Telomerase-Specific Replication-Selective Virotherapy for Human Cancer
Purpose: Replication-selective tumor-specific viruses present a novel approach for treating neoplastic disease. These vectors are designed to induce virus-mediated lysis of tumor cells after selective viral propagation within the tumor. Telomerase activation is considered to be a critical step in ca...
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Published in | Clinical cancer research Vol. 10; no. 1; pp. 285 - 292 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Philadelphia, PA
American Association for Cancer Research
01.01.2004
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Subjects | |
Online Access | Get full text |
ISSN | 1078-0432 1557-3265 |
DOI | 10.1158/1078-0432.CCR-1075-3 |
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Summary: | Purpose: Replication-selective tumor-specific viruses present a novel approach for treating neoplastic disease. These vectors are
designed to induce virus-mediated lysis of tumor cells after selective viral propagation within the tumor. Telomerase activation
is considered to be a critical step in carcinogenesis, and its activity is closely correlated with human telomerase reverse
transcriptase (hTERT) expression. We investigated the antitumor effect of the hTERT-specific replication-competent adenovirus
on human cancer cells.
Experimental Design : We constructed an adenovirus 5 vector [tumor- or telomerase-specific replication-competent adenovirus (TRAD)], in which
the hTERT promoter element drives expression of E1A and E1B genes linked with an internal ribosome entry site, and we examined the selective replication and antitumor effect in human
cancer cells in vitro and in vivo .
Results: TRAD induced selective E1A and E1B expression in human cancer cells, but not in normal cells such as human fibroblasts. TRAD replicated efficiently and induced
marked cell killing in a panel of human cancer cell lines, whereas replication as well as cytotoxicity was highly attenuated
in normal human fibroblasts lacking telomerase activity. In nu/nu mice carrying s.c. human lung tumor xenografts, intratumoral injection of TRAD resulted in a significant inhibition of tumor
growth. No evidence of TRAD was identified in tissues outside of the tumors, despite the presence of TRAD in the circulation.
Moreover, TRAD replication in the distant, noninjected tumors was demonstrated.
Conclusions: Our results suggest that the hTERT promoter confers competence for selective replication of TRAD in human cancer cells, an
outcome that has important implications for the treatment of human cancers. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 1078-0432 1557-3265 |
DOI: | 10.1158/1078-0432.CCR-1075-3 |