Mutant TRP53 exerts a target gene-selective dominant-negative effect to drive tumor development

Mutations in , prevalent in human cancer, are reported to drive tumorigenesis through dominant-negative effects (DNEs) over wild-type TRP53 function as well as neomorphic gain-of-function (GOF) activity. We show that five TRP53 mutants do not accelerate lymphomagenesis on a TRP53-deficient backgroun...

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Veröffentlicht in:Genes & development 2018-11, Vol.32 (21-22), p.1420-1429
Hauptverfasser: Aubrey, Brandon J, Janic, Ana, Chen, Yunshun, Chang, Catherine, Lieschke, Elizabeth C, Diepstraten, Sarah T, Kueh, Andrew J, Bernardini, Jonathan P, Dewson, Grant, O'Reilly, Lorraine A, Whitehead, Lachlan, Voss, Anne K, Smyth, Gordon K, Strasser, Andreas, Kelly, Gemma L
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Sprache:eng
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