Hypersensitivity in DNA mismatch repair-deficient colon carcinoma cells to DNA polymerase reaction inhibitors

Cancer Lett. 2005 Mar 18;220(1):85-93. doi: 10.1016/j.canlet.2004.07.044.

Abstract

We studied the cytotoxic effects of various DNA replication inhibitors on MMR-deficient and -proficient colon carcinoma cell lines. DNA polymerase (pol) inhibitors including aphidicolin and gemcitabine, and hydroxyurea were more toxic (1.7 to 2.8-fold) to hMLH1-deficient HCT116 than to hMLH1-proficient HCT116+ch3. Similarly, pol inhibitors were more toxic to hMSH2-deficient LoVo than to hMSH2-proficient LoVo+ch2. In contrast, DNA topoisomerase I inhibitors, such as CPT-11, SN-38, and topotecan, were more toxic to MMR-proficient cells. Our results suggest that MMR-deficient colon carcinoma cells are hypersensitive to inhibitors of the pol reaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Antineoplastic Agents / pharmacology
  • Aphidicolin / pharmacology
  • Base Pair Mismatch*
  • Carrier Proteins
  • Colonic Neoplasms / genetics*
  • DNA Repair*
  • HCT116 Cells
  • Humans
  • MutL Protein Homolog 1
  • Neoplasm Proteins / metabolism*
  • Nuclear Proteins
  • Nucleic Acid Synthesis Inhibitors*
  • Tumor Cells, Cultured

Substances

  • Adaptor Proteins, Signal Transducing
  • Antineoplastic Agents
  • Carrier Proteins
  • MLH1 protein, human
  • Neoplasm Proteins
  • Nuclear Proteins
  • Nucleic Acid Synthesis Inhibitors
  • Aphidicolin
  • MutL Protein Homolog 1