Cyclin-dependent kinase 6 (CDK6) amplification in human gliomas identified using two-dimensional separation of

J F Costello1, C Plass, W Arap

  • 1Ludwig Institute for Cancer Research, University of California-San Diego, La Jolla 92093-0660, USA. jfcostello@ucsd.edu

Cancer Research
|April 1, 1997
PubMed

Insights

Researchers discovered tumor-specific amplification of the cyclin-dependent kinase 6 (CDK6) gene in gliomas using Restriction Landmark Genomic Scanning (RLGS). This finding implicates CDK6 in cancer and highlights RLGS for identifying amplified genes.

Area of Science:

  • Oncology
  • Genetics
  • Molecular Biology

Background:

  • DNA amplification drives tumor progression by overexpressing genes related to drug resistance and proliferation.
  • Restriction Landmark Genomic Scanning (RLGS) is a high-resolution technique for detecting amplified DNA segments.

Purpose of the Study:

  • To investigate tumor-specific DNA amplification in gliomas using RLGS.
  • To identify novel amplified genes in human cancers.

Main Methods:

  • Applied RLGS to matched glioma and normal brain DNA samples.
  • Analyzed amplification of the cyclin-dependent kinase 6 (CDK6) gene.
  • Corroborated findings by assessing CDK6 protein levels.

Main Results:

  • Identified tumor-specific amplification of the CDK6 gene in gliomas.
  • Found CDK6 amplification was not coamplified with MET or EGFR genes, suggesting a novel amplicon.
  • Observed increased CDK6 protein levels in gliomas, both amplification-associated and independent.

Conclusions:

  • The CDK6 gene is implicated in genomic amplification in gliomas.
  • RLGS is a valuable tool for identifying and cloning novel amplified genes in cancer.
  • This study reveals a potential new therapeutic target in gliomas.

Related Concept Videos

Karyotyping01:17

Karyotyping

Describing the number and physical features of chromosomes can reveal abnormalities that underlie genetic diseases. This description is facilitated by special staining techniques that produce a particular banding pattern on each chromosome. State-of-the-art techniques make this approach even more powerful, enabling the detection of individual genes that cause disease.A Simple Chromosome Staining Technique Provides Valuable Scientific InsightSome genetic diseases can be detected by looking at...
Positive Regulator Molecules02:39

Positive Regulator Molecules

Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
M-Cdk Drives Transition Into Mitosis02:15

M-Cdk Drives Transition Into Mitosis

Checkpoints throughout the cell cycle serve as safeguards and gatekeepers, allowing the cell cycle to progress in favorable conditions and slow or halt it in problematic ones. This regulation is known as the cell cycle control system.
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...