Abstract | BACKGROUND & AIMS: METHODS: First, we verified in vitro whether ACV-TP-T was a telomerase substrate. Second, we evaluated proliferation and apoptosis in murine (Hepa1-6) and human (Hep3B, HuH7, HepG2) hepatic cancer cells treated with ACV-TP-T. Next, we tested the in vivo treatment efficacy in HBV transgenic mice that spontaneously develop hepatic tumours, and in a syngeneic orthotopic murine model where HCC cells were implanted directly in the liver. RESULTS: In vitro characterization provided direct evidence that the pro-drug was actively metabolized in liver cancer cells by telomerase to release the active form of acyclovir. Alterations in cell cycle and apoptosis were observed following in vitro treatment with ACV-TP-T. In the transgenic and orthotopic mouse models, treatment with ACV-TP-T reduced tumour growth, increased apoptosis, and reduced the proliferation of tumour cells. CONCLUSIONS:
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Authors | Mirko Tarocchi, Simone Polvani, Anna Julie Peired, Giada Marroncini, Massimo Calamante, Elisabetta Ceni, Daniela Rhodes, Tommaso Mello, Giuseppe Pieraccini, Alessandro Quattrone, Claudio Luchinat, Andrea Galli |
Journal | Journal of hepatology
(J Hepatol)
Vol. 61
Issue 5
Pg. 1064-72
(Nov 2014)
ISSN: 1600-0641 [Electronic] Netherlands |
PMID | 24862448
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2014 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved. |
Chemical References |
- Antineoplastic Agents
- Prodrugs
- Thymine Nucleotides
- acycloguanosyl 5'-thymidyltriphosphate
- Guanosine
- Telomerase
- Acyclovir
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Topics |
- Acyclovir
(metabolism, therapeutic use)
- Animals
- Antineoplastic Agents
(metabolism, therapeutic use)
- Apoptosis
(drug effects)
- Carcinoma, Hepatocellular
(drug therapy, metabolism, pathology)
- Cell Line, Tumor
- Guanosine
(analogs & derivatives, metabolism, therapeutic use)
- Hep G2 Cells
- Hepatitis B virus
(genetics, pathogenicity)
- Humans
- Liver Neoplasms
(drug therapy, metabolism, pathology)
- Liver Neoplasms, Experimental
(drug therapy, metabolism, pathology)
- Mice
- Mice, Transgenic
- Prodrugs
(metabolism, therapeutic use)
- Telomerase
(metabolism)
- Thymine Nucleotides
(metabolism, therapeutic use)
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