Lack of functional retinoblastoma protein mediates increased resistance to antimetabolites in human sarcoma cell lines

Proc Natl Acad Sci U S A. 1995 Oct 24;92(22):10436-40. doi: 10.1073/pnas.92.22.10436.


Growth inhibition assays indicated that the IC50 values for methotrexate (MTX) and 5-fluorodeoxyuridine (FdUrd) in HS-18, a liposarcoma cell line lacking retinoblastoma protein (pRB), and SaOS-2, an osteosarcoma cell line with a truncated and nonfunctional pRB, were 10- to 12-fold and 4- to 11-fold higher, respectively, than for the HT-1080 (fibrosarcoma) cell line, which has wild-type pRB. These Rb-/- cell lines exhibited a 2- to 4-fold increase in both dihydrofolate reductase (DHFR) and thymidylate synthase (TS) enzyme activities as well as a 3- to 4-fold increase in mRNA levels for these enzymes compared to the HT-1080 (Rb+/+) cells. This increase in expression was not due to amplification of the DHFR and TS genes. Growth inhibition by MTX and FdUrd was increased and DHFR and TS activities and expression were correspondingly decreased in Rb transfectants of SaOS-2 cells. In contrast, there was no significant difference in growth inhibition among these cell lines for the nonantimetabolites VP-16, cisplatin, and doxorubicin. A gel mobility-shift assay showed that parental SaOS-2 cells had increased levels of free E2F compared to the Rb-reconstituted SaOS-2 cells. These results indicate that pRB defective cells may have decreased sensitivity to growth inhibition by target enzymes encoded by genes whose transcription is enhanced by E2F proteins and suggest mechanisms of interaction between cytotoxic agents and genes involved in cell cycle progression.

Publication types

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

MeSH terms

  • Antimetabolites, Antineoplastic / toxicity*
  • Antineoplastic Agents / toxicity*
  • Base Sequence
  • Bone Neoplasms
  • Cell Division / drug effects
  • Cell Line
  • Cisplatin / toxicity
  • Doxorubicin / toxicity
  • Drug Resistance, Neoplasm / physiology*
  • Etoposide / toxicity
  • Fibrosarcoma
  • Floxuridine / toxicity*
  • Humans
  • Liposarcoma
  • Methotrexate / toxicity*
  • Molecular Sequence Data
  • Oligonucleotide Probes
  • Osteosarcoma
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / metabolism
  • Retinoblastoma Protein / biosynthesis
  • Retinoblastoma Protein / deficiency*
  • Retinoblastoma Protein / metabolism
  • Tetrahydrofolate Dehydrogenase / metabolism
  • Thymidylate Synthase / metabolism
  • Transfection
  • Tumor Cells, Cultured


  • Antimetabolites, Antineoplastic
  • Antineoplastic Agents
  • Oligonucleotide Probes
  • Recombinant Proteins
  • Retinoblastoma Protein
  • Floxuridine
  • Etoposide
  • Doxorubicin
  • Tetrahydrofolate Dehydrogenase
  • Thymidylate Synthase
  • Cisplatin
  • Methotrexate