Frequent homozygous deletion of p16/CDKN2A gene in malignant gliomas of Iranian patients

Zadeh, M.D. and Amini, R. and Firoozray, M. and Derakhshandeh-Peykar, P. (2007) Frequent homozygous deletion of p16/CDKN2A gene in malignant gliomas of Iranian patients. Pakistan Journal of Biological Sciences, 10 (23). pp. 4246-4250.

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Abstract

Homozygous deletion is the main mechanism of CDKN2A gene inactivation in malignant gliomas. However different frequencies were reported for its deletion. In order to find the homozygous deletion frequency among Iranian patients, we have analyzed the status of CDKN2A gene in 40 malignant gliomas and examined their 1α and 2 exons by comparative multiplex Polymerase Chain Reaction (PCR), using D9S171 chromosomal marker as an internal control. We found homozygous deletion in 6 out of 7 cases (85.7) of anaplastic astrocytomas and 20 out of 33 cases (60.6) of glioblastoma multiforme, in total 26 out of 40 cases (65) of malignant gliomas. We also found that CDKN2A deleted patients were younger than CDKN2A non-deleted patients and that exon 2 was deleted more than exon 1α. © 2007 Asian Network for Scientific Information.

Item Type: Article
Additional Information: cited By 7
Subjects: WL Nervous System
QZ Pathology
Divisions: School of Rehabilitation Sciences
Depositing User: parto mrs bakhtminoo
Date Deposited: 26 Jan 2019 11:09
Last Modified: 26 Jan 2019 11:09
URI: http://eprints.iums.ac.ir/id/eprint/9959

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