis therapy.

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endometriosis

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last seen: 2026-06-10T17:14:06.276822+00:00
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