Lanza Denise G, Dawson Emily P, Rao Priya, Heaney Jason D
a Department of Molecular and Human Genetics , Baylor College of Medicine , Houston , TX , USA.
b Department of Pathology , MD Anderson Cancer Center, The University of Texas , Houston , TX , USA.
Cell Cycle. 2016;15(7):919-30. doi: 10.1080/15384101.2016.1149272. Epub 2016 Feb 22.
Testicular teratomas result from anomalies in embryonic germ cell development. In the 129 family of inbred mouse strains, teratomas arise during the same developmental period that male germ cells normally enter G1/G0 mitotic arrest and female germ cells initiate meiosis (the mitotic:meiotic switch). Dysregulation of this switch associates with teratoma susceptibility and involves three germ cell developmental abnormalities seemingly critical for tumor initiation: delayed G1/G0 mitotic arrest, retention of pluripotency, and misexpression of genes normally restricted to embryonic female and adult male germ cells. One misexpressed gene, cyclin D1 (Ccnd1), is a known regulator of cell cycle progression and an oncogene in many tissues. Here, we investigated whether Ccnd1 misexpression in embryonic germ cells is a determinant of teratoma susceptibility in mice. We found that CCND1 localizes to teratoma-susceptible germ cells that fail to enter G1/G0 arrest during the mitotic:meiotic switch and is the only D-type cyclin misexpressed during this critical developmental time frame. We discovered that Ccnd1 deficiency in teratoma-susceptible mice significantly reduced teratoma incidence and suppressed the germ cell proliferation and pluripotency abnormalities associated with tumor initiation. Importantly, Ccnd1 expression was dispensable for somatic cell development and male germ cell specification and maturation in tumor-susceptible mice, implying that the mechanisms by which Ccnd1 deficiency reduced teratoma incidence were germ cell autonomous and specific to tumorigenesis. We conclude that misexpression of Ccnd1 in male germ cells is a key component of a larger pro-proliferative program that disrupts the mitotic:meiotic switch and predisposes 129 inbred mice to testicular teratocarcinogenesis.
睾丸畸胎瘤是由胚胎生殖细胞发育异常引起的。在近交系小鼠129家族中,畸胎瘤出现在雄性生殖细胞正常进入G1/G0有丝分裂停滞且雌性生殖细胞开始减数分裂(有丝分裂:减数分裂转换期)的同一发育时期。这种转换的失调与畸胎瘤易感性相关,并且涉及三个对肿瘤起始似乎至关重要的生殖细胞发育异常:延迟的G1/G0有丝分裂停滞、多能性的保留以及通常仅限于胚胎期雌性和成年雄性生殖细胞的基因的错误表达。一个错误表达的基因,细胞周期蛋白D1(Ccnd1),是细胞周期进程的已知调节因子,并且在许多组织中是一种癌基因。在这里,我们研究了胚胎生殖细胞中Ccnd1的错误表达是否是小鼠畸胎瘤易感性的决定因素。我们发现CCND1定位于在有丝分裂:减数分裂转换期未能进入G1/G0停滞的易患畸胎瘤的生殖细胞,并且是在这个关键发育时间框架内唯一错误表达的D型细胞周期蛋白。我们发现,易患畸胎瘤的小鼠中Ccnd1的缺失显著降低了畸胎瘤的发生率,并抑制了与肿瘤起始相关的生殖细胞增殖和多能性异常。重要的是,在易患肿瘤的小鼠中,Ccnd1的表达对于体细胞发育以及雄性生殖细胞的特化和成熟是可有可无的,这意味着Ccnd1缺失降低畸胎瘤发生率的机制是生殖细胞自主的且对肿瘤发生具有特异性。我们得出结论,雄性生殖细胞中Ccnd1的错误表达是一个更大的促进增殖程序的关键组成部分,该程序破坏了有丝分裂:减数分裂转换,并使129近交系小鼠易患睾丸畸胎癌发生。