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DOI 10.1007/s10815-018-1235-0

Медицинская библиотека · Journal of assisted reproduction and genetics · 2018

Hippo signaling in the ovary and polycystic ovarian syndrome.

Maas Kristi, Mirabal Sheyla, Penzias Alan, Sweetnam Paul M, Eggan Kevin C, Sakkas Denny

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Аннотация

PURPOSE: To provide a commentary on our understanding of the role that the Hippo signaling pathway may play in patients with polycystic ovarian syndrome (PCOS) and how this understanding may impact the diagnosis of PCOS.

METHODS

We assessed publications discussing the role of the Hippo signaling pathway in the ovary. In particular, we discuss how Hippo signaling disruption after ovarian fragmentation, combined with treating ovarian fragments with phosphatase and tensin homolog (PTEN) inhibitors and phosphoinositide-3-kinase stimulators to augment AKT signaling, has been used in treatment of patients with primary ovarian insufficiency. Furthermore, we discuss our own data on variations in Hippo signaling pathway gene expression in cumulus cells isolated from women undergoing IVF with a previous diagnosis of PCOS.

RESULTS AND

CONCLUSIONS

Aberrant Hippo signaling in PCOS patients is likely a contributing mechanism to the multifactorial etiology of the disease. Given the challenge of discerning the underlying etiology of oligo-ovulation in some patients, especially those with normal body mass indices, and the need for customized stimulation protocols for PCOS patients who have an increased risk of over-response and higher percentage of immature oocyte yield, it is important to identify these patients prior to treatment. Hippo gene expression fingerprints could potentially be used to more accurately define patients with PCOS. Additionally, targeting this pathway with pharmacologic agents could lead to non-surgical therapeutic options for PCOS.

Для цитирования: Maas Kristi, Mirabal Sheyla, Penzias Alan, Sweetnam Paul M, Eggan Kevin C, Sakkas Denny. Hippo signaling in the ovary and polycystic ovarian syndrome.. Journal of assisted reproduction and genetics. 2018. DOI: 10.1007/s10815-018-1235-0.

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