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Evolutionary Action Score of TP53 Identifies High-Risk Mutations Associated with Decreased Survival and Increased Distant Metastases in Head and Neck Cancer.
Neskey, David M; Osman, Abdullah A; Ow, Thomas J; Katsonis, Panagiotis; McDonald, Thomas; Hicks, Stephanie C; Hsu, Teng-Kuei; Pickering, Curtis R; Ward, Alexandra; Patel, Ameeta; Yordy, John S; Skinner, Heath D; Giri, Uma; Sano, Daisuke; Story, Michael D; Beadle, Beth M; El-Naggar, Adel K; Kies, Merrill S; William, William N; Caulin, Carlos; Frederick, Mitchell; Kimmel, Marek; Myers, Jeffrey N; Lichtarge, Olivier.
Afiliación
  • Neskey DM; Department of Otolaryngology Head and Neck Surgery, Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.
  • Osman AA; Department of Head and Neck Surgery, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Ow TJ; Department of Otolaryngology Head and Neck Surgery, Albert Einstein School of Medicine, Yeshiva University, New York, New York.
  • Katsonis P; Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, Texas.
  • McDonald T; Department of Statistics, Rice University, Houston, Texas.
  • Hicks SC; Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Hsu TK; Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, Texas.
  • Pickering CR; Department of Head and Neck Surgery, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Ward A; Department of Head and Neck Surgery, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Patel A; Department of Head and Neck Surgery, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Yordy JS; Radiation Oncology, UT Southwestern Medical Center, Dallas, Texas.
  • Skinner HD; Department of Thoracic Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Giri U; Department of Experimental Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Sano D; Department of Otolaryngology-Head and Neck Surgery, Yokahama University, Yokahama, Japan.
  • Story MD; Radiation Oncology, UT Southwestern Medical Center, Dallas, Texas. Department of Radiation Oncology, UT Southwestern Medical Center, Dallas, Texas.
  • Beadle BM; Department of Head and Neck Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • El-Naggar AK; Department of Pathology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Kies MS; Department of Thoracic/Head and Neck Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • William WN; Department of Thoracic/Head and Neck Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Caulin C; Department of Head and Neck Surgery, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Frederick M; Department of Head and Neck Surgery, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.
  • Kimmel M; Department of Statistics, Rice University, Houston, Texas.
  • Myers JN; Department of Head and Neck Surgery, The University of Texas M. D. Anderson Cancer Center, Houston, Texas. jmyers@mdanderson.org.
  • Lichtarge O; Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, Texas.
Cancer Res ; 75(7): 1527-36, 2015 Apr 01.
Article en En | MEDLINE | ID: mdl-25634208
TP53 is the most frequently altered gene in head and neck squamous cell carcinoma, with mutations occurring in over two-thirds of cases, but the prognostic significance of these mutations remains elusive. In the current study, we evaluated a novel computational approach termed evolutionary action (EAp53) to stratify patients with tumors harboring TP53 mutations as high or low risk, and validated this system in both in vivo and in vitro models. Patients with high-risk TP53 mutations had the poorest survival outcomes and the shortest time to the development of distant metastases. Tumor cells expressing high-risk TP53 mutations were more invasive and tumorigenic and they exhibited a higher incidence of lung metastases. We also documented an association between the presence of high-risk mutations and decreased expression of TP53 target genes, highlighting key cellular pathways that are likely to be dysregulated by this subset of p53 mutations that confer particularly aggressive tumor behavior. Overall, our work validated EAp53 as a novel computational tool that may be useful in clinical prognosis of tumors harboring p53 mutations.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma de Células Escamosas / Proteína p53 Supresora de Tumor / Neoplasias de Cabeza y Cuello / Neoplasias Pulmonares Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Cancer Res Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma de Células Escamosas / Proteína p53 Supresora de Tumor / Neoplasias de Cabeza y Cuello / Neoplasias Pulmonares Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Cancer Res Año: 2015 Tipo del documento: Article