Rigosertib-Activated JNK1/2 Eliminate Tumor Cells through p66Shc Activation
Rigosertib, via reactive oxygen species (ROS), stimulates cJun N-terminal kinases 1/2 (JNK1/2), which inactivate RAS/RAF signaling and thereby inhibit growth and survival of tumor cells. JNK1/2 are not only regulated by ROS—they in turn can also control ROS production. The prooxidant and cell death...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-05-01
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Series: | Biology |
Subjects: | |
Online Access: | https://www.mdpi.com/2079-7737/9/5/99 |