Park Joon T, Shih Ie-Ming, Wang Tian-Li
Department of Pathology, Pathobiology Graduate Program, Johns Hopkins Medical Institutions, Baltimore, Maryland 21231, USA.
Cancer Res. 2008 Nov 1;68(21):8852-60. doi: 10.1158/0008-5472.CAN-08-0517.
Notch3 gene amplification has recently been identified in ovarian cancer but the Notch3 effectors that are involved in the development of ovarian cancer remain elusive. In this study, we have identified Pbx1, a proto-oncogene in hematopoietic malignancy, as a Notch3 target gene. Pbx1 expression is transcriptionally regulated by Notch3 activation, and Notch3/CSL protein complex directly binds to the Pbx1 promoter segment harboring the CSL-binding sequence. The growth-inhibitory effect of gamma-secretase inhibitor could be partially reversed by ectopic Pbx1 expression. Furthermore, functional studies by Pbx1 short hairpin RNA knockdown show that Pbx1 is essential for cell proliferation and tumorigenicity. Taken together, the above findings indicate that Pbx1 is a direct Notch3-regulated gene that mediates the survival signal of Notch3 in ovarian cancer.
Notch3基因扩增最近在卵巢癌中被发现,但参与卵巢癌发生发展的Notch3效应因子仍不清楚。在本研究中,我们确定了造血系统恶性肿瘤中的原癌基因Pbx1为Notch3靶基因。Pbx1的表达受Notch3激活的转录调控,Notch3/CSL蛋白复合物直接结合到含有CSL结合序列的Pbx1启动子片段上。γ-分泌酶抑制剂的生长抑制作用可通过异位表达Pbx1而部分逆转。此外,通过Pbx1短发夹RNA敲低进行的功能研究表明,Pbx1对细胞增殖和致瘤性至关重要。综上所述,上述发现表明Pbx1是一个直接受Notch3调控的基因,介导Notch3在卵巢癌中的生存信号。