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Mutant p53 on the Path to Metastasis.
Tang, Qiaosi; Su, Zhenyi; Gu, Wei; Rustgi, Anil K.
Afiliação
  • Tang Q; Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY 10032, USA.
  • Su Z; Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY 10032, USA.
  • Gu W; Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY 10032, USA.
  • Rustgi AK; Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY 10032, USA. Electronic address: akr2164@cumc.columbia.edu.
Trends Cancer ; 6(1): 62-73, 2020 01.
Article em En | MEDLINE | ID: mdl-31952783
ABSTRACT
Metastasis contributes to the vast majority of cancer-related mortality. Regulatory mechanisms of the multistep invasion-metastasis cascade are being unraveled. TP53 is the most frequently mutated gene across human cancers. Accumulating evidence has shown that mutations of TP53 not only lead to loss of function or dominant negative effects, but also promotes a gain of function. Specifically, gain of function mutant p53 promotes cancer cell motility, invasion, and metastasis. Here, we summarize the mechanisms and functions of mutant p53 that foster metastasis in different types of cancers. We also discuss the prognostic value of mutant p53 and current status of therapeutic strategies targeting mutant p53. Future studies will shed light on discovering novel mechanisms of mutant p53-driven cancer metastasis and developing innovative therapeutics to improve clinical outcomes in patients harboring p53 mutations.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Regulação Neoplásica da Expressão Gênica / Proteína Supressora de Tumor p53 / Metástase Neoplásica / Antineoplásicos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Regulação Neoplásica da Expressão Gênica / Proteína Supressora de Tumor p53 / Metástase Neoplásica / Antineoplásicos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article