cDNA expression array analysis of DNA repair genes in human glioma cells that lack or express DNA-PK

A M Galloway1, J Allalunis-Turner

  • 1Department of Oncology, Cross Cancer Institute, Edmonton, Alberta, Canada.

Radiation Research
|November 30, 2000
PubMed

Insights

Human cancer cells exhibit altered DNA repair gene expression. M059J cells, deficient in DNA-PKcs (PRKDC), show differential expression of DNA repair genes compared to M059K cells, suggesting fundamental changes in cancer cell repair mechanisms.

Area of Science:

  • Molecular Biology
  • Genetics
  • Cancer Research

Background:

  • M059J cells are the sole human cell line lacking DNA-dependent protein kinase catalytic subunit (DNA-PKcs), now PRKDC.
  • M059K cells, from the same tumor, express PRKDC, offering a model to study DNA-PK's role in DNA damage response.
  • Both cell lines originate from tumors, necessitating investigation into DNA repair gene expression in cancer.

Purpose of the Study:

  • To investigate differential expression of DNA repair genes in M059J and M059K cells.
  • To understand how DNA repair mechanisms may be altered in human cancer cells compared to normal tissues.

Main Methods:

  • Utilized Atlas human cancer cDNA expression arrays to compare gene expression profiles.
  • Confirmed differential gene expression using Northern blotting.

Main Results:

  • Identified differential expression of 14 genes between M059J and M059K cells.
  • Observed greater replication factor C 37-kDa subunit mRNA expression in M059J cells.
  • Found reduced DNA ligase IV expression relative to DNA ligase III in both cell lines, irrespective of irradiation.

Conclusions:

  • DNA repair proteins are altered in these human cancer cell lines.
  • DNA repair mechanisms in cancer cells may fundamentally differ from those in normal tissues.

Related Concept Videos

Nucleotide Excision Repair01:38

Nucleotide Excision Repair

DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
DNA Damage Can Stall the Cell Cycle02:36

DNA Damage Can Stall the Cell Cycle

In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
DNA Damage can Stall the Cell Cycle02:36

DNA Damage can Stall the Cell Cycle

In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...