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Cell cycle deregulation in liver lesions of rats with and without genetic predisposition to hepatocarcinogenesis
Author(s) -
Pascale Rosa M.,
Simile Maria M.,
De Miglio Maria R.,
Muroni Maria R.,
Calvisi Diego F.,
Asara Giuseppina,
Casabona Daniela,
Frau Maddalena,
Seddaiu Maria A.,
Feo Francesco
Publication year - 2002
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1053/jhep.2002.33682
Subject(s) - genetic predisposition , deregulation , cell cycle , cancer research , medicine , biology , cancer , economics , disease , macroeconomics
Preneoplastic and neoplastic hepatocytes undergo c‐Myc up‐regulation and overgrowth in rats genetically susceptible to hepatocarcinogenesis, but not in resistant rats. Because c‐Myc regulates the pRb‐E2F pathway, we evaluated cell cycle gene expression in neoplastic nodules and hepatocellular carcinomas (HCCs), induced by initiation/selection (IS) protocols 40 and 70 weeks after diethylnitrosamine treatment, in susceptible Fisher 344 (F344) rats, and resistant Wistar and Brown Norway (BN) rats. No interstrain differences in gene expression occurred in normal liver. Overexpression of c‐ myc, Cyclins D1, E, and A, and E2F1 genes, at messenger RNA (mRNA) and protein levels, rise in Cyclin D1‐CDK4, Cyclin E‐CDK2, and E2F1‐DP1 complexes, and pRb hyperphosphorylation occurred in nodules and HCCs of F344 rats. Expression of Cdk4, Cdk2, p16 INK4A , and p27 KIP1 did not change. In nodules and/or HCCs of Wistar and BN rats, low or no increases in c‐ myc, Cyclins D1, E, and A, and E2F1 expression, and Cyclin‐CDKs complex formation were associated with p16 INK4A overexpression and pRb hypophosphorylation. In conclusion, these results suggest deregulation of G1 and S phases in liver lesions of susceptible rats and block of G1‐S transition in lesions of resistant strains, which explains their low progression capacity.