The anaphase promoting complex: a critical target for viral proteins and anti-cancer drugs

UMMS Affiliation

Program in Gene Function and Expression; Program in Molecular Medicine

Publication Date


Document Type



Antineoplastic Agents; Apoptosis; Capsid Proteins; Cell Cycle; Cell Division; G2 Phase; Gene Products, tax; Gene Products, vpr; Humans; Models, Biological; Retinoblastoma Protein; Tumor Suppressor Protein p53; *Ubiquitin-Protein Ligase Complexes; Viral Proteins


Life Sciences | Medicine and Health Sciences


The study of animal viruses has provided extraordinary insights into cell cycle dynamics and tumor biology. The significance of the p53 and Rb tumor suppressor proteins, for example, was discovered due to their interactions with viral oncogenes. In the past several years, investigations with four viral proteins, human immunodeficiency virus type 1 (HIV-1) vpr, adenovirus E4orf4, chicken anemia virus (CAV) apoptin and human T lymphotropic virus type I (HTLV-I) Tax, have indicated that there are also critical viral targets involved in G2/M control. In particular, recent studies with E4orf4 and apoptin have shown that they induce G2/M arrest by targeting and inhibiting the anaphase-promoting complex/cyclosome (APC/C). Notably, these two viral proteins induce apoptosis selectively in transformed cells in a p53-independent manner; thus pathways affected by these proteins are of significant therapeutic interest. Further investigation of the underlying mechanism of G2/M arrest and subsequent apoptosis induced by viral APC/C inhibitors may shed light on the mechanisms of current cancer therapies and provide the foundation for developing novel therapeutic targets.

DOI of Published Version



Cell Cycle. 2005 Apr;4(4):560-3. Epub 2005 Apr 16.

Journal/Book/Conference Title

Cell cycle (Georgetown, Tex.)

Related Resources

Link to article in PubMed

PubMed ID