Abstract | OBJECTIVE: METHODS: Semi-quantitative reverse transcription-PCR (RT-PCR) was used to detect the expression of IGFBP-rP1 in 46 cases of colorectal cancer and their matched normal mucosa. Methylation-specific PCR (MSP) was applied to evaluate the methylation status of 5'CpG island of IGFBP-rP1. Colon cancer cell lines LoVo and SW620 were treated with demethylation agent 5-aza-2'-deoxycytidine (5-aza-dC), followed by RT-PCR and MSP detection. RESULTS: At the mRNA level, the expression of IGFBP-rP1 was higher in colorectal cancer tissue than that in the matched normal mucosa (P < 0.05). IGFBP-rP1 was methylated in 28/46 (60.9%) cases of colorectal cancer and 37/46 (80.4%) matched normal mucosa samples (P < 0.05). A negative correlation was found between IGFBP-rP1 expression and its methylation status. The expression of IGFBP-rP1 was restored in LoVo and SW620 after treatment with 5-aza-dC and MSP confirmation of its demethylation status. No relationships was found between the methylation status and clinicopathologic parameters. CONCLUSIONS:
IGFBP-rP1 expression is negatively correlated with its methylation status in colorectal cancer. DNA methylation is one of the mechanisms regulating the expression of IGFBP-rP1. Hypomethylation of IGFBP-rP1 gene with its overexpression plays an important role in the initiation and development of colorectal cancer.
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Authors | Jie Lin, Yi-Min Zhu, Li-Na Shao, Qiong Huang, Mao-de Lai |
Journal | Zhonghua bing li xue za zhi = Chinese journal of pathology
(Zhonghua Bing Li Xue Za Zhi)
Vol. 37
Issue 8
Pg. 512-6
(Aug 2008)
ISSN: 0529-5807 [Print] China |
PMID | 19094461
(Publication Type: Journal Article)
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Chemical References |
- Insulin-Like Growth Factor Binding Proteins
- RNA, Messenger
- insulin-like growth factor binding protein-related protein 1
- Decitabine
- Azacitidine
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Azacitidine
(analogs & derivatives, pharmacology)
- Cell Line, Tumor
- Colorectal Neoplasms
(genetics)
- CpG Islands
(physiology)
- DNA Methylation
- Decitabine
- Female
- Gene Expression Regulation, Neoplastic
- Humans
- Insulin-Like Growth Factor Binding Proteins
(genetics)
- Male
- Middle Aged
- RNA, Messenger
(metabolism)
- Reverse Transcriptase Polymerase Chain Reaction
(trends)
- Transcription, Genetic
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