2002•TumoriRequires access

A preliminary study of loss of heterozygosity on chromosome 3 in glioblastoma

Hu Jie

Open publisher page 0 citations

Abstract

Objective To detect loss of heterozygosity (LOH) in order to locate the deletion areas probably harboring tumor suppressor genes(TSGs) in glioblastoma (GBM). Methods PCR based microsatellite polymorphism analyses were performed to detect LOH on chromosome 3, fluorescence labeled primers and Perkin Elmer 377 DNA Sequencer were applied. Results 50% informative cases of GBM displayed LOH on chromosome 3. 25.6% of informative loci showed LOH in our series, in which the higher frequent LOH were observed in the chromosomal region from loci D3s1614(42.9%) to D3s1565 on 3q24 27 and at loci D3s1569(35.3%) on 3q22 23 and D3s1289 (33.3%) on 3p14.1 14.3. Conclusion Loss of genetic material on chromosome 3 may play an important role on the initiation and progression of GBM. The chromosomal regions from loci D3s1614 to D3s1565 on 3q24 27 and at loci D3s1569 on 3q22 23 and D3s14.3 may harbor novel tumor suppressor genes associated with GBM.

About this research paper

What this paper is about

Objective To detect loss of heterozygosity (LOH) in order to locate the deletion areas probably harboring tumor suppressor genes(TSGs) in glioblastoma (GBM). Methods PCR based microsatellite polymorphism analyses were performed to detect LOH on chromosome 3, fluorescence labeled primers and Perkin Elmer 377 DNA Sequencer were applied. Results 50% informative cases of GBM displayed LOH on chromosome 3. 25.6% of informative loci showed LOH in our series, in which the higher frequent LOH were observed in the chromosomal region from loci D3s1614(42.9%) to D3s1565 on 3q24 27 and at loci D3s1569(35.3%) on 3q22 23 and D3s1289 (33.3%) on 3p14.1 14.3. Conclusion Loss of genetic material on chromosome 3 may play an important role on the initiation and progression of GBM. The chromosomal regions from loci D3s1614 to D3s1565 on 3q24 27 and at loci D3s1569 on 3q22 23 and D3s14.3 may harbor novel tumor suppressor genes associated with GBM.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To detect loss of heterozygosity (LOH) in order to locate the deletion areas probably harboring tumor suppressor genes(TSGs) in glioblastoma (GBM). Methods PCR based microsatellite polymorphism analyses were performed to detect LOH on chromosome 3, fluorescence labeled primers and Perkin Elmer 377 DNA Sequencer were applied. Results 50% informative cases of GBM displayed LOH on chromosome 3. 25.6% of informative loci showed LOH in our series, in which the higher frequent LOH were observed in the chromosomal region from loci D3s1614(42.9%) to D3s1565 on 3q24 27 and at loci D3s1569(35.3%) on 3q22 23 and D3s1289 (33.3%) on 3p14.1 14.3. Conclusion Loss of genetic material on chromosome 3 may play an important role on the initiation and progression of GBM. The chromosomal regions from loci D3s1614 to D3s1565 on 3q24 27 and at loci D3s1569 on 3q22 23 and D3s14.3 may harbor novel tumor suppressor genes associated with GBM.

Key concepts: Loss of heterozygosity, Biology, Genetics, Microsatellite, Chromosome, Glioblastoma, Gene, Molecular biology

Related papers

Back to paper searchBrowse research topicsOriginal source
A preliminary study of loss of heterozygosity on chromosome 3 in glioblastoma — Research Paper | ScholarLens