Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

APC2 is critical for ovarian WNT signalling control, fertility and tumour suppression

Mohamed, Noha-Ehssan, Hay, Trevor, Reed, Karen R., Smalley, Matthew J. and Clarke, Alan R. 2019. APC2 is critical for ovarian WNT signalling control, fertility and tumour suppression. BMC Cancer 19 , 677. 10.1186/s12885-019-5867-y

[img]
Preview
Image (JPEG) (Fig 1) - Supplemental Material
Download (942kB) | Preview
[img]
Preview
Image (JPEG) (Sup Fig 1) - Supplemental Material
Download (1MB) | Preview
[img]
Preview
Image (JPEG) (Sup Fig 2) - Supplemental Material
Download (1MB) | Preview
[img]
Preview
Image (JPEG) (Sup Fig 3) - Supplemental Material
Download (745kB) | Preview
[img]
Preview
Image (JPEG) (Sup Fig 4) - Supplemental Material
Download (1MB) | Preview
[img]
Preview
Image (JPEG) (Fig 5) - Supplemental Material
Download (492kB) | Preview
[img]
Preview
Image (JPEG) (Fig 6) - Supplemental Material
Download (1MB) | Preview
[img]
Preview
PDF (Fig Legends) - Supplemental Material
Download (53kB) | Preview
[img]
Preview
PDF - Published Version
Available under License Creative Commons Attribution.

Download (4MB) | Preview

Abstract

Background Canonical WNT signalling plays a critical role in the regulation of ovarian development; mis-regulation of this key pathway in the adult ovary is associated with subfertility and tumourigenesis. The roles of Adenomatous polyposis coli 2 (APC2), a little-studied WNT signalling pathway regulator, in ovarian homeostasis, fertility and tumourigenesis have not previously been explored. Here, we demonstrate essential roles of APC2 in regulating ovarian WNT signalling and ovarian homeostasis. Methods A detailed analysis of ovarian histology, gene expression, ovulation and hormone levels was carried out in 10 week old and in aged constitutive APC2-knockout (Apc2−/−) mice (mixed background). Statistical significance for qRT-PCR data was determined from 95% confidence intervals. Significance testing was performed using 2-tailed Student’s t-test, when 2 experimental cohorts were compared. When more were compared, ANOVA test was used, followed by a post-hoc test (LSD or Games-Howell). P-values of < 0.05 were considered statistically significant. Results APC2-deficiency resulted in activation of ovarian WNT signalling and sub-fertility driven by intra-ovarian defects. Follicular growth was perturbed, resulting in a reduced rate of ovulation and corpora lutea formation, which could not be rescued by administration of gonadotrophins. Defects in steroidogenesis and follicular vascularity contributed to the subfertility phenotype. Tumour incidence was assessed in aged APC2-deficient mice, which also carried a hypomorphic Apc allele. APC2-deficiency in these mice resulted in predisposition to granulosa cell tumour (GCT) formation, accompanied by acute tumour-associated WNT-signalling activation and a histologic pattern and molecular signature seen in human adult GCTs. Conclusions Our work adds APC2 to the growing list of WNT-signalling members that regulate ovarian homeostasis, fertility and suppress GCT formation. Importantly, given that the APC2-deficient mouse develops tumours that recapitulate the molecular signature and histological features of human adult GCTs, this mouse has excellent potential as a pre-clinical model to study ovarian subfertility and transitioning to GCT, tumour biology and for therapeutic testing.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Biosciences
European Cancer Stem Cell Research Institute (ECSCRI)
Publisher: BMC
ISSN: 1471-2407
Date of First Compliant Deposit: 24 June 2019
Date of Acceptance: 23 June 2019
Last Modified: 19 Jul 2019 13:04
URI: http://orca-mwe.cf.ac.uk/id/eprint/123704

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics