Cowling Victoria H, D'Cruz Celina M, Chodosh Lewis A, Cole Michael D
Dartmouth Medical School, Norris Cotton Cancer Center, One Medical Center Drive, Lebanon, NH 03756, USA.
Mol Cell Biol. 2007 Jul;27(14):5135-46. doi: 10.1128/MCB.02282-06. Epub 2007 May 7.
c-myc is frequently amplified in breast cancer; however, the mechanism of myc-induced mammary epithelial cell transformation has not been defined. We show that c-Myc induces a profound morphological transformation in human mammary epithelial cells and anchorage-independent growth. c-Myc suppresses the Wnt inhibitors DKK1 and SFRP1, and derepression of DKK1 or SFRP1 reduces Myc-dependent transforming activity. Myc-dependent repression of DKK1 and SFRP1 is accompanied by Wnt target gene activation and endogenous T-cell factor activity. Myc-induced mouse mammary tumors have repressed SFRP1 and increased expression of Wnt target genes. DKK1 and SFRP1 inhibit the transformed phenotype of breast cancer cell lines, and DKK1 inhibits tumor formation. We propose a positive feedback loop for activation of the c-myc and Wnt pathways in breast cancer.
c-myc在乳腺癌中常发生扩增;然而,myc诱导乳腺上皮细胞转化的机制尚未明确。我们发现,c-Myc可诱导人乳腺上皮细胞发生显著的形态学转化及非锚定依赖性生长。c-Myc抑制Wnt抑制剂DKK1和SFRP1,而DKK1或SFRP1的去抑制会降低Myc依赖性转化活性。Myc依赖性抑制DKK1和SFRP1伴随着Wnt靶基因激活和内源性T细胞因子活性。Myc诱导的小鼠乳腺肿瘤中SFRP1受到抑制,Wnt靶基因表达增加。DKK1和SFRP1可抑制乳腺癌细胞系的转化表型,且DKK1可抑制肿瘤形成。我们提出了一个在乳腺癌中激活c-myc和Wnt信号通路的正反馈环。