Expression of genetic markers in lymph node metastases compared with theirprimary tumours in head and neck cancer

Citation
Rp. Takes et al., Expression of genetic markers in lymph node metastases compared with theirprimary tumours in head and neck cancer, J PATHOLOGY, 194(3), 2001, pp. 298-302
Citations number
30
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Journal title
JOURNAL OF PATHOLOGY
ISSN journal
00223417 → ACNP
Volume
194
Issue
3
Year of publication
2001
Pages
298 - 302
Database
ISI
SICI code
0022-3417(200107)194:3<298:EOGMIL>2.0.ZU;2-K
Abstract
Regional metastasis is an important factor in the prognosis and treatment o f head and neck squamous cell carcinoma (HNSCC), The results of earlier stu dies suggested the possibility of predicting nodal metastasis in HNSCC usin g biological markers, To identify which factors may be relevant in the meta static behaviour of these tumours, the expression of several markers involv ed in tumour progression was studied in both nodal metastases and their cor responding primary tumours, Expression of p53, Rb, cyclin D1, myc, bcl-2, E GFR, neu, E-cadherin, epithelial cell adhesion molecule (Ep-CAM), and nm23 was studied in 54 primary tumours and their corresponding metastases in pat ients with HNSCC. The expression of most genes involved in tumourigenesis ( p53, Rb, cyclin D1, myc, bcl-2, EGFR, neu, and E-cadherin) was similar in p rimary tumours and metastases, The expression of nm23 and Ep-CAM was found to be more frequently lower than higher in metastases, compared with their primary tumours, Whereas most genetic alterations of primary tumours remain unchanged in metastases, expression of the cell adhesion molecule Ep-CAM a nd of nm23 is more frequently reduced than increased in metastases, compare d with their primary tumours, suggesting relevance to the process of metast asis, This also implies differences in the regulation of markers involved i n tumourigenesis and the process of metastasis. Copyright (C) 2001 John Wil ey & Sons, Ltd.