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Hofstetter, G., Berger, A., Fiegl, H., Slade, N., Zoric, A., Holzer, B., Schuster, E., Mobus, V.J., Reimer, D., Daxenbichler, G., Marth, C., Zeimet, A.G., Concin, N. and Zeillinger, R. (2010) Alternative Splicing of p53 and p73: The Novel p53 Splice Variant p53δ Is an Independent Prognostic Marker in Ovarian Cancer. Oncogene, 29, 1997-2004. http://dx.doi.org/10.1038/onc.2009.482

has been cited by the following article:

• TITLE: Oncomorphic TP53 Mutations in Gynecologic Cancers Lose the Normal Protein:Protein Interactions with the microRNA Microprocessing Complex

  AUTHORS: Pavla Brachova, Samuel R. Mueting, Eric J. Devor, Kimberly K. Leslie

  KEYWORDS: TP53, p53, miRNA, Drosha, Oncomorphic TP53, Gain of Function

  JOURNAL NAME: Journal of Cancer Therapy, Vol.5 No.6, May 16, 2014

  ABSTRACT: Mutations in the tumor suppressor TP53 occur in almost all advanced ovarian cancers and in many advanced serous endometrial cancers. Mutations in TP53 can alter the function of the p53 protein, and some mutations result in a mutated protein with oncogenic activity. Previously referred to as gain of function (GOF) p53 proteins, we now term these “oncomorphic” mutations to better describe their function as oncogenes. We reviewed the data from The Cancer Genome Atlas (TCGA) and demonstrate that of the patients diagnosed with endometrial cancer that harbor TP53 mutations, approximately 30% of these mutations are oncomorphic. In ovarian cancer, approximately 20% are oncomorphic. The wild type (WT) p53 protein transactivates genes and micro-RNAs (miRNAs) necessary in the response to cellular stress, which turn off growth and induce apoptosis. In addition to direct transcriptional activation, WT p53 also acts through protein:protein interactions with Drosha and the miRNA processing complex to mediate rapid, enhanced processing of a subset of anti-growth miRNAs. We validated the interaction of WT p53 with the Drosha complex in the cell line UCI-107. We observed that miRNAs that inhibit the expression of oncogenes were induced. Specifically, some miRNAs were induced very rapidly over minutes, consistent with enhanced processing, while others required hours, consistent with transcriptional activation. In contrast, the most common oncomorphic TP53 mutations failed to interact with the Drosha complex and lost the ability to rapidly induce the miRNAs which inhibit oncogene expression. These studies highlight one mechanism underlying the oncomorphic properties of specific TP53 mutations: loss of the enhanced processing of anti-proliferative miRNAs.