Growth inhibition of human tumor cell lines by antisense oligonucleotides designed to inhibit p120 expression.

Abstract

The human nucleolar antigen p120 was detected with an anti-p120 monoclonal antibody (MAbp120) in most human malignant tumors (Freeman et al., Cancer Research, 48, 1244-1251, 1988). Stable transfection of the sense p120 cDNA caused malignant transformation of NIH/3T3 cells in vitro, and the antisense p120 constructs markedly delayed the growth of these transformed cells (Perlaky et al., Cancer Research, 52, 428-436, 1992). Several p120 antisense phosphorothioate oligonucleotides designed to hybridize with different regions of the p120 sequence were screened on human tumor cell lines in vitro. Marked growth inhibition of HeLa, LOX and HRCC cell lines was found, particularly with antisense p120 oligonucleotide ISIS 3466 in combination with N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTMA); oligonucleotide ISIS 3466 is complementary to a non-translated region at the 3' end of the molecule. Preliminary in vivo studies on human LOX ascites tumor in nude mice showed marked inhibitory effects on tumor growth by the antisense oligonucleotide ISIS 3466 in the presence of DOTMA when treated on alternate days.

• Authors: L Perlaky, Y Saijo, R K Busch, C F Bennett, C K Mirabelli, S T Crooke, H Busch
• Journal: Anti-cancer drug design (Anticancer Drug Des) Vol. 8 Issue 1 Pg. 3-14 (Feb 1993) ISSN: 0266-9536 [Print] United States
• PMID: 8476501 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Antineoplastic Agents
• Neoplasm Proteins
• Nuclear Proteins
• Oligonucleotides, Antisense
• NOP2 protein, human
• Nop2 protein, mouse
• Protein Methyltransferases
• tRNA Methyltransferases

Topics

• Animals
• Antineoplastic Agents (pharmacology)
• Base Sequence
• Cell Division (drug effects)
• Drug Screening Assays, Antitumor
• Gene Expression (drug effects)
• HeLa Cells
• Humans
• Mice
• Mice, Nude
• Molecular Sequence Data
• Neoplasm Proteins (drug effects, genetics)
• Neoplasm Transplantation
• Nuclear Proteins (drug effects, genetics)
• Oligonucleotides, Antisense (pharmacology)
• Protein Methyltransferases
• Tumor Cells, Cultured (drug effects)
• tRNA Methyltransferases