C-Met activation leads to the establishment of a TGF?-receptor regulatory network in bladder cancer progression.

ABSTRACT: Treatment of muscle-invasive bladder cancer remains a major clinical challenge. Aberrant HGF/c-MET upregulation and activation is frequently observed in bladder cancer correlating with cancer progression and invasion. However, the mechanisms underlying HGF/c-MET-mediated invasion in bladder cancer remains unknown. As part of a negative feedback loop SMAD7 binds to SMURF2 targeting the TGF? receptor for degradation. Under these conditions, SMAD7 acts as a SMURF2 agonist by disrupting the intramolecular interactions within SMURF2. We demonstrate that HGF stimulates TGF? signalling through c-SRC-mediated phosphorylation of SMURF2 resulting in loss of SMAD7 binding and enhanced SMURF2 C2-HECT interaction, inhibiting SMURF2 and enhancing TGF? receptor stabilisation. This upregulation of the TGF? pathway by HGF leads to TGF?-mediated EMT and invasion. In vivo we show that TGF? receptor inhibition prevents bladder cancer invasion. Furthermore, we make a rationale for the use of combinatorial TGF? and MEK inhibitors for treatment of high-grade non-muscle-invasive bladder cancers.

SUBMITTER: Sim WJ 

PROVIDER: S-EPMC6761206 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature