Quantitative evaluation of RASSFIA methylation in the non-lesional, regenerative and neoplastic liver

被引:47
作者
Di Gioia, Sonia
Bianchi, Paolo
Destro, Annarita
Grizzi, Fabio
Malesci, Alberto
Laghi, Luigi
Levrero, Massimo
Morabito, Alberto
Roncalli, Massimo [1 ]
机构
[1] Humanitas Clin Inst Rozzano, Dept Pathol, Milan, Italy
[2] Humanitas Clin Inst Rozzano, Mol Genet Lab, Milan, Italy
[3] Humanitas Clin Inst Rozzano, Sci Direct, Milan, Italy
[4] Humanitas Clin Inst Rozzano, Dept Gastroenterol, Milan, Italy
[5] Humanitas Clin Inst Rozzano, Dept Pathol, Milan, Italy
[6] Univ Roma La Sapienza, Gene Express Lab, Fdn Andrea Cesalpino, Rome, Italy
[7] Univ Milan, Milan, Italy
关键词
D O I
10.1186/1471-2407-6-89
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Epigenetic changes during ageing and their relationship with cancer are under the focus of intense research. RASSF1A and NORE1A are novel genes acting in concert in the proapoptotic pathway of the RAS signalling. While NORE1A has not been previously investigated in the human liver, recent reports have suggested that RASSF1A is frequently epigenetically methylated not only in HCC but also in the cirrhotic liver. Methods: To address whether epigenetic changes take place in connection to age and/or to the underlying disease, we investigated RASSF1A and NORE1A gene promoter methylation by conventional methylation specific PCR and Real-Time MSP in a series of hepatitic and non-hepatitic livers harboring regenerative/hyperplastic (cirrhosis/focal nodular hyperplasia), dysplastic ( large regenerative, low and high grade dysplastic nodules) and neoplastic ( hepatocellular adenoma and carcinoma) growths. Results: In the hepatitic liver ( chronic hepatitic/cirrhosis, hepatocellular nodules and HCC) we found widespread RASSF1A gene promoter methylation with a methylation index that increased from regenerative conditions ( cirrhosis) to hepatocellular nodules ( p < 0.01) to HCC ( p < 0.001). In the non-hepatitic liver a consistent pattern of gene methylation was also found in both lesional ( focal nodular hyperplasia and hepatocellular adenoma) and non-lesional tissue. Specifically, hepatocellular adenomas ( HA) showed a methylation index significantly higher than that detected in focal nodular hyperplasia (FNH) ( p < 0.01) and in non-lesional tissue ( p < 0.001). In non-lesional liver also the methylation index gradually increased by ageing ( p = 0.002), suggesting a progressive spreading of methylated cells over time. As opposed to RASSF1A gene promoter methylation, NORE1A gene was never found epigenetically alterated in both hepatitic and non-hepatitic liver. Conclusion: We have shown that in non-lesional, regenerative and neoplastic liver the RASSF1A gene is increasingly methylated, that this condition takes place as an age-related phenomenon and that the early setting and spreading over time of an epigenetically methylated hepatocyte subpopulation, might be related to liver tumorigenesis.
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页数:12
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