We established new cell lines from head and neck cancer patients for s
tudies of adhesion molecules and cellular behavior in nine patients wi
th primary or metastatic cancer treated at the Asan Medical Center. Ex
plant cultures of fresh tumor tissue were used to develop new permanen
t tumor cell lines. Lines were tested for tumor formation and histolog
y in nude mice. Flow cytometry and indirect immunofluorescence were us
ed to assess DNA content and expression of the alpha 6, beta 4, and be
ta 1 integrin subunits and the intercellular adhesion molecule 1 (ICAM
-1). In vitro growth patterns and adhesion to plastic were assessed us
ing phase contrast microscopy. AMC-HN-1 to -8 were derived from patien
ts with squamous cell carcinoma. AMC-HN-9 was from an undifferentiated
carcinoma of the parotid gland. The 8 lines we tested produced nude m
ouse tumors that are identical to the histology of the original tumors
. AMC-HN-1, -2, -5, and -9 have epithelioid or spindle cell morphology
with poor cell-to-cell and cell-to-substrate adhesiveness. AMC-HN-3,
-4, -7, and -8 grow as adherent epithelioid monolayers. AMC-HN-6 exhib
its multilayer stratification. Four lines are near diploid, 4 are hype
rdiploid and 1 is hypodiploid. Only three express ICAM-1. All lines ex
press the alpha 6, beta 4, and beta 1 integrin subunits but to differe
nt extent. Four, AMC-HN-1, -2, -5, and -6, express the beta 4 integrin
at low levels, AMC-HN-3, -4, -7, and -9, have intermediate beta 4 exp
ression, and AMC-HN-8 has extremely high beta 4 expression. The AMC-HN
cell lines are representative in vitro models for the study of head a
nd neck cancer biology. Our preliminary results indicate a close relat
ionship between integrin expression and cell adhesion in vitro.