Epsteinarr virus and Kaposi’s sarcoma-associated herpesvirus are closely linked to a variety of malignancies including nonkeratinizing nasopharyngeal carcinoma, gastric adenocarcinoma, Burkitt’s lymphoma, Kaposi’s sarcoma, primary effusion lymphoma, multicentric Castleman’s disease, and various forms of lymphoproliferative disorders. Both EBV and KSHV are latent residents in B lymphocytes and show sporadic reactivation in lymphoepithelial tissues such as tonsils. Lytic reactivation of EBV or KSHV in epithelial cells of the nasopharynx is strongly influenced by the state of differentiation. In addition, XBP-1s, a product of the master gene responsible for B cell differentiation, was recently suggested to be one of the physiological stimuli that trigger the lytic switch of EBV and KSHV in latently infected B cells. For a cycling cell, growth arrest in the G1 phase implies one of the following fates to choose: quiescence, apoptosis, differentiation or senescence. Among these four outcomes, differentiation and senescence share two features in common: dramatic chromosome remodeling and lengthy development 15963531 time. Cell senescence is a biochemical process exhibited by metabolically active cells whose cell cycles are frozen beyond the restriction point in G1 phase. First identified in in vitro cultured cells, cellular senescence occurs both in primary and cancer cell lines. In addition, the limit in proliferative capacity triggered by aberrant mitogenic signals of oncogenes, known as oncogene-induced senescence, is an alternative tumor suppressive mechanism that has been recently validated in vivo. Senescence not only occurs in premalignant cells, but also appears in malignant tumors. In the latter case, senescence was usually produced by the removal of an essential oncogenic stimulus or the restoration of a tumor suppressor. For example, ablation of c-Myc in transgenic mouse models induced rapid tumor regression associated with senescence; systemic expression of a dominant-interfering Myc mutant in a preclinical mouse model with Ras-initiated lung adenocarcinoma triggered rapid tumor regression accompanied by senescence. March 2011 | Volume 6 | Issue 3 | e17809 EBV Rta-Mediated EBV and KSHV Reactivation Lytic replication of herpesvirus occurs preferentially in the G1 phase of the cell cycle. Accumulating evidence indicates that a number of viral immediate-early proteins actively exert a growtharrest function by which the virus induces a less competitive environment for resources required for viral DNA replication. In this regard, when EBV undergoes lytic replication, host cells are protected from apoptosis and the DNA-synthetic machinery is blocked, although the activities of certain S-phase regulators increase. In addition, upon viral infection, ICP0 of herpes simplex virus induces cell cycle arrest in G1 by both p53-mediated and p53-independent pathways. Through the up-regulation of cyclins E and D, the IE2 protein of human cytomegalovirus potently arrests U373 cells and simultaneously blocks cellular DNA synthesis. Conceivably, G1 phase is not only a pivotal stage for cell fate determination, but also is critical for virus fate, namely to maintain latency or to initiate a lytic replication episode. Among the identified immediate-early molecules, RTA is positionally and structurally conserved among the genomes of all gamma-herpesviruses. Ectopic expression of the EBV Rta in epithelial or B cells is CX4945 capable of efficiently inducing the lytic cy Epsteinarr virus and Kaposi’s sarcoma-associated herpesvirus are closely linked to a variety of malignancies including nonkeratinizing nasopharyngeal carcinoma, gastric adenocarcinoma, Burkitt’s lymphoma, Kaposi’s sarcoma, primary effusion lymphoma, multicentric Castleman’s disease, and various forms of lymphoproliferative disorders. Both EBV and KSHV are latent residents in B lymphocytes and show sporadic reactivation in lymphoepithelial tissues such as tonsils. Lytic reactivation of EBV or KSHV in epithelial cells of the nasopharynx is strongly influenced by the state of differentiation. In addition, XBP-1s, a product of the master gene responsible for B cell differentiation, was recently suggested to be 17135238 one of the physiological stimuli that trigger the lytic switch of EBV and KSHV in latently infected B cells. For a cycling cell, growth arrest in the G1 phase implies one of the following fates to choose: quiescence, apoptosis, differentiation or senescence. Among these four outcomes, differentiation and senescence share two features in common: dramatic chromosome remodeling and lengthy development time. Cell senescence is a biochemical process exhibited by metabolically active cells whose cell cycles are frozen beyond the restriction point in G1 phase. First identified in in vitro cultured cells, cellular senescence occurs both in primary and cancer cell lines. In addition, the limit in proliferative capacity triggered by aberrant mitogenic signals of oncogenes, known as oncogene-induced senescence, is an alternative tumor suppressive mechanism that has been recently validated in vivo. Senescence not only occurs in premalignant cells, but also appears in malignant tumors. In the latter case, senescence was usually produced by 
the removal of an essential oncogenic stimulus or the restoration of a tumor suppressor. For example, ablation of c-Myc in transgenic mouse models induced rapid tumor regression associated with senescence; systemic expression of a dominant-interfering Myc mutant in a preclinical mouse model with Ras-initiated lung adenocarcinoma triggered rapid tumor regression accompanied by senescence. March 2011 | Volume 6 | Issue 3 | e17809 EBV Rta-Mediated EBV and KSHV Reactivation Lytic replication of herpesvirus occurs preferentially in the G1 phase of the cell cycle. Accumulating evidence indicates that a number of viral immediate-early proteins actively exert a growtharrest function by which the virus induces a less competitive environment for resources required for viral DNA replication. In this regard, when EBV undergoes lytic replication, host cells are protected from apoptosis and the DNA-synthetic machinery is blocked, although the activities of certain S-phase regulators increase. In addition, upon viral infection, ICP0 of herpes simplex virus induces cell cycle arrest in G1 by both p53-mediated and p53-independent pathways. Through the up-regulation of cyclins E and D, the IE2 protein of human cytomegalovirus potently arrests U373 cells and simultaneously blocks cellular DNA synthesis. Conceivably, G1 phase is not only a pivotal stage for cell fate determination, but also is critical for virus fate, namely to maintain latency or to initiate a lytic replication episode. Among the identified immediate-early molecules, RTA is positionally and structurally conserved among the genomes of all gamma-herpesviruses. Ectopic expression of the EBV Rta in epithelial or B cells is capable of efficiently inducing the lytic cy
