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Quantitative evaluation of RASSF1A methylation in the non-lesional, regenerative and neoplastic liver

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, recen...

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Autores principales: Di Gioia, Sonia, Bianchi, Paolo, Destro, Annarita, Grizzi, Fabio, Malesci, Alberto, Laghi, Luigi, Levrero, Massimo, Morabito, Alberto, Roncalli, Massimo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1479360/
https://www.ncbi.nlm.nih.gov/pubmed/16606445
http://dx.doi.org/10.1186/1471-2407-6-89
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author Di Gioia, Sonia
Bianchi, Paolo
Destro, Annarita
Grizzi, Fabio
Malesci, Alberto
Laghi, Luigi
Levrero, Massimo
Morabito, Alberto
Roncalli, Massimo
author_facet Di Gioia, Sonia
Bianchi, Paolo
Destro, Annarita
Grizzi, Fabio
Malesci, Alberto
Laghi, Luigi
Levrero, Massimo
Morabito, Alberto
Roncalli, Massimo
author_sort Di Gioia, Sonia
collection PubMed
description 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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spelling pubmed-14793602006-06-20 Quantitative evaluation of RASSF1A methylation in the non-lesional, regenerative and neoplastic liver Di Gioia, Sonia Bianchi, Paolo Destro, Annarita Grizzi, Fabio Malesci, Alberto Laghi, Luigi Levrero, Massimo Morabito, Alberto Roncalli, Massimo BMC Cancer Research Article 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. BioMed Central 2006-04-10 /pmc/articles/PMC1479360/ /pubmed/16606445 http://dx.doi.org/10.1186/1471-2407-6-89 Text en Copyright © 2006 Di Gioia et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Di Gioia, Sonia
Bianchi, Paolo
Destro, Annarita
Grizzi, Fabio
Malesci, Alberto
Laghi, Luigi
Levrero, Massimo
Morabito, Alberto
Roncalli, Massimo
Quantitative evaluation of RASSF1A methylation in the non-lesional, regenerative and neoplastic liver
title Quantitative evaluation of RASSF1A methylation in the non-lesional, regenerative and neoplastic liver
title_full Quantitative evaluation of RASSF1A methylation in the non-lesional, regenerative and neoplastic liver
title_fullStr Quantitative evaluation of RASSF1A methylation in the non-lesional, regenerative and neoplastic liver
title_full_unstemmed Quantitative evaluation of RASSF1A methylation in the non-lesional, regenerative and neoplastic liver
title_short Quantitative evaluation of RASSF1A methylation in the non-lesional, regenerative and neoplastic liver
title_sort quantitative evaluation of rassf1a methylation in the non-lesional, regenerative and neoplastic liver
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1479360/
https://www.ncbi.nlm.nih.gov/pubmed/16606445
http://dx.doi.org/10.1186/1471-2407-6-89
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