pRB2/p130 target genes in non-small lung cancer cells identified by microarray analysis

被引:0
|
作者
Giuseppe Russo
Pier Paolo Claudio
Yan Fu
Peter Stiegler
Zailin Yu
Marcella Macaluso
Antonio Giordano
机构
[1] Sbarro Institute for Cancer Research and Molecular Medicine,Dipartimento di Scienze Odontostomatologiche e Maxillo
[2] College of Science and Technology,Facciali
[3] Temple University,Department of Pathology
[4] Institute of Human Pathology and Oncology,undefined
[5] University of Siena,undefined
[6] Universita' di Napoli ‘Federico II’,undefined
[7] Anatomy and Cell Biology,undefined
[8] Thomas Jefferson University,undefined
[9] Jefferson Medical College,undefined
[10] KCI Room 376,undefined
来源
Oncogene | 2003年 / 22卷
关键词
lung cancer; Rb2/p130; microarray analysis;
D O I
暂无
中图分类号
学科分类号
摘要
The retinoblastoma gene family consisting of RB/p105, p107, and RB2/p130 cooperate to regulate cell-cycle progression through the G1 phase of the cell cycle. Previous data demonstrated an independent role for the reduction or loss of pRb2/p130 expression in the formation and/or progression of lung carcinoma. Rb2/p130 is mutated in a human cell line of lung small cell carcinoma as well as in primary lung tumors. To identify potential pRb2/p130 target genes in an unbiased manner, we have utilized an adenovirus-mediated expression system of pRb2/p130 in a non-small lung cancer cell line to identify specific genes that are regulated by pRb2/p130. Using oligonucleotide arrays, a number of Rb2/p130 downregulated genes were identified and their regulation was confirmed by semiquantitative reverse transcription–polymerase chain reaction (RT–PCR) and Western blot analysis. As a result, 40 genes showed greater than 2.0-fold modification in their expression level after the RB2/p130 viral transduction. In conclusion, coupling adenoviral overexpression with microarray and semiquantitative RT–PCR analyses proved to be a versatile strategy for identifying pRb2/p130 target genes and for better understanding the expression profiles of these genes. Our results may also contribute to identifying novel therapeutic biomarkers in lung carcinoma.
引用
收藏
页码:6959 / 6969
页数:10
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