Journal article

Publication year: 2001

Pages: 3563-3567

Journal: Oncogene

Volume number: 20

Issue number: 27

ISSN: 0950-9232

DOI Link: https://doi.org/10.1038/sj.onc.1204469

Publisher: Springer Nature [academic journals on nature.com]

Abstract: 
Loss of heterozygosity at 3p21.3 occurs in more than 90% of small cell lung carcinomas (SCLCs). The Ras association domain family 1 (RASSF1) gene cloned from the lung tumor suppressor locus 3p21.3 consists of two major alternative transcripts, RASSF1A and RASSF1C. Epigenetic inactivation of isoform A (RASSF1A) was observed in 40% of primary non-small cell lung carcinomas and in several tumor cell lines. Transfection of RASSF1A suppressed the growth of lung cancer cells in vitro and in nude mice. Here we have analysed the methylation status of the CPG island promoters of RASSF1A and RASSF1C in primary SCLCs. In 22 of 28 SCLCs (=79%) the promoter of RASSF1A was highly methylated at all CpG sites analysed, None of the SCLCs showed evidence for methylation of the CpG island of RASSF1C. The results suggest that hypermethylation of the CpG island promoter of the RASSF1A gene is associated with SCLC pathogenesis.

Harvard Citation style: Dammann, R., Takahashi, T. and Pfeifer, G. (2001) The CpG island of the novel tumor suppressor gene RASSF1A is intensely methylated in primary small cell lung carcinomas, Oncogene, 20(27), pp. 3563-3567. https://doi.org/10.1038/sj.onc.1204469

APA Citation style: Dammann, R., Takahashi, T., & Pfeifer, G. (2001). The CpG island of the novel tumor suppressor gene RASSF1A is intensely methylated in primary small cell lung carcinomas. Oncogene. 20(27), 3563-3567. https://doi.org/10.1038/sj.onc.1204469