Please use this identifier to cite or link to this item:
Title: Establishment and characterization of a new xenograft-derived human esophageal squamous cell carcinoma cell line SLMT-1 of Chinese origin
Authors: Tang, JCO 
Wan, TSK
Wong, N
Pang, E
Lam, KY
Law, S
Chow, LMC 
Ma, SK
Chan, LC
Wong, J
Srivastava, G
Issue Date: 2001
Publisher: Elsevier
Source: Cancer genetics and cytogenetics, 2001, v. 124, no. 1, p. 36-41 How to cite?
Journal: Cancer genetics and cytogenetics 
Abstract: A new human esophageal cancer cell line, named SLMT-1, was established from a nude-mouse xenograft of a well-differentiated esophageal squamous cell carcinoma (ESCC) of the lower esophagus from a male Hong Kong Chinese patient. SLMT-1, passaged over 34 times and with a doubling time of 31 hours, has the microscopic features of epithelial cells with adherent growth as a monolayer. The general biologic properties of SLMT-1 cells were characterized by (1) a positive test of tumorigenicity obtained by injecting cells subcutaneously into athymic nude mice and observing their development into well-differentiated squamous cell carcinoma; (2) immunohistochemical staining using antibodies (AE1/AE3, CAM5.2 and MAK 6) which show the presence of cytokeratin intermediate filaments; and (3) electron microscopy demonstrating the morphologic features of epithelial cells with the presence of desmosomes. The cytogenetic abnormalities found in both the primary culture and SLMT-1 included der(1;14)(q10;q10), add(1)(p1?), +1, +2, del(3)(q11), +6, +7, i(8)(q10), +8, +10, +11, −13, −15, +16, +17, −18, −19, −Y and marker chromosomes. Additional changes observed in the 34th passage included gains as well as losses of both numerical and structural abnormalities. Comparative genomic hybridization (CGH) indicated copy number gains on chromosomal regions 3q32–qter, 5p, 8p12–p11.2, 11q13–q22 and 13q22–qter, and loss of the Y. The gains of 8p12–p11.2 in SLMT-1 cells are novel to ESCC. Based on its distinct and common characteristics, the SLMT-1 cell line serves as a useful tool for studying the molecular and genetic basis of the pathogenesis of ESCC.
ISSN: 0165-4608
DOI: 10.1016/S0165-4608(00)00317-4
Appears in Collections:Journal/Magazine Article

View full-text via PolyU eLinks SFX Query
Show full item record


Last Week
Last month
Citations as of Feb 15, 2019


Last Week
Last month
Citations as of Feb 11, 2019

Page view(s)

Last Week
Last month
Citations as of Feb 11, 2019

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.