Caveolin-1 is involved in radiation-induced ERBB2 nuclear transport in breast cancer cells.
10.1007/s11596-012-1053-z
- Author:
Yu ZHANG
1
;
Shiying YU
;
Liang ZHUANG
;
Zu'an ZHENG
;
Tengfei CHAO
;
Qiang FU
Author Information
1. Cancer Centre, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China. roalfan@163.com
- Publication Type:Journal Article
- MeSH:
Active Transport, Cell Nucleus;
physiology;
Breast Neoplasms;
metabolism;
physiopathology;
Caveolin 1;
metabolism;
Cell Line, Tumor;
Female;
Humans;
Protein Transport;
physiology;
Radiation;
Receptor, ErbB-2;
metabolism
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2012;32(6):888-892
- CountryChina
- Language:English
-
Abstract:
This study examined the radiation-induced ERBB2 nuclear transport in the BT474 breast cancer cell line and the relationship between caveolin-1 and radiation-induced ERBB2 nuclear transport. The BT474 cells were treated with herceptin (200 nmol/L), PP2 (a caveolin-1 inhibitor, 100 nmol/L) and irradiation combined or alone. Confocal microscopy was used to observe the nuclear import of ERBB2 and caveolin-1 after irradiation. Western blotting was employed to detect the expression of ERBB2, caveolin-1 and DNA-PKcs after irradiation, and immunoprecipitation to identify the ERBB2 and caveolin-1 complex before perinuclear ERBB2 localization. Confocal microscopy showed the transport of ERBB2 and caveolin-1 from the cell membrane to the nucleus 15 min after irradiation and the proteins accumulated at the perinuclear region within 45 min. Western blotting revealed that the expression levels of ERBB2, caveolin-1 and DNA-PKcs were increased after irradiation and reached a peak 45 min later. Both herceptin and PP2 treatments were found to decrease ERBB2 expression. An immune complex composed of ERBB2 and caveolin-1 was found in the herceptin group after irradiation. It was concluded that after irradiation, ERBB2 may be transported from the cell membrane to the nucleus and activate DNA-PKcs to trigger DNA double-strand break (DSB) repair; caveolin-1 may participate in this process. Treatments involving the downregulation of caveolin-1 may increase the radiosensitization of breast cancer cells.
