DNA repair-redox enzyme apurinic endonuclease in cervical cancer: Evaluation of redox control of HIF-1 alpha and prognostic significance

Citation
M. Schindl et al., DNA repair-redox enzyme apurinic endonuclease in cervical cancer: Evaluation of redox control of HIF-1 alpha and prognostic significance, INT J ONCOL, 19(4), 2001, pp. 799-802
Citations number
23
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF ONCOLOGY
ISSN journal
10196439 → ACNP
Volume
19
Issue
4
Year of publication
2001
Pages
799 - 802
Database
ISI
SICI code
1019-6439(200110)19:4<799:DREAEI>2.0.ZU;2-L
Abstract
The multifunctional apurinic/apyrimidinic endonuclease (Ape1/ref-1) plays a key role in the human DNA base excision repair pathway. Ape1/ref-1 has als o been shown to be involved in the redox control of transactivation activit ies of hypoxia-inducible factor (HIF)-1 alpha. The aim of our study was to investigate the expression of these proteins in early stage invasive cervic al cancer. Expression of Ape1/ref-1 and HIF-1 alpha was detected immunohist ochemically in 88 samples of cervical cancer stage pT1b. The levels of the proteins were compared and the prognostic influence of Ape1/ref-1 expressio n was investigated. Strong nuclear expression of Ape1/ref-1 was observed in 9 cases (10.2%), moderate in 22 cases (25%), weak in 17 cases (19.3%), and absent in 40 cases (45.5%). Furthermore, no correlation between Ape1/ref-1 and HIF-1 alpha expression was observed (p=0.864). We also found no relati onship of Ape1/ref-1 expression and survival (p >0.05, log-rank test). From these studies, we have concluded that in cervical cancer there is no corre lation between the upstream redox regulatory protein of HIF-1, i.e., Ape1/r ef-1, and HIF-1 alpha expression. However, these studies do not address any functional relationship between the two proteins.