Stiles Bangyan, Groszer Matthias, Wang Shunyou, Jiao Jing, Wu Hong
Department of Molecular and Medical Pharmacology, UCLA David Geffen School of Medicine, CHS23-234, Los Angeles, CA 90095, USA.
Dev Biol. 2004 Sep 15;273(2):175-84. doi: 10.1016/j.ydbio.2004.06.008.
Recent studies indicate that certain key molecules that are vital for various developmental processes, such as Wnt, Shh, and Notch, cause cancer when dysregulated. PTEN, a tumor suppressor that antagonizes the PI3 kinase pathway, is the newest one on the list. The biological function of PTEN is evolutionarily conserved from C. elegans to humans, and the PTEN-controlled signaling pathway regulates cellular processes crucial for normal development, including cell proliferation, soma growth, cell death, and cell migration. In this review, we will focus on the function of PTEN in murine development and its role in regulating stem cell self-renewal and proliferation. We will summarize the organomegaly phenotypes associated with Pten tissue-specific deletion and discuss how PTEN controls organ size, a fundamental aspect of development. Last, we will review the role of PTEN in hormone-dependent, adult-onset mammary and prostate gland development.
最近的研究表明,某些对各种发育过程至关重要的关键分子,如Wnt、Shh和Notch,一旦失调就会引发癌症。PTEN是一种拮抗PI3激酶途径的肿瘤抑制因子,是该名单上最新的一个。PTEN的生物学功能从秀丽隐杆线虫到人类在进化上是保守的,并且PTEN控制的信号通路调节对正常发育至关重要的细胞过程,包括细胞增殖、体细胞生长、细胞死亡和细胞迁移。在这篇综述中,我们将重点关注PTEN在小鼠发育中的功能及其在调节干细胞自我更新和增殖中的作用。我们将总结与Pten组织特异性缺失相关的器官肿大表型,并讨论PTEN如何控制器官大小,这是发育的一个基本方面。最后,我们将综述PTEN在激素依赖性、成年期乳腺和前列腺发育中的作用。