Variants from the HCT-8 colon-cancer cell line were implanted s.c. and orth
otopically into nude mice. Well differentiated HCT-8/E11 and HCT-8/E41 cell
s have a functional E-cadherin-catenin complex and are non-invasive into pr
ecultured chick heart fragments in vitro whereas poorly differentiated HCT-
8/E11R1 cells are deficient in alpha -catenin protein and invasive in heart
fragments. We investigated whether these differences were maintained in vi
vo. In contrast with in vitro observations, in vivo the 3 HCT-8 variants be
haved very similarly and ail formed undifferentiated tumors. The in vivo in
vasive behavior of HCT-8 cells was site-dependently modulated: HCT-8 cells
invaded when injected into the cecum but not when injected s.c. Metastases
to the liver or lungs were not observed. The composition and expression of
the E-cadherin-catenin complex in nude mouse HCT-8 tumors was the same as i
n HCT-8 cells in culture on solid substrate. We conclude that the in vivo i
nvasive behavior of HCT-8 cells is not determined by whether alpha -catenin
is expressed or not but by as yet unidentified host factors. (C) 2000 Wile
y-Liss, Inc.