Dataset Information


H2O2 induces nuclear transport of the receptor tyrosine kinase c-MET in breast cancer cells via a membrane-bound retrograde trafficking mechanism.

ABSTRACT: Reactive oxygen species (ROS) are cellular by-products produced from metabolism and also anticancer agents, such as ionizing irradiation and chemotherapy drugs. The ROS H2O2 has high rates of production in cancer cells because of their rapid proliferation. ROS oxidize DNA, protein, and lipids, causing oxidative stress in cancer cells and making them vulnerable to other stresses. Therefore, cancer cell survival relies on maintaining ROS-induced stress at tolerable levels. Hepatocyte growth factor receptor (c-MET) is a receptor tyrosine kinase overexpressed in malignant cancer types, including breast cancer. Full-length c-MET triggers a signal transduction cascade from the plasma membrane that, through downstream signaling proteins, up-regulates cell proliferation and migration. Recently, c-MET was shown to interact and phosphorylate poly(ADP-ribose) polymerase 1 in the nucleus and to induce poly(ADP-ribose) polymerase inhibitor resistance. However, it remains unclear how c-MET moves from the cell membrane to the nucleus. Here, we demonstrate that H2O2 induces retrograde transport of membrane-associated full-length c-MET into the nucleus of human MCF10A and MCF12A or primary breast cancer cells. We further show that knocking down either coatomer protein complex subunit ?1 (COPG1) or Sec61 translocon ? subunit (SEC61?) attenuates the accumulation of full-length nuclear c-MET. However, a c-MET kinase inhibitor did not block nuclear c-MET transport. Moreover, nuclear c-MET interacted with KU proteins in breast cancer cells, suggesting a role of full-length nuclear c-MET in ROS-induced DNA damage repair. We conclude that a membrane-bound retrograde vesicle transport mechanism facilitates membrane-to-nucleus transport of c-MET in breast cancer cells.


PROVIDER: S-EPMC6544865 | BioStudies | 2019-01-01


REPOSITORIES: biostudies

Similar Datasets

1000-01-01 | S-EPMC2992305 | BioStudies
1000-01-01 | S-EPMC3351284 | BioStudies
2017-01-01 | S-EPMC5661625 | BioStudies
2017-01-01 | S-EPMC5575308 | BioStudies
1000-01-01 | S-EPMC3982987 | BioStudies
2019-01-01 | S-EPMC6760253 | BioStudies
2017-01-01 | S-EPMC5672155 | BioStudies
1000-01-01 | S-EPMC5946456 | BioStudies
1000-01-01 | S-EPMC3143642 | BioStudies
2015-01-01 | S-EPMC4579783 | BioStudies