Shepherd T, Hassell J A
Institute for Molecular Biology and Biotechnology, McMaster University, Hamilton, Ontario, Canada.
J Mammary Gland Biol Neoplasia. 2001 Jan;6(1):129-40. doi: 10.1023/a:1009576801226.
PEA3 is the founding member of a subfamily of closely related ets genes that includes ER81 and ERM. PEA3 is expressed in the epithelial cells of mammary buds at the time that these first appear during mouse embryogenesis, and it is differentially expressed during postnatal mammary gland development. PEA3 expression is highest at the onset of puberty and during early pregnancy, times of extensive epithelial outgrowth and branching. PEA3 is expressed in undifferentiated epithelial cap cells of terminal end buds, and in differentiated myoepithelial cells of ducts and alveoli. Loss-of-function mutations in the PEA3 gene compromise mammary ductal branching at the onset of puberty and early during pregnancy. PEA3 is overexpressed in the vast majority of human breast tumors and in nearly all of the HER2-positive subclass of such tumors. PEA3 is similarly overexpressed in transgenic mouse models of this malignancy. Expression of dominant-negative PEA3 in the mouse mammary gland of MMTV-HER2 transgenic mice dramatically delays the onset and reduces the incidence of mammary tumors. Hence PEA3 and/or its close relatives play key regulatory roles in both mammary gland development and oncogenesis.
PEA3是一个紧密相关的ets基因亚家族的创始成员,该亚家族包括ER81和ERM。在小鼠胚胎发育过程中,乳腺芽首次出现时,PEA3就在其上皮细胞中表达,并且在出生后乳腺发育过程中差异表达。PEA3在青春期开始时和妊娠早期表达最高,这两个时期是上皮大量生长和分支的时期。PEA3在终末芽的未分化上皮帽细胞以及导管和腺泡的分化肌上皮细胞中表达。PEA3基因的功能缺失突变会在青春期开始时和妊娠早期损害乳腺导管分支。PEA3在绝大多数人类乳腺肿瘤以及几乎所有此类肿瘤的HER2阳性亚类中过表达。在这种恶性肿瘤的转基因小鼠模型中,PEA3同样过表达。在MMTV-HER2转基因小鼠的乳腺中表达显性负性PEA3会显著延迟乳腺肿瘤的发生并降低其发生率。因此,PEA3和/或其近亲在乳腺发育和肿瘤发生中都起着关键的调节作用。