Identifying critical factors involved in the metastatic progression of hepatocellular carcinoma (HCC) may offer important therapeutic opportunities. Here we report that the pro-apoptotic stress response factor TP53INP1 is often selectively down-regulated in advanced stage IV and metastatic human HCC tumors. Mechanistic investigations revealed that TP53INP1 down-regulation in early stage HCC cells promoted metastasis via DUSP10 phosphatase-mediated activation of the ERK pathway. The DUSP10 promoter included putative binding sites for p73 directly implicated in modulation by TP53INP1. Overall, our findings showed how TP53INP1 plays a critical in limiting progression of early stage HCC, with implications for developing new therapeutic strategies to attack metastatic HCC.
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Medicine by Alexandros G. Sfakianakis,Anapafseos 5 Agios Nikolaos 72100 Crete Greece,00302841026182,00306932607174,alsfakia@gmail.com,
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Medicine by Alexandros G. Sfakianakis,Anapafseos 5 Agios Nikolaos 72100 Crete Greece,00302841026182,00306932607174,alsfakia@gmail.com,