Data from Akt Activation Synergizes with <i>Trp53</i> Loss in Oral Epithelium to Produce a Novel Mouse Model for Head and Neck Squamous Cell Carcinoma

Abstract

&lt;div&gt;Abstract&lt;p&gt;Head and neck squamous cell carcinoma (HNSCC) is a common human neoplasia with poor prognosis and survival that frequently displays Akt overactivation. Here we show that mice displaying constitutive Akt activity (myrAkt) in combination with &lt;i&gt;Trp53&lt;/i&gt; loss in stratified epithelia develop oral cavity tumors that phenocopy human HNSCC. The myrAkt mice develop oral lesions, making it a possible model of human oral dysplasia. The malignant conversion of these lesions, which is hampered due to the induction of premature senescence, is achieved by the subsequent ablation of &lt;i&gt;Trp53&lt;/i&gt; gene in the same cells &lt;i&gt;in vivo&lt;/i&gt;. Importantly, mouse oral tumors can be followed by &lt;i&gt;in vivo&lt;/i&gt; imaging, show metastatic spreading to regional lymph nodes, and display activation of nuclear factor-κB and signal transducer and activator of transcription-3 pathways and decreased transforming growth factor-β type II receptor expression, thus resembling human counterparts. In addition, malignant conversion is associated with increased number of putative tumor stem cells. These data identify activation of Akt and p53 loss as a major mechanism of oral tumorigenesis &lt;i&gt;in vivo&lt;/i&gt; and suggest that blocking these signaling pathways could have therapeutic implications for the management of HNSCC. [Cancer Res 2009;69(3):1099–108]&lt;/p&gt;&lt;/div&gt;