http://www.cnr.it/ontology/cnr/individuo/prodotto/ID213116
Adenovirus-mediated suppression of HMGI(Y) protein synthesis as potential therapy of human malignant neoplasias (Articolo in rivista)
- Type
- Label
- Adenovirus-mediated suppression of HMGI(Y) protein synthesis as potential therapy of human malignant neoplasias (Articolo in rivista) (literal)
- Anno
- 2000-01-01T00:00:00+01:00 (literal)
- Alternative label
Stefania Scala*, Giuseppe Portella*, Monica Fedele*, Gennaro Chiappetta+, and Alfredo Fusco?§ (2000)
Adenovirus-mediated suppression of HMGI(Y) protein synthesis as potential therapy of human malignant neoplasias
in Proceedings of the National Academy of Sciences of the United States of America
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Stefania Scala*, Giuseppe Portella*, Monica Fedele*, Gennaro Chiappetta+, and Alfredo Fusco?§ (literal)
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- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
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- *Centro di Endocrinologia ed Oncologia Sperimentale del Consiglio Nazionale delle Ricerche cyo Dipartimento di Patologia Cellulare e Molecolare, Facolta`
di Medicina e Chirurgia, Universita` degli Studi di Napoli, 80131 Naples, Italy; +Istituto Nazionale dei Tumori Fondazione Senatore Pascale, via M. Semmola,
80131 Naples, Italy; and ?Dipartimento di Medicina Sperimentale e Clinica, Facolta` di Medicina e Chirurgia di Catanzaro, Universita` degli Studi di
Catanzaro, via Tommaso Campanella 5, 88100 Catanzaro, Italy (literal)
- Titolo
- Adenovirus-mediated suppression of HMGI(Y) protein synthesis as potential therapy of human malignant neoplasias (literal)
- Abstract
- High mobility group I (HMGI) proteins are overexpressed in several
human malignant tumors. We previously demonstrated that inhibition
of HMGI synthesis prevents thyroid cell transformation. Here, we
report that an adenovirus carrying the HMGI(Y) gene in an antisense
orientation (Ad-Yas) induced programmed cell death of two human
thyroid anaplastic carcinoma cell lines (ARO and FB-1), but not normal
thyroid cells. The Ad-Yas virus led to death of lung, colon, and breast
carcinoma cells. A control adenovirus carrying the lacZ gene did not
inhibit the growth of either normal or neoplastic cells. Ad-Yas treatment
of tumors induced in athymic mice by ARO cells caused a drastic
reduction in tumor size. Therefore, suppression of HMGI(Y) protein
synthesis by an HMGI(Y) antisense adenoviral vector may be a useful
treatment strategy in a variety of human malignant neoplasias, in
which HMGI(Y) gene overexpression is a general event. (literal)
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