[Efficacy of hepatic arterial infusion of adriamycin and mitomycin C mixed with degradable starch microspheres for liver metastasis of colorectal cancer--correlation with the mRNA expression of DNA topoisomerase-IIalpha and glutathione-S transferase-pi in primary lesions]

Gan To Kagaku Ryoho. 2004 Oct;31(11):1803-5.
[Article in Japanese]

Abstract

DNA topoisomerase-IIalpha (topo-IIalpha) is a target enzyme of adriamycin (ADM). Glutathione-S-transferase-pi is known to be correlated with the resistance of various anticancer drugs including mitomycin C (MMC) and ADM. Expression levels of topo-IIalpha and GST-pi mRNA of primary colorectal lesions were semi-quantitatively determined by the RT-PCR method in 22 patients with colorectal cancer, who underwent hepatic arterial infusion of ADM and MMC mixed with degradable starch microspheres for synchronous (n=17) or metachronous (n=5) liver metastasis. Expression of topo-IIalpha mRNA/beta-actin mRNA was 0.872+/-0.564 (mean+/-SD) in responders (PR, n=10) and 0.369+/-0.133 in non-responders (SD+PD, n=12) (p=0.047). The relative expression of GST-pi was 0.638+/-0.593 in responders and 1.014+/-0.682 in non-responders (p=0.22). These results suggest that determining the mRNA expression of topo-IIalpha is useful for predicting the efficacy for this regimen, whereas determining the mRNA expression of GST-pi is not.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antigens, Neoplasm
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Biodegradation, Environmental
  • Colorectal Neoplasms / pathology*
  • Combined Modality Therapy
  • DNA Topoisomerases, Type II / analysis*
  • DNA Topoisomerases, Type II / genetics
  • DNA-Binding Proteins
  • Doxorubicin / administration & dosage
  • Embolization, Therapeutic / methods*
  • Female
  • Glutathione S-Transferase pi
  • Glutathione Transferase / analysis*
  • Glutathione Transferase / genetics
  • Hepatic Artery
  • Humans
  • Infusions, Intra-Arterial
  • Isoenzymes / analysis*
  • Isoenzymes / genetics
  • Liver Neoplasms / enzymology
  • Liver Neoplasms / secondary*
  • Liver Neoplasms / therapy*
  • Male
  • Microspheres
  • Middle Aged
  • Mitomycin / administration & dosage
  • RNA, Messenger / analysis
  • Starch / administration & dosage

Substances

  • Antigens, Neoplasm
  • DNA-Binding Proteins
  • Isoenzymes
  • RNA, Messenger
  • Mitomycin
  • Doxorubicin
  • Starch
  • GSTP1 protein, human
  • Glutathione S-Transferase pi
  • Glutathione Transferase
  • DNA Topoisomerases, Type II