Nrf2 promotes breast cancer cell migration via up-regulation of G6PD/HIF-1α/Notch1 axis.
Hong-Sheng ZhangZhong-Guo ZhangGuang-Yuan DuHong-Liang SunHui-Yun LiuZhen ZhouXiao-Meng GouXi-Hao WuXiao-Ying YuYing-Hui HuangPublished in: Journal of cellular and molecular medicine (2019)
Abnormal metabolism of tumour cells is closely related to the occurrence and development of breast cancer, during which the expression of NF-E2-related factor 2 (Nrf2) is of great significance. Metastatic breast cancer is one of the most common causes of cancer death worldwide; however, the molecular mechanism underlying breast cancer metastasis remains unknown. In this study, we found that the overexpression of Nrf2 promoted proliferation and migration of breast cancers cells. Inhibition of Nrf2 and overexpression of Kelch-like ECH-associated protein 1 (Keap1) reduced the expression of glucose-6-phosphate dehydrogenase (G6PD) and transketolase of pentose phosphate pathway, and overexpression of Nrf2 and knockdown of Keap1 had opposite effects. Our results further showed that the overexpression of Nrf2 promoted the expression of G6PD and Hypoxia-inducing factor 1α (HIF-1α) in MCF-7 and MDA-MB-231 cells. Overexpression of Nrf2 up-regulated the expression of Notch1 via G6PD/HIF-1α pathway. Notch signalling pathway affected the proliferation of breast cancer by affecting its downstream gene HES-1, and regulated the migration of breast cancer cells by affecting the expression of EMT pathway. The results suggest that Nrf2 is a potential molecular target for the treatment of breast cancer and targeting Notch1 signalling pathway may provide a promising strategy for the treatment of Nrf2-driven breast cancer metastasis.
Keyphrases
- oxidative stress
- induced apoptosis
- poor prognosis
- cell proliferation
- breast cancer cells
- transcription factor
- cell migration
- binding protein
- signaling pathway
- endothelial cells
- long non coding rna
- squamous cell carcinoma
- risk assessment
- gene expression
- epithelial mesenchymal transition
- immune response
- small molecule
- skeletal muscle
- endoplasmic reticulum stress
- genome wide
- adipose tissue
- replacement therapy
- insulin resistance
- young adults
- cancer therapy
- drug induced
- blood glucose
- squamous cell
- glycemic control