Abstract
While the genetic profiles of hereditary colorectal tumors are being unravelled, the mechanisms implicated in their local progression remain to be deciphered. In this work histological features occurring at the invading tumor front were investigated in ten hereditary non-polyposis colorectal cancers (HNPCC). Of eight moderately-differentiated (i.e. gland-forming) adenocarcinomas, six had dilated glands with a thin layer of tumor cells and all eight had dilated glands in which a group of cells was lacking, i.e. with a glandular pore. It was apparent that the thin glandular epithelium was a stage preceding pore formation. In glands with pores, the contents of the neoplastic glands -rich in proteolytic enzymes- were extruded directly into the extracellular matrix (ECM), leading to the local destruction of the juxtaposed matrix. It was assumed that to restore the continuity of the glands new cancer cells would grow from the tip of the free borders of the pore into the damaged ECM, thus guaranteeing a stepwise, but everlasting, tumor progression in untreated patients.
Footnotes
- Received February 27, 2004.
- Accepted April 15, 2004.
- Copyright© 2004 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved