Transcriptional regulation of differentiation, selective toxicity and ATGCAAT binding of bisbenzimidazole derivatives in human melanoma cells

Wong, S. S. C., Sturm, R. A., Michel, J., Zhang, X. M., Danoy, P. A. C., Jacobs, J. J., Kaushal, A., Dunn, I. S., Parsons, P. G. and Dong, Y. (1994) Transcriptional regulation of differentiation, selective toxicity and ATGCAAT binding of bisbenzimidazole derivatives in human melanoma cells. Biochemical Pharmacology, 47 5: 827-837. doi:10.1016/0006-2952(94)90483-9


Author Wong, S. S. C.
Sturm, R. A.
Michel, J.
Zhang, X. M.
Danoy, P. A. C.
Jacobs, J. J.
Kaushal, A.
Dunn, I. S.
Parsons, P. G.
Dong, Y.
Title Transcriptional regulation of differentiation, selective toxicity and ATGCAAT binding of bisbenzimidazole derivatives in human melanoma cells
Journal name Biochemical Pharmacology   Check publisher's open access policy
ISSN 0006-2952
1873-2968
Publication date 1994-03-01
Sub-type Article (original research)
DOI 10.1016/0006-2952(94)90483-9
Volume 47
Issue 5
Start page 827
End page 837
Total pages 11
Place of publication Philadelphia, PA, United States
Publisher Elsevier
Language eng
Formatted abstract
To study the relationship between the structure of minor groove ligands and their affinity for specific DNA sequences that regulate gene transcription, three analogues of the A-T-specific DNA minor groove ligands Hoechst 33258 and Hoechst 33342 were synthesized with 5, 8 or 12 carbons in an aliphatic chain attached to the phenolic oxygen of the molecule. There was a striking bimodal relationship between toxicity to HeLa cells and the lipophilicity of the five analogues, toxicity being low for the compounds with a free hydroxyl (Hoechst 33258) or a 12-carbon substituent, yet high for the 5-carbon analogue. Selective killing of human melanoma cells compared with normal fibroblasts was observed for the Hoechst analogue with a 12-carbon chain attached. Hoechst 33258 itself was selectively toxic for the MM96E melanoma cell line compared with other cell lines, induced a highly dendritic morphology, increased tyrosinase activity and tyrosinase mRNA but decreased the level of gp75 (TRP-1) mRNA; message for a third pigment gene, Pmel-17, was unchanged. Tyrosinase activity was decreased in the resistant A2058 melanoma cell line and transcription was affected to a lesser extent than in MM96E. Expression of gp75 protein and two intermediate filament proteins was inhibited by Hoechst 33258 in MM96E cells. There was no major difference in the amount of 125I-Hoechst 33258 taken up by sensitive and resistant cells. of the five derivatives studied, the parent drug Hoechst 33258 and the 2-carbon analogue (Hoechst 33342) were found to have the most inhibitory effect on affinity of octamer binding proteins for the ATGCAAAT consensus sequence found in the promoter region of certain genes associated with proliferation and differentiation. In contrast to Distamycin A (also an A-T-specific minor groove ligand), Hoechst 33258 displaced proteins already bound to the octamer motif. The G-C ligand chromomycin A 3 exhibited a different spectrum of cell toxicity and tyrosinase stimulation compared with Hoechst 33258. Chromomycin A 3 but not Hoechst 33258, strongly inhibited the zinc-dependent transcriptional activity of the sheep metallothionein-Ia promoter in reporter gene assays of transfected cells. Since the six metal-responsive elements of the promoter are GC-rich, this provides independent evidence for the sequence-specificity of transcriptional inactivation by one of these drugs in melanoma cells. Overall, the results suggest that Hoechst 33258 acts by inhibiting the transcription of specific genes, cell lines evidently differing in the accessibility to drugs of certain A-T-rich sequences.
Keyword Hoechst 33258
Chromomycin A3
Octamer-binding proteins
Tyrosinase
Sequence specificity
GP75
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collection: Institute for Molecular Bioscience - Publications
 
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