Transcriptional regulation of the p73 gene by Nrf-2 and promoter CpG methylation in human breast cancer

• Published in: Oncotarget Vol. 5; no. 16; pp. 6909 - 6922
• Main Authors: Lai, Jing, Nie, Weiwei, Zhang, Wenwen, Wang, Yucai, Xie, Ruilian, Wang, Yanru, Gu, Jun, Xu, Jing, Song, Wei, Yang, Fang, Huang, Guichun, Cao, Peng, Guan, Xiaoxiang
• Format: Journal Article
• Language: English
• Published: United States Impact Journals LLC 30.08.2014
• Subjects: Animals; Apoptosis - genetics; Breast Neoplasms - genetics; Breast Neoplasms - pathology; Cell Proliferation - genetics; CpG Islands; DNA Methylation; DNA-Binding Proteins - genetics; Female; Gene Expression Regulation, Neoplastic; Genes, Tumor Suppressor; Humans; MCF-7 Cells; Mice; Mice, Inbred C57BL; Mice, Knockout; NF-E2-Related Factor 2 - genetics; Nuclear Proteins - genetics; Promoter Regions, Genetic; Research Paper; Transfection; Tumor Protein p73; Tumor Suppressor Proteins - genetics
• ISSN: 1949-2553; 1949-2553
• DOI: 10.18632/oncotarget.2230

To understand the transcriptional regulation of p73 by promoter methylation and Nrf-2 in breast carcinogenesis, ChIP assay indicated that Nrf-2 can bind to both promoters and can activate the transcription of TAp73 and ΔNp73 in MCF-7 cell line, knockdown of Nrf-2 gene resulted in an abrogation of TAp73 and ΔNp73 expression in the cells transfected with sh-Nrf-2 as well as Nrf-2 knock out mouse model. However, we found Nrf-2 induced ΔNp73 expression was abolished with 5-aza-dC treatment, thus lead to a down-regulated ΔNp73 and an up-regulated TAp73 expression in breast cancer cells lines. Consistent with this model, we detected decreased TAp73 and increased ΔNp73 expression in breast cancer tissue, along with increased TAp73 but decreased ΔNp73 expression in corresponding surrounding noncancerous tissues (NCTs) in a breast cancer tissue assay. A significant inverse correlation was found between TAp73 and ΔNp73 expression in the above tissue-array (P = 0.047) and validated in another set consisting of 128 breast cancer tumor tissue (P = 0.034). Taken together, our findings suggest that Nrf-2 and promoter methylation cooperatively govern the transcriptional regulation of p73, and unbalanced expression of TAp73 and ΔNp73 expression plays a critical role in breast cancer development.