| Full text | |
| Author(s): |
Cararo-Lopes, Eduardo
[1, 2, 3]
;
Dias, Matheus H.
[2]
;
da Silva, Marcelo S.
[4, 2]
;
Zeidler, Julianna D.
[2, 5]
;
Vessoni, Alexandre T.
[6]
;
Reis, Marcelo S.
[2]
;
Boccardo, Enrique
[7]
;
Armelin, Hugo A.
[2, 3]
Total Authors: 8
|
| Affiliation: | [1] Inst Butantan, Ctr Toxins Immune Response & Cell Signaling, BR-05503900 Sao Paulo, SP - Brazil
[2] Univ Sao Paulo, Inst Quim, Dept Biochem, BR-05508000 Sao Paulo, SP - Brazil
[3] Univ Estado Sao Paulo, Inst Biociencia, Dept Chem & Biol Sci, BR-18618689 Botucatu, SP - Brazil
[4] Rutgers Canc Inst New Jersey, New Brunswick, NJ 08901 - USA
[5] Washington Univ St Louis, Dept Med, St Louis, MO 63110 - USA
[6] Univ Sao Paulo, Inst Biociencias, Dept Microbiol, BR-05508900 Sao Paulo, SP - Brazil
[7] Mayo Clin, Dept Anesthesiol & Perioperat Med, Kogod Aging Ctr, Coll Med, Rochester, MN 55905 - USA
Total Affiliations: 7
|
| Document type: | Journal article |
| Source: | CELL DEATH & DISEASE; v. 12, n. 2 FEB 18 2021. |
| Web of Science Citations: | 1 |
| Abstract | |
Malignant transformation involves an orchestrated rearrangement of cell cycle regulation mechanisms that must balance autonomic mitogenic impulses and deleterious oncogenic stress. Human papillomavirus (HPV) infection is highly prevalent in populations around the globe, whereas the incidence of cervical cancer is 0.15%. Since HPV infection primes cervical keratinocytes to undergo malignant transformation, we can assume that the balance between transforming mitogenic signals and oncogenic stress is rarely attained. We showed that highly transforming mitogenic signals triggered by HRas(G12V) activity in E6E7-HPV-keratinocytes generate strong replication and oxidative stresses. These stresses are counteracted by autophagy induction that buffers the rapid increase of ROS that is the main cause of genotoxic stress promoted by the oncoprotein. As a result, autophagy creates a narrow window of opportunity for malignant keratinocytes to emerge. This work shows that autophagy is crucial to allow the transition of E6E7 keratinocytes from an immortalized to a malignant state caused by HRas(G12V). (AU) | |
| FAPESP's process: | 13/07467-1 - CeTICS - Center of Toxins, Immune-Response and Cell Signaling |
| Grantee: | Hugo Aguirre Armelin |
| Support Opportunities: | Research Grants - Research, Innovation and Dissemination Centers - RIDC |