<?xml version="1.0" encoding="UTF-8"?><Articles><Article><id>740</id><JournalTitle>YES-ASSOCIATED PROTEIN (YAP) â€“ A PROMISING THERAPEUTIC  TARGET FOR HEPATOCELLULAR CARCINOMA</JournalTitle><Abstract>Hepatocellular carcinoma (HCC), the third leading cause of cancer mortality, carries a dismal prognosis and represents 
a major health problem. A better understanding of the molecular pathways involved in HCC development may represent an 
important approach for the improvement o f the therapeutic strategies for this cancer. The Hippo signalling pathway, a growth suppressive mechanism that antagonizes the transcriptional co-activator Yes-associated protein (YAP), has been recently found 
altered in human HCC. Moreover, using the Resistant-Hepatocyte (R-H) rat model, recently published data established that the 
Hippo  pathway  deregulation  occurs  already  at  the  early  stages  of  HCC  development,  making  this  pathway  an  important 
therapeutic target. Many strategies have been proposed to mod ulate the activity of the Hippo pathway, and in particular that of 
the final effector YAP, most of which require complex gene manipulations, useful to understand the functions of the pathway 
but difficult to apply on patients. One of the few drugs able to  inhibit in vivo the pro-carcinogenic effect of YAP activation is 
verteporfin,  which  disrupts  the  formation  of  the  complex  between  YAP  and  the  TEAD  transcription  factors,  causing  a 
significant reduction of the number and size of preneoplastic foci induced in rats liver by R-H protocol. In this review, we give 
a  short  summary  of  Hippo  pathway,  providing  the  evidences  of  its  deregulation  in  mouse,  rat  and  human  liver  cancer  and 
discuss the possibility to treat HCC with new drugs targeting the transcriptional co-activator YAP</Abstract><Email>andreaperra@omeca.it</Email><articletype>Research</articletype><volume>7</volume><issue>4</issue><year>2016</year><keyword>Liver,Cancer,YAP,Hippo,Therapy,Verteporfin</keyword><AUTHORS>Andrea Perra,Marta Anna Kowalik</AUTHORS><afflication>Oncology and Molecular Pathology Unit, Department of Biomedical Sciences, University of Cagliari, via Porcell 4, 09124  Cagliari, Italy,Oncology and Molecular Pathology Unit, Department of Biomedical Sciences, University of Cagliari, via Porcell 4, 09124  Cagliari, Italy</afflication></Article></Articles>