Literature DB >> 7727726

Antisense therapy of cancer.

R Narayanan1.   

Abstract

Binding sites for the NF-kappa B transcription factor complex, composed of two subunits, p50 (NFKB1) and p65 (rel A), are present in many cell adhesion molecules, cytokines, and growth-factor receptors. Antisense techniques were used to establish the role of NF-kappa B in cell growth. Surprisingly, antisense phosphorothioate oligomers to the rel A subunit of NF-kappa B caused a pronounced block of cellular adhesion. Since adhesion plays an important role in diseases including cancer and inflammation, this chance observation was extended to various in vitro and in vivo models. Our results establish the in vivo efficacy of phosphorothioate oligomers.

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Year:  1994        PMID: 7727726

Source DB:  PubMed          Journal:  In Vivo        ISSN: 0258-851X            Impact factor:   2.155


  3 in total

Review 1.  Strategy for designing specific antisense oligonucleotide sequences.

Authors:  M Mitsuhashi
Journal:  J Gastroenterol       Date:  1997-04       Impact factor: 7.527

2.  Efficacy of p120 antisense-mediated therapy for pancreatic cancer.

Authors:  J W Freeman; W E Strodel; P C McGrath
Journal:  J Gastrointest Surg       Date:  1997 Sep-Oct       Impact factor: 3.452

3.  Sequence context of antisense RelA/NF-kappa B phosphorothioates determines specificity.

Authors:  J Y Maltese; H W Sharma; L Vassilev; R Narayanan
Journal:  Nucleic Acids Res       Date:  1995-04-11       Impact factor: 16.971

  3 in total

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