Ignite Creation Date:
2024-05-05 @ 11:46 AM
Last Modification Date:
2024-10-26 @ 9:13 AM
Study NCT ID:
NCT00125710
Status:
COMPLETED
Last Update Posted:
2016-07-18
First Post:
2005-07-29
Brief Title:
Comparative 2-D Tumor Analysis in Familial Gliomas
Sponsor:
AHS Cancer Control Alberta
Organization:
AHS Cancer Control Alberta
Study Overview
Official Title:
Comparative 2-D Tumor Analysis in Familial Gliomas
Status:
COMPLETED
Status Verified Date:
2014-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The treatment for patients with malignant brain tumors is disappointing The disease is incurable and virtually all patients die from their disease Despite the devastating nature of this illness which affects all age groups its cause remains unexplained Family identification with careful clinical and molecular study have led to the discovery of the genes that cause a number of other devastating diseases like retinoblastoma cystic fibrosis and Huntingtons chorea The investigators propose to study the genetic changes in patients with familial glioma as a first step in identifying the genes that cause these tumors
Detailed Description:
The investigators propose to study the genetic changes in patients with familial glioma as the first step in identifying the genes that cause these tumors With informed consent DNAs from tumor and non-tumor tissue histologic sections pedigrees and detailed clinical information will be acquired for patients with familial gliomas A genomic screening methodology named 2D genomic scanning will be used Differences detected between the tumor and normal tissues blood fibroblasts will identify events occurring in the tumoral process A comparison of the events in familial and sporadic gliomas will outline some of the pathways suspected to be involved both in tumor initiation and progression Briefly DNA fragments are amplified with the polymerase-chain-reaction PCR from tumor and normal tissue using primers designed to identify 100 to 1000 random sites within the genome The PCR primers will hybridize throughout the genome and generate a manageable number of short PCR products that are detected by gel electrophoresis and autoradiography The PCR for both tumor and constitutional tissues are amplified through 20 to 25 cycles to ensure adequate signal but to avoid entering a non-exponential phase of the PCR amplification The products are radiolabelled and then run on a standard sequencing gel The single lane containing labelled PCR products is cut out and then overlaid onto a denaturing grading gel with a 10 to 75 grading of denaturant The labelled DNA is then separated in the second dimension and the DNA is detected by Southern Transfer to nylon membrane or by gel-drying and direct exposure film A direct comparison of PCR signals from the tumor and constitutional tissue identifies the loss or gain of signal which reflects the same phenomena within the genome The isolation and characterization of fragment consistently altered in gliomas will provide the first step in the search for genes responsible in the initiation and progression of gliomas Because of the collaboration among investigators of different centres in Canada the current investigators have a unique opportunity to perform the study on the largest collection of familial gliomas in the world They expect several genomic abnormalities in each tumor Some of these may be seen in several patients Data will be analyzed primarily using descriptive statistics with frequency of genetic abnormalities at different chromosomal locations described
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None