Antiproliferative effects of the histone deacetylase inhibitor FR901228 on small-cell lung cancer lines and drug-resistant sublines

Int J Cancer. 2003 Mar 20;104(2):238-42. doi: 10.1002/ijc.10921.


FR901228 is a novel histone deacetylase (HDAC) inhibitor, and its antiproliferative effects on non-small cell lung cancer cells have been shown in vitro. However, there have been no reports concerning the effects on small-cell lung cancer (SCLC). We have recently demonstrated that the HDAC inhibitors trichostatin A and sodium butyrate inhibit expression of the catalytic subunit of telomerase (hTERT) mRNA and telomerase activity in prostate cancer cells. The present study was designed to evaluate the effects of FR901228 on proliferation and telomerase activity in SCLC cells in vitro. FR901228 at 5 to 10 nM increased the fraction of cells in the G(2)/M and sub-G(1) phases of the cell-cycle, and inhibited the growth of H69, H526 and H82 cell lines. The expression of hTERT mRNA was inhibited 6 hr after treatment, prior to obvious inhibition of cell growth or cell-cycle distribution shifts. The inhibition of hTERT mRNA expression and telomerase activity was not a consequence of cell-growth arrest or apoptosis. Cycloheximide blocked the suppression of hTERT mRNA induced by FR901228, and the inhibition of hTERT mRNA by FR901228 required newly synthesized proteins. FR901228 also effectively inhibited growth of etoposide-resistant UMCC-1/VP-16, irinotecan-resistant PC-6/SN2-5H and cisplatin-resistant H526/CDDP cells having decreased expression of hTERT mRNA and telomerase activity, as well as their parental cells. This implies that SCLC resistant to these key drugs are not cross-resistant to FR901228. The present study suggests that FR901228 may be a promising drug for chemotherapy of cancers including SCLC, even for refractory or relapsing tumors after conventional chemotherapy.

MeSH terms

  • Anti-Bacterial Agents / pharmacology*
  • Apoptosis / drug effects
  • Carcinoma, Small Cell / enzymology*
  • Carcinoma, Small Cell / genetics
  • Carcinoma, Small Cell / pathology*
  • Cell Cycle / drug effects
  • Cell Division / drug effects
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins / genetics
  • DNA-Binding Proteins
  • Depsipeptides*
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm*
  • Histone Deacetylase Inhibitors*
  • Humans
  • Lung Neoplasms / enzymology*
  • Lung Neoplasms / genetics
  • Lung Neoplasms / pathology*
  • Peptides, Cyclic*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Retinoblastoma Protein / genetics
  • Telomerase / genetics
  • Telomerase / metabolism
  • Time Factors
  • Tumor Cells, Cultured


  • Anti-Bacterial Agents
  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • DNA-Binding Proteins
  • Depsipeptides
  • Histone Deacetylase Inhibitors
  • Peptides, Cyclic
  • RNA, Messenger
  • Retinoblastoma Protein
  • romidepsin
  • Telomerase