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Mapping of homozygous deletions in verified esophageal adenocarcinoma cell lines and xenografts
Author(s) -
Boonstra Jurjen J.,
van Marion Ronald,
Douben Hannie J. C. W.,
Lanchbury Jerry S.,
Timms Kirsten M.,
Abkevich Victor,
Tilanus Hugo W.,
de Klein Annelies,
Dinjens Winand N. M.
Publication year - 2012
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/gcc.20952
Subject(s) - cdkn2a , carcinogenesis , biology , cancer research , gene , cdh1 , cdkn2b , microbiology and biotechnology , genetics , cell , cadherin
Human esophageal adenocarcinoma (EAC) cell lines and xenografts are powerful tools in the search for genetic alterations because these models are composed of pure human cancer cell populations without admixture of normal human cells. In particular detection of homozygous deletions (HDs) is easier using these pure populations of cancer cells. Identification of HDs could potentially lead to the subsequent identification of new tumor suppressor genes (TSGs) involved in esophageal adenocarcinogenesis. Genome wide single nucleotide polymorphism (SNP) arrays were used to identify HDs in 10 verified EAC cell lines and nine EAC xenografts. In total, 61 HDs (range 1–6 per sample) were detected and confirmed by polymerase chain reaction. Besides HDs observed in common fragile genomic regions ( n = 26), and gene deserts ( n = 8), 27 HDs were located in gene‐containing regions. HDs were noted for known TSGs, including CDKN2A , SMAD4 and CDH3 / CDH1 . Twenty‐two new chromosomal regions were detected harboring potentially new TSGs involved in EAC carcinogenesis. Two of these regions of homozygous loss, encompassing the ITGAV and RUNX1 gene, were detected in multiple samples indicating a potential role in the carcinogenesis of EAC. To exclude culturing artifacts, these last two deletions were confirmed by fluorescent in situ hybridization in the primary tumors of which the involved cell lines and xenografts were derived. In summary, in this report we describe the identification of HDs in a series of verified EAC cell lines and xenografts. The deletions documented here are a step forward identifying the key genes involved in EAC development. © 2011 Wiley Periodicals, Inc.