Expression and promoter methylation status of HOXA7 gene in pancreatic cancer cell line
10.3760/cma.j.issn.1674-1935.2010.06.017
- VernacularTitle:胰腺癌细胞株HOXA7基因表达及其启动子区甲基化状态
- Author:
Quan PENG
;
Huihua CAI
;
Wentao GAO
;
Zhuyin QIAN
;
Yi MIAO
- Publication Type:Journal Article
- Keywords:
Pancreatic neoplasms;
DNA methylation;
HOXA7 genes;
5-aza-dC
- From:
Chinese Journal of Pancreatology
2010;10(6):430-433
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the expression and methylation status of HOXA7 gene in human pancreatic cancer cell lines, and to explore the relationship between them.Methods HOXA7 mRNA expression of human pancreatic cancer cell lines BxPC3, CFPAC1, PANC1 and SW1990was detected by RT PCR.Bisulfite sequencing PCR (BSP) and combined bisulfite restriction analysis (COBRA) was used to test promoter methylation status.All the cell lines were treated by 5-aza-2-deoxycytidine (5-aza-dC), and HOXA7mRNA expression, methylation status was detected before and after this treatment.Results HOXA7 mRNA was expressed in BxPC3, CFPAC1 and SW1990, while there was no expression of HOXA7 mRNA in PANC1.HOXA7 promoter methylation rates of CFPAC1, BxPC3, PANC1 and SW1990 were 93.16%, 90.65%,90.09% ,52.30%.HOXA7 promoter methylation rate of SW1990 was significantly lower than those in other 3cell lines ( P ＜0.01 ).After 5-aza-dC treatment, HOXA7 mRNA of PANC1 was expressed again, and HOXA7mRNA of BxPC3 was increasingly expressed;while the expression of HOXA7 mRNA in CFPAC1 and SW1990was not significantly changed after 5-aza-dC treatment.Conclusions The expression of HOXA7 mRNA in BxPC3 and PANC1 was closely correlated with promoter hypermethylation, while there was no obvious relation in CFPAC 1 and SW1990.
