Letter to the editor

Dear Editor,

Human papillomavirus (HPV) has been proven to be the main cause of cervical cancer worldwide [1]. Most studies, about HPV tumorgenesis, focus on the role that high risk HPV E6, and E7 proteins play [2]. However high risk HPV E5 protein, one of the virus early phase proteins, is demonstrated to have an important effect on cellular and signaling pathways in human cell lines [3]. Many functions have been described for this viral protein, including, cell transforming activity (Fig. 1), influencing cell cycle and growth factors, induction of apoptosis and endoplasmic reticulum (ER) stress, and immune evasion [3]. HPV E5, as a cell transformer, can interact with the 16 KDal subunit of vacuolar-ATPase (V-ATPase) and disrupt acidification of endosomes [4]. This phenomenon enhances epidermal growth factor (EGF) receptor recycling [4]. Additionally, it has been indicated that the E5 protein increases the expression level of Met, a hepatocyte growth factor (HGF) receptor, promoting transformed cell invasiveness [5]. E5 is also shown to be bonded with an A4 protein, a transmembrane lipoprotein of the endoplasmic reticulum, thus regulating proliferation of infected cells [6]. With all of this considered, it is highly suggested that the HPV E5 protein should be acknowledged as an oncoprotein of HPV. Especially, for the production of DNA-based vaccines this can be of utmost importance. As HPV infections are spread more widely around the world [7], also affecting areas that were thought to be protected by it due to more conservative sexual conduct [8], DNA-based vaccines against HPV should contain not only HPV E6 and E7 coding genes [9], but also E5. Novel vaccines could be used therapeutically as well as in a preventive way. Currently, dispensed vaccines are based on the HPV L1 capsid protein and are able to induce protective immunity (by production of memory cells against L1).

Fig. 1
figure 1

Effect of HPV E5 protein on cellular pathways