Korean J Pathol.  2002 Dec;36(6):394-399.

Alterations of 9p21-22 Region Encoding Genes in Primary Glioblastomas

• Doh HJ
• Suh SI
• Kim DW
• Kim IM
• Yim MB
• Son EI
• Kwon KY
• Lee SS
• Kim SP

Abstract

BACKGROUND: Glioblastomas are one of the most common and aggressive malignant glial tumors occuring in the central nervous system. This study analyzed the status of p15INK4b, p14ARF, p16INK4a, MTAP, IFNA, and IFNB genes in 36 primary glioblastomas to investigate whether the inactivation of these genes participate in primary glioblastoma tumorigenesis.
METHODS
We used polymerase chain reaction, polymerase chain reaction/single strand conformational polymorphism (PCR/SSCP) analysis, and methylation-specific PCR.
RESULTS
Homozygous deletions at the p16INK4a gene were detected in 11 cases (30.5%) of 36 primary glioblastomas, and the promoter hypermethylation was found in 3 cases (8.3%) of 36 primary glioblastomas. In mutational analysis for the p16INK4a gene by PCR/SSCP, there was no abnormal mobility-shifted band in 36 cases of primary glioblastomas. The overall frequency of p16INK4a alterations including homozygous deletion and promoter hypermethylation in 36 primary glioblastomas was 38.8% (14 of 36). Deletions of p15INK4b were noted in 4 cases (11.1%), whereas deletions of the p14ARF and MTAP genes were detected in 1 case of 36 cases of primary glioblastomas. But deletions of the INFA and B genes were not found.
CONCLUSIONS
These results suggest that alterations of the p16INK4a gene can be important mechanisms of the tumorigenesis of primary glioblastomas, and the p16INK4a gene is inactivated by mechanisms including homozygous deletion and promoter hypermethylation.

Keyword

Brain Neoplasms; Glioblastoma; Chromosomes; Human; Pair 9; Genes; p16

MeSH Terms

Brain Neoplasms
Carcinogenesis
Central Nervous System
Genes, p16
Glioblastoma*
Humans
Polymerase Chain Reaction
Tumor Suppressor Protein p14ARF
Tumor Suppressor Protein p14ARF