Laguë Marie-Noëlle, Paquet Marilène, Fan Heng-Yu, Kaartinen M Johanna, Chu Simon, Jamin Soazik P, Behringer Richard R, Fuller Peter J, Mitchell Andrew, Doré Monique, Huneault Louis M, Richards Joanne S, Boerboom Derek
Centre de Recherche en Reproduction Animale, Faculté de Médecine Vétérinaire, Université de Montréal, Saint-Hyacinthe, Québec J2S 7C6, Canada.
Carcinogenesis. 2008 Nov;29(11):2062-72. doi: 10.1093/carcin/bgn186. Epub 2008 Aug 6.
The mechanisms of granulosa cell tumor (GCT) development may involve the dysregulation of signaling pathways downstream of follicle-stimulating hormone, including the phosphoinosite-3 kinase (PI3K)/AKT pathway. To test this hypothesis, a genetically engineered mouse model was created to derepress the PI3K/AKT pathway in granulosa cells by conditional targeting of the PI3K antagonist gene Pten (Pten(flox/flox);Amhr2(cre/+)). The majority of Pten(flox/flox);Amhr2(cre/+) mice featured no ovarian anomalies, but occasionally ( approximately 7%) developed aggressive, anaplastic GCT with pulmonary metastases. The expression of the PI3K/AKT downstream effector FOXO1 was abrogated in Pten(flox/flox);Amhr2(cre/+) GCT, indicating a mechanism by which GCT cells may increase proliferation and evade apoptosis. To relate these findings to spontaneously occurring GCT, analyses of PTEN and phospho-AKT expression were performed on human and equine tumors. Although PTEN loss was not detected, many GCT (2/5 human, 7/17 equine) featured abnormal nuclear or perinuclear localization of phospho-AKT, suggestive of altered PI3K/AKT activity. As inappropriate activation of WNT/CTNNB1 signaling causes late-onset GCT development and cross talk between the PI3K/AKT and WNT/CTNNB1 pathways has been reported, we tested whether these pathways could synergize in GCT. Activation of both the PI3K/AKT and WNT/CTNNB1 pathways in the granulosa cells of a mouse model (Pten(flox/flox);Ctnnb1(flox(ex3)/+);Amhr2(cre/+)) resulted in the development of GCT similar to those observed in Pten(flox/flox);Amhr2(cre/+) mice, but with 100% penetrance, perinatal onset, extremely rapid growth and the ability to spread by seeding into the abdominal cavity. These data indicate a synergistic effect of dysregulated PI3K/AKT and WNT/CTNNB1 signaling in the development and progression of GCT and provide the first animal models for metastatic GCT.
颗粒细胞瘤(GCT)的发生机制可能涉及促卵泡激素下游信号通路的失调,包括磷酸肌醇-3激酶(PI3K)/AKT通路。为了验证这一假设,构建了一种基因工程小鼠模型,通过条件性靶向PI3K拮抗剂基因Pten(Pten(flox/flox);Amhr2(cre/+))来解除颗粒细胞中PI3K/AKT通路的抑制。大多数Pten(flox/flox);Amhr2(cre/+)小鼠没有卵巢异常,但偶尔(约7%)会发生侵袭性、间变性GCT并伴有肺转移。PI3K/AKT下游效应因子FOXO1在Pten(flox/flox);Amhr2(cre/+) GCT中的表达被消除,这表明GCT细胞可能通过这种机制增加增殖并逃避凋亡。为了将这些发现与自发发生的GCT联系起来,对人和马的肿瘤进行了PTEN和磷酸化AKT表达分析。虽然未检测到PTEN缺失,但许多GCT(2/5人,7/17马)的磷酸化AKT呈现异常的核内或核周定位,提示PI3K/AKT活性改变。由于WNT/CTNNB1信号通路的不适当激活会导致迟发性GCT发生,且已有报道PI3K/AKT与WNT/CTNNB1通路之间存在相互作用,我们测试了这些通路在GCT中是否能协同作用。在小鼠模型(Pten(flox/flox);Ctnnb1(flox(ex3)/+);Amhr2(cre/+))的颗粒细胞中同时激活PI3K/AKT和WNT/CTNNB1通路,导致GCT的发生,类似于在Pten(flox/flox);Amhr2(cre/+)小鼠中观察到的情况,但具有100%的外显率、围产期发病、极快的生长速度以及通过植入腹腔进行扩散的能力。这些数据表明PI3K/AKT和WNT/CTNNB1信号通路失调在GCT的发生和发展中具有协同作用,并提供了首个转移性GCT动物模型。