PI3K/AKT activation induces PTEN ubiquitination and destabilization accelerating tumourigenesis

Author:

Lee Min-Sik,Jeong Man-Hyung,Lee Hyun-Woo,Han Hyun-Ji,Ko Aram,Hewitt Stephen M.,Kim Jae-Hoon,Chun Kyung-Hee,Chung Joon-Yong,Lee Cheolju,Cho Hanbyoul,Song Jaewhan

Abstract

AbstractThe activity of the phosphatase and tensin homologue (PTEN) is known to be suppressed via post-translational modification. However, the mechanism and physiological significance by which post-translational modifications lead to PTEN suppression remain unclear. Here we demonstrate that PTEN destabilization is induced by EGFR- or oncogenic PI3K mutation-mediated AKT activation in cervical cancer. EGFR/PI3K/AKT-mediated ubiquitination and degradation of PTEN are dependent on the MKRN1 E3 ligase. These processes require the stabilization of MKRN1 via AKT-mediated phosphorylation. In cervical cancer patients with high levels of pAKT and MKRN1 expression, PTEN protein levels are low and correlate with a low 5-year survival rate. Taken together, our results demonstrate that PI3K/AKT signals enforce positive-feedback regulation by suppressing PTEN function.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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