Skip to main content
Nucleic Acids Research logoLink to Nucleic Acids Research
. 1996 Feb 15;24(4):737–745. doi: 10.1093/nar/24.4.737

Multiple mechanisms may contribute to the cellular anti-adhesive effects of phosphorothioate oligodeoxynucleotides.

Z Khaled 1, L Benimetskaya 1, R Zeltser 1, T Khan 1, H W Sharma 1, R Narayanan 1, C A Stein 1
PMCID: PMC145673  PMID: 8604318

Abstract

Phosphorothioate oligodeoxynucleotides complementary to the p65 (Rel A) subunit of the NF-kappaB nuclear transcriptional regulatory factor have been suggested to be sequence specific blockers of cellular adhesion. We studied the effects of Rel A antisense, Rel A sense and other phosphorothioate oligodeoxynucleotides on cellular adhesion and found that blockade of adhesion was predominately non-sequence specific. Phosphorothioate oligodeoxynucleotides bind to the extracellular matrix (ECM) of NIH 3T3 cells, and to the ECM elements laminin and fibronectin. By use of a gel mobility shift assay, the association of the A subunit of laminin with a probe 12mer phosphodiester oligodeoxynucleotide could be demonstrated. This interaction was described by a single-site binding equation (K d = 14 microM). Human Rel A antisense and sense oligodeoxynucleotides, and two synthetic persulfated heparin analogs were excellent competitors of the binding of the probe oligodeoxynucleotide to laminin. Taken together, these data indicate that oligodeoxynucleotide binding occurred at or near the heparin-binding site. Competition for 5' 32p- SdT18 (an 18mer phosphorothioate homopolymer of thymidine) binding to fibronectin with the discrete heparin analogs, as well as with SdC28, was also observed. Phosphorothioate oligodeoxynucleotides (Rel A antisense >> Rel A sense) inhibited the binding of laminin to bovine brain sulfatide, but not to its cell surface receptors on MCF-7 cells. By flow cytometric analysis we have also shown, in contrast to what was observed with laminin, that phosphorothioates a non-specifically block the specific binding of fluoresceinated fibronectin to its cell surface receptors on phorbol-12,13-myristate acetate treated Jurkat cells. Blockade of specific binding occurred in the oligodeoxynucleotide treated cells in the presence or absence of oligomer in the media.

Full Text

The Full Text of this article is available as a PDF (164.7 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Cheng Y., Prusoff W. H. Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction. Biochem Pharmacol. 1973 Dec 1;22(23):3099–3108. doi: 10.1016/0006-2952(73)90196-2. [DOI] [PubMed] [Google Scholar]
  2. Ciomei M., Pastori W., Mariani M., Sola F., Grandi M., Mongelli N. New sulfonated distamycin A derivatives with bFGF complexing activity. Biochem Pharmacol. 1994 Jan 20;47(2):295–302. doi: 10.1016/0006-2952(94)90020-5. [DOI] [PubMed] [Google Scholar]
  3. Engel J. Laminins and other strange proteins. Biochemistry. 1992 Nov 10;31(44):10643–10651. doi: 10.1021/bi00159a001. [DOI] [PubMed] [Google Scholar]
  4. Guvakova M. A., Yakubov L. A., Vlodavsky I., Tonkinson J. L., Stein C. A. Phosphorothioate oligodeoxynucleotides bind to basic fibroblast growth factor, inhibit its binding to cell surface receptors, and remove it from low affinity binding sites on extracellular matrix. J Biol Chem. 1995 Feb 10;270(6):2620–2627. doi: 10.1074/jbc.270.6.2620. [DOI] [PubMed] [Google Scholar]
  5. Haimovitz-Friedman A., Balaban N., McLoughlin M., Ehleiter D., Michaeli J., Vlodavsky I., Fuks Z. Protein kinase C mediates basic fibroblast growth factor protection of endothelial cells against radiation-induced apoptosis. Cancer Res. 1994 May 15;54(10):2591–2597. [PubMed] [Google Scholar]
  6. Hardin C. C., Henderson E., Watson T., Prosser J. K. Monovalent cation induced structural transitions in telomeric DNAs: G-DNA folding intermediates. Biochemistry. 1991 May 7;30(18):4460–4472. doi: 10.1021/bi00232a013. [DOI] [PubMed] [Google Scholar]
  7. Hayashi M., Yamada K. M. Divalent cation modulation of fibronectin binding to heparin and to DNA. J Biol Chem. 1982 May 10;257(9):5263–5267. [PubMed] [Google Scholar]
  8. Higgins K. A., Perez J. R., Coleman T. A., Dorshkind K., McComas W. A., Sarmiento U. M., Rosen C. A., Narayanan R. Antisense inhibition of the p65 subunit of NF-kappa B blocks tumorigenicity and causes tumor regression. Proc Natl Acad Sci U S A. 1993 Nov 1;90(21):9901–9905. doi: 10.1073/pnas.90.21.9901. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Khaled Z., Rideout D., O'Driscoll K. R., Petrylak D., Cacace A., Patel R., Chiang L. C., Rotenberg S., Stein C. A. Effects of suramin-related and other clinically therapeutic polyanions on protein kinase C activity. Clin Cancer Res. 1995 Jan;1(1):113–122. [PubMed] [Google Scholar]
  10. Knorre D. G., Vlassov V. V., Zarytova V. F., Karpova G. G. Nucleotide and oligonucleotide derivatives as enzyme and nucleic acid targeted irreversible inhibitors. Chemical aspects. Adv Enzyme Regul. 1985;24:277–299. doi: 10.1016/0065-2571(85)90082-2. [DOI] [PubMed] [Google Scholar]
  11. Lallier T., Bronner-Fraser M. Inhibition of neural crest cell attachment by integrin antisense oligonucleotides. Science. 1993 Jan 29;259(5095):692–695. doi: 10.1126/science.8430321. [DOI] [PubMed] [Google Scholar]
  12. Lux S. E., John K. M., Bennett V. Analysis of cDNA for human erythrocyte ankyrin indicates a repeated structure with homology to tissue-differentiation and cell-cycle control proteins. Nature. 1990 Mar 1;344(6261):36–42. doi: 10.1038/344036a0. [DOI] [PubMed] [Google Scholar]
  13. Maltese J. Y., Sharma H. W., Vassilev L., Narayanan R. Sequence context of antisense RelA/NF-kappa B phosphorothioates determines specificity. Nucleic Acids Res. 1995 Apr 11;23(7):1146–1151. doi: 10.1093/nar/23.7.1146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Narayanan R., Higgins K. A., Perez J. R., Coleman T. A., Rosen C. A. Evidence for differential functions of the p50 and p65 subunits of NF-kappa B with a cell adhesion model. Mol Cell Biol. 1993 Jun;13(6):3802–3810. doi: 10.1128/mcb.13.6.3802. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Neish A. S., Williams A. J., Palmer H. J., Whitley M. Z., Collins T. Functional analysis of the human vascular cell adhesion molecule 1 promoter. J Exp Med. 1992 Dec 1;176(6):1583–1593. doi: 10.1084/jem.176.6.1583. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ojwang J., Elbaggari A., Marshall H. B., Jayaraman K., McGrath M. S., Rando R. F. Inhibition of human immunodeficiency virus type 1 activity in vitro by oligonucleotides composed entirely of guanosine and thymidine. J Acquir Immune Defic Syndr. 1994 Jun;7(6):560–570. [PubMed] [Google Scholar]
  17. Perez J. R., Li Y., Stein C. A., Majumder S., van Oorschot A., Narayanan R. Sequence-independent induction of Sp1 transcription factor activity by phosphorothioate oligodeoxynucleotides. Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):5957–5961. doi: 10.1073/pnas.91.13.5957. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Qwarnström E. E., Ostberg C. O., Turk G. L., Richardson C. A., Bomsztyk K. Fibronectin attachment activates the NF-kappa B p50/p65 heterodimer in fibroblasts and smooth muscle cells. J Biol Chem. 1994 Dec 9;269(49):30765–30768. [PubMed] [Google Scholar]
  19. Rando R. F., Ojwang J., Elbaggari A., Reyes G. R., Tinder R., McGrath M. S., Hogan M. E. Suppression of human immunodeficiency virus type 1 activity in vitro by oligonucleotides which form intramolecular tetrads. J Biol Chem. 1995 Jan 27;270(4):1754–1760. doi: 10.1074/jbc.270.4.1754. [DOI] [PubMed] [Google Scholar]
  20. Steele J. G., Savolainen T. A., Dalton B. A., Smith L., Smith G. J. Adhesion to laminin and expression of laminin in clonally related transformed and control sublines from an alveolar epithelial cell strain. Cancer Res. 1990 Jun 1;50(11):3383–3389. [PubMed] [Google Scholar]
  21. Stein C. A., Cheng Y. C. Antisense oligonucleotides as therapeutic agents--is the bullet really magical? Science. 1993 Aug 20;261(5124):1004–1012. doi: 10.1126/science.8351515. [DOI] [PubMed] [Google Scholar]
  22. Stein C. A., Cleary A. M., Yakubov L., Lederman S. Phosphorothioate oligodeoxynucleotides bind to the third variable loop domain (v3) of human immunodeficiency virus type 1 gp120. Antisense Res Dev. 1993 Spring;3(1):19–31. doi: 10.1089/ard.1993.3.19. [DOI] [PubMed] [Google Scholar]
  23. Stein C. A., Krieg A. M. Problems in interpretation of data derived from in vitro and in vivo use of antisense oligodeoxynucleotides. Antisense Res Dev. 1994 Summer;4(2):67–69. doi: 10.1089/ard.1994.4.67. [DOI] [PubMed] [Google Scholar]
  24. Stein C. A. Suramin: a novel antineoplastic agent with multiple potential mechanisms of action. Cancer Res. 1993 May 15;53(10 Suppl):2239–2248. [PubMed] [Google Scholar]
  25. Stoolman L. M., Wang T. L., Situ R., Varani J. Regulation of fibronectin and laminin binding activity in cultured human lymphoblastic cell lines. J Cell Physiol. 1993 Mar;154(3):593–600. doi: 10.1002/jcp.1041540318. [DOI] [PubMed] [Google Scholar]
  26. Tonkinson J. L., Stein C. A. Patterns of intracellular compartmentalization, trafficking and acidification of 5'-fluorescein labeled phosphodiester and phosphorothioate oligodeoxynucleotides in HL60 cells. Nucleic Acids Res. 1994 Oct 11;22(20):4268–4275. doi: 10.1093/nar/22.20.4268. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Watson P. H., Pon R. T., Shiu R. P. Inhibition of cell adhesion to plastic substratum by phosphorothioate oligonucleotide. Exp Cell Res. 1992 Oct;202(2):391–397. doi: 10.1016/0014-4827(92)90091-l. [DOI] [PubMed] [Google Scholar]
  28. Whelan J., Ghersa P., Hooft van Huijsduijnen R., Gray J., Chandra G., Talabot F., DeLamarter J. F. An NF kappa B-like factor is essential but not sufficient for cytokine induction of endothelial leukocyte adhesion molecule 1 (ELAM-1) gene transcription. Nucleic Acids Res. 1991 May 25;19(10):2645–2653. doi: 10.1093/nar/19.10.2645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Wyatt J. R., Vickers T. A., Roberson J. L., Buckheit R. W., Jr, Klimkait T., DeBaets E., Davis P. W., Rayner B., Imbach J. L., Ecker D. J. Combinatorially selected guanosine-quartet structure is a potent inhibitor of human immunodeficiency virus envelope-mediated cell fusion. Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1356–1360. doi: 10.1073/pnas.91.4.1356. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Yakubov L., Khaled Z., Zhang L. M., Truneh A., Vlassov V., Stein C. A. Oligodeoxynucleotides interact with recombinant CD4 at multiple sites. J Biol Chem. 1993 Sep 5;268(25):18818–18823. [PubMed] [Google Scholar]
  31. Yaswen P., Stampfer M. R., Ghosh K., Cohen J. S. Effects of sequence of thioated oligonucleotides on cultured human mammary epithelial cells. Antisense Res Dev. 1993 Spring;3(1):67–77. doi: 10.1089/ard.1993.3.67. [DOI] [PubMed] [Google Scholar]
  32. Zabrenetzky V. S., Kohn E. C., Roberts D. D. Suramin inhibits laminin- and thrombospondin-mediated melanoma cell adhesion and migration and binding of these adhesive proteins to sulfatide. Cancer Res. 1990 Sep 15;50(18):5937–5942. [PubMed] [Google Scholar]

Articles from Nucleic Acids Research are provided here courtesy of Oxford University Press

RESOURCES