Growth and characterization of a cell line from a human primary neuroendocrine carcinoma of the skin (Merkel cell carcinoma) in culture and as xenograft

Citation
K. Krasagakis et al., Growth and characterization of a cell line from a human primary neuroendocrine carcinoma of the skin (Merkel cell carcinoma) in culture and as xenograft, J CELL PHYS, 187(3), 2001, pp. 386-391
Citations number
19
Categorie Soggetti
Cell & Developmental Biology
Journal title
JOURNAL OF CELLULAR PHYSIOLOGY
ISSN journal
00219541 → ACNP
Volume
187
Issue
3
Year of publication
2001
Pages
386 - 391
Database
ISI
SICI code
0021-9541(200106)187:3<386:GACOAC>2.0.ZU;2-V
Abstract
The primary neuroendocrine carcinoma of the skin or Merkel cell carcinoma ( MCC) is a skin tumor with aggressive biological behaviour. Experimental mod els for investigating the biological properties of the tumor are prerequisi te for developing new therapeutic approaches. In this study, we report the establishment and characterisation of a cell line derived from the lymph-no de metastasis of a patient with highly aggressive MCC. Merkel carcinoma cel ls (MCC-1) grew as floating aggregates in suspension cultures for more than two years and over 70 subcultures. The proliferation rate in suspension cu ltures was rather moderate with a population doubling time of 69 h. The imm unocytochemical pattern of the cultured MCC-1 was similar to that of the or iginal tumor with expression of cytokeratin 18, neuron-specific enolase, ne urofilaments, and synaptophysin. In addition, reverse transcriptase polymer ase chain reaction (RT-PCR) revealed presence of chromogranin A mRNA in the MCC-1 cell line. Furthermore, electron microscopy yielded the rare finding of neuroendocrine granules in the cytoplasm of the cultured cells. The cel l line MCC-1 was able to form colonies in soft agar. Nude mice developed so lid tumors with similar histology to the original tumor after subcutaneous and intravenous injections of cultured MCC-1, and malignant ascites was see n after intraperitoneal injection. Also, two MCC-1 sublines were establishe d by reculturing cells from the xenografts grown in vivo and immunocytochem istry confirmed their neuroendocrine origin. The MCC-1 line may thus serve as a model for studying the biology and the metastatic potential of Merkel cell carcinoma. I. Cell. Physiol. 187: 386-391, 2001. (C) 2001 Wiley-Liss, Inc.