http://www.cnr.it/ontology/cnr/individuo/prodotto/ID4890
Concomitant attivation of Wnt pathway and loss of mismatch repair function in human melanoma (Articolo in rivista)
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- Concomitant attivation of Wnt pathway and loss of mismatch repair function in human melanoma (Articolo in rivista) (literal)
- Anno
- 2008-01-01T00:00:00+01:00 (literal)
- Alternative label
(1) Castiglia D, (1) Bernardini S, (2)r Alvino E, (3) Pagani E, (1) De Luca N, (3) Falcinelli S, (4) Pacchiarotti A, (5) Bonmassar; E,(1) Zambruno G, (3) D'Atri S. (2008)
Concomitant attivation of Wnt pathway and loss of mismatch repair function in human melanoma
in Genes chromosomes & cancer (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- (1) Castiglia D, (1) Bernardini S, (2)r Alvino E, (3) Pagani E, (1) De Luca N, (3) Falcinelli S, (4) Pacchiarotti A, (5) Bonmassar; E,(1) Zambruno G, (3) D'Atri S. (literal)
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- I.F. =3.925
Citations = 5 in Web of knoledge
Citations = 4 in Scopus (literal)
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- 1)LaboratoryofMolecular and Cell Biology,Istituto Dermopatico dell'Immacolata-IRCCS,Rome,Italy
2DepartmentofMedicine,Institute ofNeurobiology and MolecularMedicine,CNR,Rome,Italy
3LaboratoryofMolecular Oncology,Istituto Dermopatico dell'Immacolata-IRCCS,Rome,Italy
4Laboratoryof Histopathology,Istituto Dermopatico dell'Immacolata-IRCCS,Rome,Italy
5DepartmentofNeurosciences,Universityof Rome''TorVergata,''Rome,Italy (literal)
- Titolo
- Concomitant attivation of Wnt pathway and loss of mismatch repair function in human melanoma (literal)
- Abstract
- Constitutive activation of the Wnt pathway plays a key role in the development of colorectal cancer and has also been implicated
in the pathogenesis of other malignancies. Deregulation of Wnt signaling mainly occurs through genetic alterations of
APC, the b-catenin gene (CTNNB1), AXIN1 and AXIN2, leading to stabilization of b-catenin. Physiologically, AXIN2 is transcriptionally
induced on Wnt signaling activation and acts as a negative feedback regulator of the pathway. In colorectal cancer,
mutations in CTNNB1 and AXIN2 occur preferentially in tumors with inactivation of the mismatch repair (MMR) genes MSH2,
MLH1, or PMS2. In this study, the expression of b-catenin and AXIN2, and the mutational status of CTNNB1, APC, and AXIN2
were evaluated in two MMR-deficient (PR-Mel and MR-Mel) and seven MMR-proficient human melanoma cell lines. Only PRMel
and MR-Mel cells showed nuclear accumulation of b-catenin and expression of the AXIN2 gene, and hence, constitutive
activation of Wnt signaling. Mutational analysis identified a somatic heterozygous missense mutation in CTNNB1 exon three
and a germline heterozygous deletion within AXIN2 exon seven in PR-Mel cells, and a somatic biallelic deletion within APC in
MR-Mel cells. Deregulation of Wnt signaling and a defective MMR system were also present in the original tumor of PR and
MR patients. Thus, we describe additional melanomas with mutations in CTNNB1 and APC, identify for the first time a germline
AXIN2 mutation in a melanoma patient and suggest that inactivation of the MMR system and deregulation of the Wnt/b-catenin
signaling pathway cooperate to promote melanoma development and/or progression. (literal)
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