BioMed Central home | Journals A-Z | Feedback | My details

Open AccessResearch

Implications of tyrosine phosphoproteomics in cervical carcinogenesis

Bernice L Robinson-Bennett1, James DeFord2, Concepcion Diaz-Arrastia1, Lyuba Levine1, Hui-Qui Wang3, Edward V Hannigan1 and John Papaconstantinou2

1Department of Obstetrics and Gynecology, The University of Texas Medical Branch, Galveston, Texas, USA

2Department of Biochemistry and Molecular Biology, The University of Texas and Medical Branch, Galveston, Texas, USA

3Department of Histology, The University of Texas Medical Branch, Galveston, Texas, USA

Journal of Carcinogenesis 2008, 7:2doi:10.1186/1477-3163-7-2

Published: 17 July 2008

Abstract

Background

Worldwide cervical cancer remains a leading cause of mortality from gynecologic malignancies. The link between cervical cancer and persistent infection with HPV has been established. At a molecular level little is known about the transition from the precancerous state to invasive cancer. To elucidate this process, cervical biopsies from human specimens were obtained from precancerous state to stage III disease.

Methods

Cervical biopsies were obtained from patients with a diagnosis of cervical cancer undergoing definitive surgery or staging operation. Biopsies were obtained from patients with precancerous lesions at the time of their excisional procedure. Control samples were obtained from patients undergoing hysterectomy for benign conditions such as fibroids. Samples were subjected to proteomic profiling using two dimensional gel electrophoresis with subsequent trypsin digestion followed by MALDI-TOF protein identification. Candidate proteins were then further studied using western blotting, immunoprecipitation and immunohistochemistry.

Results

Annexin A1 and DNA-PKcs were found to be differentially expressed. Phosphorylated annexin A1 was up regulated in diseased states in comparison to control and its level was strongly detected in the serum of cervical cancer patients compared to controls. DNA-PKcs was noted to be hyperphosphorylated and fragmented in cancer when compared to controls. By immunohistochemistry annexin A1 was noted in the vascular environment in cancer and certain precancerous samples.

Conclusion

This study suggests a probable role for protein tyrosine phosphorylation in cervical carcinogenesis. Annexin A1 and DNA-PK cs may have synergistic effects with HPV infection. Precancerous lesions that may progress to cervical cancer may be differentiated from lesions that will not base on similar immunohistochemical profile to invasive squamous cell carcinoma.


© 1999-2009 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.