Back to Search Start Over

nm23-H1 protein expression in anal canal carcinoma: does it correlate with prognosis?

Authors :
Indinnimeo M
Cicchini C
Stazi A
Giarnieri E
Limiti MR
Ghini C
Vecchione A
Source :
Journal of surgical oncology [J Surg Oncol] 2000 Jun; Vol. 74 (2), pp. 163-6.
Publication Year :
2000

Abstract

Background and Objectives: Anatomic extent is not the sole axis of classification of tumors and of tumor patients relevant to treatment planning and estimation of prognosis. This results in the need to demonstrate an improvement in prognostic assessment and choice of therapy achieved by consideration of factors other than TNM. nm23 protein does prevent tumor from metastasizing and may also play a role in the control of growth and development. The purpose of this study was to elucidate the clinical significance of nm23 expression in human anal canal carcinoma and to evaluate its influence on the outcome of patients after surgery or radiochemotherapy.<br />Methods: Twenty-two patients affected by anal canal carcinoma were evaluated. Each section was incubated with monoclonal antibody nm23 NDPK-A. Immunostaining was considered positive when at least 10% of the tumor cells were immunostained.<br />Results: nm23 immunoreactivity was detected in 6/22 (27.3%) tumors. No significant association was found between nm23 expression and prognosis.<br />Conclusions: The mechanisms causing enhanced nm23-H1 expression in anal canal carcinoma are unknown. Although the level and expression were not correlated with prognosis, activation of nm23-H1 gene might be a prerequisite for oncogenesis in this type of tumor, while an alternate possibility is the modification of cellular characteristics in relation to proliferation and/or differentiation as a consequence of oncogenesis.

Details

Language :
English
ISSN :
0022-4790
Volume :
74
Issue :
2
Database :
MEDLINE
Journal :
Journal of surgical oncology
Publication Type :
Academic Journal
Accession number :
10914829
Full Text :
https://doi.org/10.1002/1096-9098(200006)74:2<163::AID-JSO16>3.0.CO;2-D