Identification and functional characterization of molecular markers involved in head and neck tumorigenesis using methylation pattern data

• Grant number: 03/09497-3
• Support Opportunities: Research Projects - Thematic Grants
• Duration: November 01, 2004 - October 31, 2009
• Field of knowledge: Biological Sciences - Genetics - Human and Medical Genetics
• Principal Investigator: Sandro Roberto Valentini
• Grantee: Sandro Roberto Valentini
• Host Institution: Faculdade de Ciências Farmacêuticas (FCFAR). Universidade Estadual Paulista (UNESP). Campus de Araraquara. Araraquara , SP, Brazil
• Pesquisadores principais: Anamaria Aranha Camargo ; Dirce Maria Carraro ; Paula Rahal

Abstract

Methylation of cytosines in CpG dinucleotides generally leads to the repression of gene expression and is involved in a diversity of normal biological processes such as control of development, protection of the genome against transposable elements, genomic imprinting and X chromosome inactivation. Aberrant DNA methylation is strongly implicated in the development of cancer affecting the expression of more than one hundred of genes for tumor suppression, proliferation and apoptosis regulation, and DNA repair. This fact means that the study of the DNA methylation and chromatin machinery elements related to gene silencing and the careful characterization of DNA methylation pattems in human cancer is essential. The precise quantification of the methylation status or CpG islands therefore mar be a powerful molecular marker for cancer diagnosis and prognosis. The primary aim of the present project is to profile methylation changes of CpG islands in head and neck carcinomas and to identify candidate biomarkers for diagnosis and prognosis of theses tumors. Also, the present study aims to analyze the structural and functional aspects of the isolated biomarkers and the structural aspects of the DNA methylation and histone acetylation machinery elements. (AU)

Scientific publications

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

BRANTIS-DE-CARVALHO, CARLOS EDUARDO; MAARIFI, GHIZLANE; GONCALVES BOLDRIN, PAULO EDUARDO; ZANELLI, CLESLEI FERNANDO; NISOLE, SEBASTIEN; CHELBI-ALIX, MOUNIRA K.; VALENTINI, SANDRO ROBERTO. MxA interacts with and is modified by the SUMOylation machinery. Experimental Cell Research, v. 330, n. 1, p. 151-163, JAN 1 2015. (03/09497-3, 10/50044-6)