Decreased levels of topoisomerase II alpha in human renal cell carcinoma lines resistant to etoposide

J Cancer Res Clin Oncol. 1997;123(10):546-54. doi: 10.1007/s004320050103.


Renal cell carcinoma (RCC) displays strong resistance against many chemotherapeutic drugs. Overexpression of P-glycoprotein (Pgp) appears to be part of this resistance. The involvement of another resistance mechanism, involving the decreased activity of DNA topoisomerase II (topoII), remains uncertain. By culturing the human RCC lines RC2 and RC21 in the presence of increasing concentrations of etoposide, we derived the variant sublines RC2E, RC21A and RC21E, that had acquired approximately 30-, 60- and 90-fold resistance to this drug respectively. RC2E, RC21A and RC21E were approximately 50-, 5- and 400-fold cross-resistant to doxorubicin respectively. RC2E and RC21E also showed cross-resistance (approximately 200- and 3500-fold respectively) to vinblastine. Quantitative differences in MDR1 and Pgp expression (elevated in RC2E and RC21E) and topoII alpha (reduced in RC21E and RC21A) were demonstrated using Western blotting and the reverse transcriptase/polymerase chain reaction. Decreased amounts of topoII alpha were reflected in a reduced activity of RC21A and RC21E as measured by unknotting phage P4 DNA. Qualitative changes of the topoII alpha gene, such as point mutations in the motif B/DNBS and DNA-binding regions, or differences in methylation status of the promoter gene of RC21E, were not found. These cell lines represent a model of a solid tumor in which overexpression of Pgp, a combination of increased Pgp and decreased topoII alpha, and a decrease of topoII alpha are represented.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antigens, Neoplasm
  • Antineoplastic Agents / pharmacology
  • Carcinoma, Renal Cell / enzymology*
  • DNA Methylation
  • DNA Topoisomerases, Type II* / metabolism*
  • DNA-Binding Proteins
  • Doxorubicin / pharmacology
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm
  • Etoposide / pharmacology*
  • Gene Expression / drug effects
  • Humans
  • Isoenzymes / metabolism*
  • Kidney Neoplasms / enzymology*
  • Polymorphism, Single-Stranded Conformational
  • RNA, Messenger / genetics
  • RNA, Neoplasm / genetics
  • Tumor Cells, Cultured
  • Vinblastine / pharmacology


  • Antigens, Neoplasm
  • Antineoplastic Agents
  • DNA-Binding Proteins
  • Isoenzymes
  • RNA, Messenger
  • RNA, Neoplasm
  • Vinblastine
  • Etoposide
  • Doxorubicin
  • DNA Topoisomerases, Type II