Washington State University, Spokane, 99164, USA.
Cell Mol Biol Lett. 2010 Jun;15(2):272-95. doi: 10.2478/s11658-010-0007-3. Epub 2010 Feb 25.
Id1 (inhibitor of differentiation 1) is a member of the bHLH protein family. Consistent with its role in promoting proliferation and inhibiting differentiation, Id1 expression is low or negligible in normal prostate epithelial cells but is high in prostate cancer. Ectopic expression of Id1 in normal prostate epithelial cells could therefore provide a model for understanding early events involved in initiation of prostate cancer. Over-expression of Id1 immortalized but did not transform ventral prostate epithelial cells (Id1-RPE). Immortalization was associated with decreased Cdkn2a, Cdkn1a, androgen receptor and increased Tert expression. Gene expression profiling over successive doublings was used to identify transcriptomic changes involved during immortalization (Tieg, Jun, alpha actin, Klf10, Id2) and in maintaining the immortalized phenotype (Igfbp3, Igfbp5, Mmp2, Tgfb3). Network analysis indicated that Id1 promotes cancer/tumor morphology, cell cycle and epithelial to mesenchymal transition by influencing AP1, tnf, tgfbeta, PdgfBB and estradiol pathways. During immortalization, the expression of majority of differentially expressed genes reduced over progressive doublings suggesting a decline in transcriptional regulatory mechanisms. The associated molecular/gene expression profile of Id1-RPE cells provides an opportunity to understand the molecular pathways associated with prostate epithelial cell survival and proliferation.
Id1(分化抑制因子 1)是 bHLH 蛋白家族的一员。Id1 在促进增殖和抑制分化方面发挥作用,因此在正常前列腺上皮细胞中表达水平较低或可忽略不计,但在前列腺癌中表达水平较高。在正常前列腺上皮细胞中异位表达 Id1 可以为理解前列腺癌起始涉及的早期事件提供模型。Id1 的过表达可使前列腺上皮细胞永生化,但不能转化(Id1-RPE)。永生化与 Cdkn2a、Cdkn1a、雄激素受体的表达降低和 Tert 的表达增加有关。通过对连续倍增的基因表达谱进行分析,鉴定出与永生化相关的转录组变化(Tieg、Jun、α肌动蛋白、Klf10、Id2)和维持永生化表型相关的变化(Igfbp3、Igfbp5、Mmp2、Tgfb3)。网络分析表明,Id1 通过影响 AP1、tnf、tgfbeta、PdgfBB 和雌二醇途径促进癌症/肿瘤形态、细胞周期和上皮间质转化。在永生化过程中,随着连续倍增,大多数差异表达基因的表达减少,这表明转录调控机制下降。Id1-RPE 细胞的相关分子/基因表达谱为理解与前列腺上皮细胞存活和增殖相关的分子途径提供了机会。