Ak. Virmani et al., Promoter methylation and silencing of the retinoic acid receptor-beta genein lung carcinomas, J NAT CANC, 92(16), 2000, pp. 1303-1307
Background: Retinoic acid plays an important role in lung development and d
ifferentiation, acting primarily via nuclear receptors encoded by the retin
oic acid receptor-beta (RAR beta) gene. Because receptor isoforms RAR beta
2 and RAR beta 4 are repressed in human Lung cancers, we investigated wheth
er methylation of their promoter, P2, might lead to silencing of the RAR be
ta 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-speci
fic polymerase chain reaction (PCR), Expression of RAR beta 2 and RAR beta
4 was analyzed by reverse transcription-PCR, Loss of heterozygosity (LOH) w
as 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, a
nd the difference was statistically significant (two-sided P<.001), By cont
rast, in 57 of 58 control samples, we observed only the unmethylated form o
f the gene. Four tumor cell lines with unmethylated promoter regions expres
sed both RAR beta 2 and RAR beta 4, Four tumor lines with methylated promot
er regions lacked expression of these isoforms, but demethylation by exposu
re to 5-aza-2'-deoxycytidine restored their expression. LOH at chromosome 3
p24 was observed in 100% (13 of 13) of SCLC lines and 67% (12 of 18) of NSC
LC cell lines, and the difference was statistically significant (two-sided
P = .028), Conclusions: Methylation of the RAR beta P2 promoter is one mech
anism that silences RAR beta 2 and RAR beta 4 expression in many lung cance
rs, particularly SCLC, Chemical demethylation is a potential approach to lu
ng cancer therapy.