Methylation Status of Lamin A/C in Gastric Cancer Cell Lines

被引:3
作者
Lee, Won Suk [2 ]
Jung, Jae Joon [2 ]
Jeung, Hei-Cheul
Noh, Se Won
Oh, Bong Kyeong
Kim, Ki Yeol
Kim, Tae Soo [3 ]
Chung, Hyun Cheol [2 ,3 ,4 ]
Roh, Jae Kyung [2 ,3 ,4 ]
Rha, Sun Young [1 ,2 ,3 ,4 ]
机构
[1] Yonsei Univ, Coll Med, Canc Metastasis Res Ctr, Yonsei Canc Ctr, Seoul 120752, South Korea
[2] Yonsei Univ, Brain Korea Project Med Sci 21, Seoul 120752, South Korea
[3] Yonsei Canc Res Inst, Yonsei Canc Ctr, Seoul, South Korea
[4] Yonsei Univ, Coll Med, Dept Internal Med, Seoul 120752, South Korea
基金
新加坡国家研究基金会;
关键词
Lamin A/C; Gastric cancer; Methylation; DNA METHYLATION; A-TYPE; GENE; HYPERMETHYLATION; EXPRESSION; CARCINOMA; PROTEINS;
D O I
10.5754/hge11610
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Epigenetic regulations play a role in the development and progression of cancer. Therefore, discovering novel epigenetically regulated genes could provide useful information in understanding cancer. Lamin A/C is an intermediate filament protein whose expression is reported to be suppressed in tissues of gastro-intestinal malignancies. We examined expression of lamin A/C in gastric and colorectal cancer cell lines and its association with DNA methylation. Methodology: The methylation status of CpG island in 19 gastric, 5 colorectal cancer cells and 1 normal colon cell line were examined with methylation-specific PCR using paired methylated and unmethylated primers. The level of mRNA expression of lamin A/C was detected using RT-PCR. Results: Eighteen gastric cancer cell lines showed 95% unmethylation of lamin A/C and 1 cell line showed partial methylation. In colorectal cancer, only 1 out of 5 cancer cell lines (20%) was partially methylated and the remaining cell lines, including 1 normal colon cell line was unmethylated. With RT-PCR, all cell lines demonstrated mRNA expression of lamin A/C regardless of methylation status. Conclusions: We observed that the expression of lamin A/C was not suppressed in gastrointestinal cancer cell lines different from hematologic malignant cells and it is not regulated through DNA methylation.
引用
收藏
页码:1313 / 1318
页数:6
相关论文
共 36 条
[31]   Polyketal copolymers: A new acid-sensitive delivery vehicle for treating acute inflammatory diseases [J].
Yang, Stephen C. ;
Bhide, Mahesh ;
Crispe, Ian N. ;
Pierce, Robert H. ;
Murthy, Niren .
BIOCONJUGATE CHEMISTRY, 2008, 19 (06) :1164-1169
[32]   Pharmacologic inhibition of epigenetic modi. cations, coupled with gene expression profiling, reveals novel targets of aberrant DNA methylation and histone deacetylation in lung cancer [J].
Zhong, S. ;
Fields, C. R. ;
Su, N. ;
Pan, Y-X ;
Robertson, K. D. .
ONCOGENE, 2007, 26 (18) :2621-2634
[33]  
Zhou Hai-yan, 2006, Zhongguo Yi Liao Qi Xie Za Zhi, V30, P431
[34]  
Zhu JD, 2007, J BIOCHEM MOL BIOL, V40, P135
[35]   Expression of human DNA methyltransferase 1 in colorectal cancer tissues and their corresponding distant normal tissues [J].
Zhu, Yi-Min ;
Huang, Qiong ;
Lin, Jie ;
Hu, Yu ;
Chen, Jian ;
Lai, Mao-De .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2007, 22 (06) :661-666
[36]   Nuclear structure in cancer cells [J].
Zink, D ;
Fischer, AH ;
Nickerson, JA .
NATURE REVIEWS CANCER, 2004, 4 (09) :677-687