Methylation Profile Difference in Human High-metastatic Large Cell Lung Cancer Cell Line L9981 and Low-metastatic Large Cell Lung Cancer Line NL9980

• Main Authors: Hui LV, Huiqin YAN, Min WANG, Yongwen LI, Haisu WAN, Hongyu LIU, Heng WU, Qinghua ZHOU
• Format: Article
• Language: zho
• Published: Chinese Anti-Cancer Association; Chinese Antituberculosis Association 2010-08-01
• Series: Chinese Journal of Lung Cancer
• Subjects: MeIP chip; DNA methylation; Metastasis; Lung neoplasms
• Online Access: http://www.lungca.org/index.php?journal=01&page=article&op=viewFile&path[]=10.3779%2Fj.issn.1009-3419.2010.08.02&path[]=1640

Background and objective Invasion and metastasis is one of malignant phenotype of lung cancer and the important cause of the death of lung cancer patients. The aim of this study is to explore the methylation profile difference in different metastatic potential cell lines. Methods To compare the DNA methylation profile of two large cell lung cancer cell lines with different metastatic potential by MeIP chip hybridization, hypermethylated and hypomethylated genes of L9981 cell lines were analyzed online in NIH-DAVID, KEGG and MILANO webside. Results Compared with NL9980 cell line, 735 genes are hypermethylated in L9981, including 656 known genes and 79 unknown genes; 809 gene are hypermethylated in L9981, including 698 known genes and 111 unknown genes; the different genes are involved in cell process, signal transduction, cell communication, cell adhesion, cell motility, and angiogenesis. Conclusion Hypermethylation of suppressor genes and negative regulator of signal transduction and hopomethylation of oncogene and cell adhesion molecules (CAMs) in L9981 may promote metastasis of tumor cells.