| Full text | |
| Author(s): |
Total Authors: 3
|
| Affiliation: | [1] Universidade de Sao Paulo. Instituto de Ciencias Biomedicas. Departamento de Microbiologia - Brasil
[2] Universidade de Sao Paulo. Instituto de Ciencias Biomedicas. Departamento de Microbiologia - Brasil
[3] Universidade de Sao Paulo. Instituto de Ciencias Biomedicas. Departamento de Microbiologia - Brasil
Total Affiliations: 3
|
| Document type: | Journal article |
| Source: | Clinics; v. 73, 2018-09-06. |
| Abstract | |
Infection with high oncogenic risk human papillomavirus types is the etiological factor of cervical cancer and a major cause of other epithelial malignancies, including vulvar, vaginal, anal, penile and head and neck carcinomas. These agents affect epithelial homeostasis through the expression of specific proteins that deregulate important cellular signaling pathways to achieve efficient viral replication. Among the major targets of viral proteins are components of the DNA damage detection and repair machinery. The activation of many of these cellular factors is critical to process viral genome replication intermediates and, consequently, to sustain faithful viral progeny production. In addition to the important role of cellular DNA repair machinery in the infective human papillomavirus cycle, alterations in the expression and activity of many of its components are observed in human papillomavirus-related tumors. Several studies from different laboratories have reported the impact of the expression of human papillomavirus oncogenes, mainly E6 and E7, on proteins in almost all the main cellular DNA repair mechanisms. This has direct consequences on cellular transformation since it causes the accumulation of point mutations, insertions and deletions of short nucleotide stretches, as well as numerical and structural chromosomal alterations characteristic of tumor cells. On the other hand, it is clear that human papillomavirus-transformed cells depend on the preservation of a basal cellular DNA repair activity level to maintain tumor cell viability. In this review, we summarize the data concerning the effect of human papillomavirus infection on DNA repair mechanisms. In addition, we discuss the potential of exploiting human papillomavirus-transformed cell dependency on DNA repair pathways as effective antitumoral therapies. (AU) | |
| FAPESP's process: | 10/20002-0 - Study of Synthetic Lethality in cells infected with Human Papillomaviruses (HPV) |
| Grantee: | Enrique Mario Boccardo Pierulivo |
| Support Opportunities: | Research Grants - Young Investigators Grants |