An identical, complex TP53 mutation arising independently in two unrelated families with diverse cancer profiles: the complexity of interpreting cancer risk in carriers-Reference-Cited by-同舟云学术

An identical, complex TP53 mutation arising independently in two unrelated families with diverse cancer profiles: the complexity of interpreting cancer risk in carriers

Published:2012-02 Issue:2 Volume:1 Page:e1-e1
ISSN:2157-9024
Container-title:Oncogenesis
language:en
Short-container-title:Oncogenesis

Author:

Pinto E M,Ribeiro R C,Li J,Taja-Chayeb L,Carrasco L F,de Lourdes Peña-Torres M,Vidal-Millán S,Maldonado-Mtz H,Dueñas-González A,McGregor L,Zambetti G P

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Molecular Biology

Link

http://www.nature.com/articles/oncsis20121.pdf

Reference27 articles.

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2. Ribeiro RC, Sandrini F, Figueiredo B, Zambetti GP, Michalkiewicz E, Lafferty AR et al. An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma. Proc Natl Acad Sci USA 2001; 98: 9330–9335.

3. Varley JM . Germline TP53 mutations and Li-Fraumeni syndrome. Hum Mutat 2003; 21: 313–320.

4. Tabori U, Shlien A, Baskin B, Levitt S, Ray P, Alon N et al. TP53 alterations determine clinical subgroups and survival of patients with choroid plexus tumors. J Clin Oncol 2010; 28: 1995–2001.

5. Seidinger AL, Mastellaro MJ, Fortes FP, Assumpcao JG, Cardinalli IA, Ganazza MA et al. Association of the highly prevalent TP53 R337H mutation with pediatric choroid plexus carcinoma and osteosarcoma in Southeast Brazil. Cancer 2011; 117: 2228–2235.

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