期刊
JOURNAL OF THE NATIONAL CANCER INSTITUTE
卷 92, 期 16, 页码 1303-1307出版社
NATL CANCER INSTITUTE
DOI: 10.1093/jnci/92.16.1303
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- NCI NIH HHS [4P50CA7097-0452] Funding Source: Medline
Background: Retinoic acid plays an important role in lung development and differentiation, acting primarily via nuclear receptors encoded by the retinoic acid receptor-beta (RAR beta) gene. Because receptor isoforms RAR beta 2 and RAR beta 4 are repressed in human Lung cancers, we investigated whether methylation of their promoter, P2, might lead to silencing of the RAR beta gene in human lung tumors and cell lines. Methods: Methylation of the P2 promoter from small-cell lung cancer (SCLC) and non-small-cell lung cancer (NSCLC) cell lines and tumor samples was analyzed by the methylation-specific polymerase chain reaction (PCR), Expression of RAR beta 2 and RAR beta 4 was analyzed by reverse transcription-PCR, Loss of heterozygosity (LOH) was analyzed by PCR amplification followed by electrophoretic separation of PCR products. Statistical differences were analyzed by Fisher's exact test with continuity correction. Results: The P2 promoter was methylated in 72% (63 of 87) of SCLC and in 41% (52 of 127) of NSCLC tumors and cell lines, and the difference was statistically significant (two-sided P<.001), By contrast, in 57 of 58 control samples, we observed only the unmethylated form of the gene. Four tumor cell lines with unmethylated promoter regions expressed both RAR beta 2 and RAR beta 4, Four tumor lines with methylated promoter regions lacked expression of these isoforms, but demethylation by exposure to 5-aza-2'-deoxycytidine restored their expression. LOH at chromosome 3p24 was observed in 100% (13 of 13) of SCLC lines and 67% (12 of 18) of NSCLC cell lines, and the difference was statistically significant (two-sided P = .028), Conclusions: Methylation of the RAR beta P2 promoter is one mechanism that silences RAR beta 2 and RAR beta 4 expression in many lung cancers, particularly SCLC, Chemical demethylation is a potential approach to lung cancer therapy.
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