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

被引:4
|
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
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