Sg. Ronan et al., MERKEL CELL-CARCINOMA - IN-VITRO AND IN-VIVO CHARACTERISTICS OF A NEWCELL-LINE, Journal of the American Academy of Dermatology, 29(5), 1993, pp. 715-722
Background. Few studies exist that describe Merkel cell carcinoma (MCC
) growth characteristics in vitro, in vivo, or both. Objective: Our pu
rpose was to evaluate the pathologic features of MCC implanted into at
hymic mice and to determine cytogenetic abnormalities in the establish
ed cell line. Methods. Tumor tissues from a patient with MCC were grow
n in culture. Cultured cells were karyotyped and inoculated subcutaneo
usly into athymic mice. Nude mouse tumors were reimplanted into other
athymic mice. Tissues from the primary skin tumor and the nude mouse t
umor were processed for light and electron microscopy and immunocytoch
emistry. Results. The cell line showed a doubling time of 64.8 hours.
Xenografts of 4 x 10(6) cells produced tumors in athymic mice with a d
oubling time of 16.1 days. The nude mouse tumors showed pathologic fea
tures similar to those of the primary skin tumor. Cytogenetic studies
showed a t(1;17) (p36;q21) translocation in 100% of the cells. Conclus
ion: MCC implanted into athymic mice retained the pathologic features
of the primary skin tumor and behaved aggressively. The t(1;17) (p36;q
21) translocation may be a marker of an aggressive phenotype.