Mutations in exon 3 of the beta-catenin gene are rare in melanoma cell lines


Autoria(s): Pollock, P. M.; Hayward, N.
Contribuinte(s)

F. J. Lejeune

G. Prota

P. A. Riley

Data(s)

01/01/2002

Resumo

Mutations in exon 3 of the CTNNB1 gene encoding beta-catenin have been reported in colorectal cancer cell lines and tumours. Although one study reported mutations or deletions affecting beta-catenin in 20% of melanoma cell lines, subsequent reports detected a much lower frequency of aberrations in uncultured melanomas. To determine whether this difference in mutation frequency reflected an in vitro culturing artefact, exon 3 of CTNNB1 was screened in a panel of 62 melanoma cell lines. In addition, reverse transcription-polymerase chain reaction (RT-PCR) was performed to detect intragenic deletions affecting exon 3. One out of 62 (1.6%) cell lines was found to carry a mutation, indicating that aberration of the Wnt-l/wingless pathway through activation of beta-catenin is a rare event, even in melanoma cell lines. (C) 2002 Lippincott Williams Wilkins.

Identificador

http://espace.library.uq.edu.au/view/UQ:61510

Idioma(s)

eng

Publicador

Lippincott Williams & Wilkins

Palavras-Chave #Oncology #Dermatology #Medicine, Research & Experimental #Beta-catenjn #Melanoma #Mutation #Hepatocellular Carcinomas #Cancer #Activation #Tcf #Progression #Expression #Frequent #Pathway #Tumors #C1 #321015 Oncology and Carcinogenesis #730108 Cancer and related disorders #1112 Oncology and Carcinogenesis
Tipo

Journal Article