Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston Texas 77030, USA.
Endocrinology. 2012 Apr;153(4):1638-48. doi: 10.1210/en.2011-2131. Epub 2012 Mar 6.
Loss of Pten in the Kras(G12D);Amhr2-Cre mutant mice leads to the transformation of ovarian surface epithelial (OSE) cells and rapid development of low-grade, invasive serous adenocarcinomas. Tumors occur with 100% penetrance and express elevated levels of wild-type tumor repressor protein 53 (TRP53). To test the functions of TRP53 in the Pten;Kras (Trp53+) mice, we disrupted the Trp53 gene yielding Pten;Kras(Trp53-) mice. By comparing morphology and gene expression profiles in the Trp53+ and Trp53- OSE cells from these mice, we document that wild-type TRP53 acts as a major promoter of OSE cell survival and differentiation: cells lacking Trp53 are transformed yet are less adherent, migratory, and invasive and exhibit a gene expression profile more like normal OSE cells. These results provide a new paradigm: wild-type TRP53 does not preferentially induce apoptotic or senescent related genes in the Pten;Kras(Trp53+) cancer cells but rather increases genes regulating DNA repair, cell cycle progression, and proliferation and decreases putative tumor suppressor genes. However, if TRP53 activity is forced higher by exposure to nutlin-3a (a mouse double minute-2 antagonist), TRP53 suppresses DNA repair genes and induces the expression of genes that control cell cycle arrest and apoptosis. Thus, in the Pten;Kras(Trp53+) mutant mouse OSE cells and likely in human TP53+ low-grade ovarian cancer cells, wild-type TRP53 controls global molecular changes that are dependent on its activation status. These results suggest that activation of TP53 may provide a promising new therapy for managing low-grade ovarian cancer and other cancers in humans in which wild-type TP53 is expressed.
Pten 缺失和 Kras(G12D);Amhr2-Cre 突变型小鼠导致卵巢表面上皮(OSE)细胞的转化和低级别、侵袭性浆液性腺癌的快速发展。肿瘤的发生率为 100%,并表达高水平的野生型肿瘤抑制蛋白 53(TRP53)。为了测试 TRP53 在 Pten;Kras(Trp53+)小鼠中的功能,我们敲除了 Trp53 基因,得到了 Pten;Kras(Trp53-)小鼠。通过比较这些小鼠中 Trp53+和 Trp53-OSE 细胞的形态和基因表达谱,我们证明野生型 TRP53 作为 OSE 细胞存活和分化的主要促进因子:缺乏 Trp53 的细胞发生转化,但细胞黏附性、迁移性和侵袭性降低,基因表达谱更类似于正常 OSE 细胞。这些结果提供了一个新的范例:野生型 TRP53 不会优先在 Pten;Kras(Trp53+)癌细胞中诱导凋亡或衰老相关基因,而是增加调节 DNA 修复、细胞周期进程和增殖的基因,并减少潜在的肿瘤抑制基因。然而,如果 TRP53 活性因暴露于 nutlin-3a(一种小鼠双微体-2 拮抗剂)而被迫升高,TRP53 会抑制 DNA 修复基因,并诱导控制细胞周期停滞和细胞凋亡的基因表达。因此,在 Pten;Kras(Trp53+)突变型小鼠 OSE 细胞中,很可能在人类 TP53+低级别卵巢癌中,野生型 TRP53 控制着依赖其激活状态的全局分子变化。这些结果表明,TP53 的激活可能为管理低级别卵巢癌和其他在人类中表达野生型 TP53 的癌症提供一种有前途的新疗法。