Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/23560
Title: Establishment and characterization of a new xenograft-derived human esophageal squamous cell carcinoma cell line HKESC-4 of Chinese origin
Authors: Cheung, LCM
Tang, JCO 
Lee, PY
Hu, L
Guan, XY
Tang, WK
Srivastava, G
Wong, J
Luk, JA
Law, S
Issue Date: 2007
Publisher: Elsevier Science Inc
Source: Cancer genetics and cytogenetics, 2007, v. 178, no. 1, p. 17-25 How to cite?
Journal: Cancer Genetics and Cytogenetics 
Abstract: A new human esophageal cancer cell line, HKESC-4, was established from a nude-mouse xenograft of a moderately differentiated esophageal squamous cell carcinoma (ESCC) developed from a 65year-old Hong Kong Chinese man. The cellular characteristics (morphological, electron microscopic, and immunohistochemical studies), tumorigenicity in athymic nude mice, cytogenetic features, and DNA ploidy of the cell line were investigated. The cell line was maintained in vitro for 17 months and passaged 80 times. HKESC-4 grew as a monolayer, with a doubling time of 63 hours. The epithelial nature of HKESC-4 included the presence of cytokeratin intermediate filaments, as shown by antibodies (AE1/AF3, CAM5.2, and MAK 6), and the presence of the tonofilaments, as seen under electron microscopy. HKESC-4 was tumorigenic in nude mice and had DNA aneuploidy. The cytogenetic abnormalities of HKESC-4 included - 1, -2, -3, -4, -5, -6, -7 -8, -9, -10, - 11, - 12, -15, -16, -17, -18, -19, +20, -21, -22, +del(1 1)(p11), +i(11)(q10), and +21 marker chromosomes. Comparative genomic hybridization analysis demonstrated chromosomal gains at 1p36.13, 3q23 similar to q28, 5p15.33 similar to p15.1, 6p25.1 similar to p22.3, 7p21.3p11.2, 7q11.21 similar to q21.13, 8q23.3 similar to q23.3, 11p11.2, 11q12.similar to q13.2, 14q21.3 similar to q32.2, 17p13.3,18p11.32-p11.31, and 20p13 similar to p12.2 and chromosomal losses at 1q12, 2p25.1 similar to p24.3, 13p13-p11.2, 21p, 22p13 similar to p11.2, and Y. The newly established cell line HKESC-4 promises to be a useful tool in future studies of molecular pathogenesis and therapeutics in ESCC.
URI: http://hdl.handle.net/10397/23560
ISSN: 0165-4608
DOI: 10.1016/j.cancergencyto.2007.05.026
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