Back to Search
Start Over
Gene expression analysis of aberrant signaling pathways in meningiomas
- Source :
- Biblos-e Archivo. Repositorio Institucional de la UAM, instname, Oncology Letters
- Publication Year :
- 2013
- Publisher :
- Spandidos Publications, 2013.
-
Abstract
- Examining aberrant pathway alterations is one method for understanding the abnormal signals that are involved in tumorigenesis and tumor progression. In the present study, expression arrays were performed on tumor-related genes in meningiomas. The GE Array Q Series HS-006 was used to determine the expression levels of 96 genes that corresponded to six primary biological regulatory pathways in a series of 42 meningiomas, including 32 grade I, four recurrent grade I and six grade II tumors, in addition to three normal tissue controls. Results showed that 25 genes that were primarily associated with apoptosis and angiogenesis functions were downregulated and 13 genes frequently involving DNA damage repair functions were upregulated. In addition to the inactivation of the neurofibromin gene, NF2, which is considered to be an early step in tumorigenesis, variations of other biological regulatory pathways may play a significant role in the development of meningioma<br />This study was partially supported by Fondo de Investigaciones Sanitarias, Ministerio de Ciencia e Innovación, Spain, Grants PI‑08/1849 and PI‑10/1972; and by grant PI‑10‑045 from the Fundación Sociosanitaria de Castilla‑La Mancha, Spain
- Subjects :
- neurofibromin gene
Cancer Research
Signaling pathways
Schwannoma
Medicina
medicine.disease_cause
Bioinformatics
meningioma
Meningioma
Gene expression
medicine
Gene expression arrays
Gene
schwannoma
biology
Oncogene
business.industry
Articles
Cell cycle
medicine.disease
Neurofibromin 1
signaling pathways
Oncology
gene expression arrays
Tumor progression
biology.protein
Cancer research
Carcinogenesis
business
Neurofibromin gene
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Biblos-e Archivo. Repositorio Institucional de la UAM, instname, Oncology Letters
- Accession number :
- edsair.doi.dedup.....c9d328795ebedcf65b83b0de796106df