http://www.cnr.it/ontology/cnr/individuo/prodotto/ID223063
Effects of exogenous p53 transduction in thyroid tumor cells with different p53 status. (Articolo in rivista)
- Type
- Label
- Effects of exogenous p53 transduction in thyroid tumor cells with different p53 status. (Articolo in rivista) (literal)
- Anno
- 2000-01-01T00:00:00+01:00 (literal)
- Alternative label
F. MORETTI, S. NANNI, A. FARSETTI, M. NARDUCCI, M. CRESCENZI,
S. GIULIACCI, A. SACCHI, AND A. PONTECORVI (2000)
Effects of exogenous p53 transduction in thyroid tumor cells with different p53 status.
in The Journal of clinical endocrinology and metabolism
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- F. MORETTI, S. NANNI, A. FARSETTI, M. NARDUCCI, M. CRESCENZI,
S. GIULIACCI, A. SACCHI, AND A. PONTECORVI (literal)
- Pagina inizio
- Pagina fine
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- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Molecular Oncogenesis Laboratory, Regina Elena Cancer Institute (F.M., S.N., A.F., M.N., M.C., S.G.,
A.S., A.P.); Institute of Experimental Medicine, Consiglio Nazionale delle Ricerche (F.M., A.F.);
Department of Endocrinology, University La Sapienza (M.N.); Laboratory of Compared Toxicology and
Ecotoxicology, ISS (M.C.); and Institute of Medical Pathology, Catholic University (A.P.), (literal)
- Titolo
- Effects of exogenous p53 transduction in thyroid tumor cells with different p53 status. (literal)
- Abstract
- Recovery of p53 function in undifferentiated thyroid carcinoma
cells carrying an altered p53 gene is able to modify cell tumorigenic
properties. It is not known whether such an effect may also be
achieved in thyroid cancer cells expressing wild-type p53, as in the
majority of differentiated thyroid carcinomas. Effects of p53 transduction
in a thyroid carcinoma cell line (FRO) exhibiting a wild-type
endogenous p53 gene, in comparison to a cell line (WRO) exhibiting
mutant p53, were investigated by using an inducible chimeric construct
containing human p53 complementaryDNAfused to the ligand
binding domain of the estrogen receptor (p53ER). FRO cells were
unaffected by exogenous p53 expression in terms of both proliferation
and viability. On the contrary, p53 reexpression in WRO cells containing
hemizygous mutated p53 allele caused a strong growth inhibition
due to cell accumulation in the G1 phase of the cell cycle. In
addition, exogenous p53 did not influence FRO cell behavior in response
to TSH treatment or modify cell resistance to the chemotherapeutic
agent, doxorubicin. Our results indicate that exogenous expression
of wild-type p53 affects thyroid tumorigenic properties only
in cells carrying an altered p53, whereas it is ineffective in cells
expressing wild-type p53 activity. Therefore, the endogenous p53
status seems to be a major determinant for the effectiveness of a
p53-based gene therapy for thyroid cancer (literal)
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