THE PATHOMORPHOLOGY OF A HUMAN XENOTRANSPLANTED BASALOID-SQUAMOUS CELL-CARCINOMA

Citation
I. Babo et al., THE PATHOMORPHOLOGY OF A HUMAN XENOTRANSPLANTED BASALOID-SQUAMOUS CELL-CARCINOMA, Neoplasma, 45(4), 1998, pp. 210-215
Citations number
15
Categorie Soggetti
Oncology
Journal title
ISSN journal
00282685
Volume
45
Issue
4
Year of publication
1998
Pages
210 - 215
Database
ISI
SICI code
0028-2685(1998)45:4<210:TPOAHX>2.0.ZU;2-7
Abstract
To elucidate some factors related to the malignant phenotype of an ora l tumor with mixed cell population the question has been raised whethe r the biological behavior of the basaloid or the squamous cells show a ny difference in an immunosuppressed host organism. Basaloid squamous cell carcinoma (BSCC) surgically removed from sublingual location was xenotransplanted either subcutaneously or in the oral submucosa and th e histology, ultrastructures, LDH isoenzyme pattern were investigated. The epithelial origin of the established tumor line (HTB-1) could be recognized according to the characteristic epithelial ultrastructures, while the type of the LDH isoenzymes proved its human origin. The squ amous cell population dominating the parent surgical specimen of BSCC regressed during xenotransplantation in the subcutan location, on the contrary the basaloid cells grew and maintained the tumor. Interesting ly the basaloid cells transplanted from the subcutis to the oral submu cosa generated a squamous cell population with an infiltrative growth pattern. The xenografted BSCC offer a promising model to investigate t he contribution of each cell populations in the malignant phenotype. T he presented data indicate that the basaloid cells are responsible for maintaining the tumor cell population, but certain malignant features (i.e. infiltrative growth) is associated to the squamous cells which are generated from the basaloid cells only under specific circumstance s. Thus this particular model system showed that different malignant f eatures could be associated to the basaloid and to the squamous cell c omponent.