학술논문
Genomic and gene expression profiling of minute alterations of chromosome arm 1p in small-cell lung carcinoma cells.
Document Type
Journal Article
Author
Source
Subject
*CANCER
*GENOMICS
*MOLECULAR genetics
*GENE expression
*HUMAN genetics
*SARCOMA
*ANIMAL experimentation
*CELL lines
*CHROMOSOMES
*COMPARATIVE studies
*GENE amplification
*GENE mapping
*IN situ hybridization
*LUNG tumors
*RESEARCH methodology
*MEDICAL cooperation
*POLYMERASE chain reaction
*RESEARCH
*EVALUATION research
*REVERSE transcriptase polymerase chain reaction
*SMALL cell carcinoma
*OLIGONUCLEOTIDE arrays
*GENE expression profiling
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Language
ISSN
0007-0920
Abstract
Genetic alterations occurring on human chromosome arm 1p are common in many types of cancer including lung, breast, neuroblastoma, pheochromocytoma, and colorectal. The identification of tumour suppressors and oncogenes on this arm has been limited by the low resolution of current technologies for fine mapping. In order to identify genetic alterations on 1p in small-cell lung carcinoma, we developed a new resource for fine mapping segmental DNA copy number alterations. We have constructed an array of 642 ordered and fingerprint-verified bacterial artificial chromosome clones spanning the 120 megabase (Mb) 1p arm from 1p11.2 to p36.33. The 1p arm of 15 small-cell lung cancer cell lines was analysed at sub-Mb resolution using this arm-specific array. Among the genetic alterations identified, two regions of recurrent amplification emerged. They were detected in at least 45% of the samples: a 580 kb region at 1p34.2-p34.3 and a 270 kb region at 1p11.2. We further defined the potential importance of these genomic amplifications by analysing the RNA expression of the genes in these regions with Affymetrix oligonucleotide arrays and semiquantitative reverse transcriptase-polymerase chain reaction. Our data revealed overexpression of the genes HEYL, HPCAL4, BMP8, IPT, and RLF, coinciding with genomic amplification. [ABSTRACT FROM AUTHOR]