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  4. Inhibition of α-fetoprotein production in a hepatoma cell line by antisense oligonucleotide analogues
 
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Inhibition of α-fetoprotein production in a hepatoma cell line by antisense oligonucleotide analogues

Journal
Journal of Biochemistry
Journal Volume
117
Journal Issue
5
Pages
1100-1104
Date Issued
1995
Author(s)
Lin S.-B.
Huang S.-S.
Choo K.-B.
PEI-JER CHEN  
Au L.-C.
DOI
10.1093/oxfordjournals.jbchem.a124813
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029013336&doi=10.1093%2foxfordjournals.jbchem.a124813&partnerID=40&md5=6eb9353d59119e3ab69446bcf044675c
https://scholars.lib.ntu.edu.tw/handle/123456789/568881
Abstract
α-Fetoprotein (AFP) is a fetal protein which is absent in adult serum. However, the AFP gene is expressed in some neoplastic cells. According to the literature, AFP may play a role in accelerating the growth of cancer cells. In this report, 15meric antisense oligonucleotide analogues (phosphorothioates and methylphosphonates) and their chimeric forms, which were complementary to different regions of AFP mRNA, were synthesized, and their physical characteristics such as stability, melting temperature, and toxicity were compared. They were examined as to their inhibitory effects on the translation of AFP mRNA in a AFP-producing hepatoma cell line, HuH-7. We found that chimeric oligomers with methylphosphonate or phosphorothioate linkages at both the 5' and 3' ends were more effective than prototypic oligomers. Inhibition of 72% was achieved with a chimeric oligomer against the translational initiation region, at a concentration of 25 μM. No suppressive effect of the oligomers was observed on cell viability or albumin production, indicating the specificity of the inhibition. ? 1995 Oxford University Press.
Subjects
Antisense oligonucleotide; Chimeric; Hepatoma cell line; Inhibition of translation; α-fetoprotein
SDGs

[SDGs]SDG3

Other Subjects
albumin; alpha fetoprotein; antisense oligonucleotide; fetoprotein; messenger rna; methylphosphonic acid; oligodeoxyribonucleotide; article; cancer cell culture; cell viability; culture medium; gene; hepatoma cell; human; human cell; protein synthesis inhibition; translation initiation; alpha-Fetoproteins; Base Sequence; Carcinoma, Hepatocellular; DNA, Complementary; Human; Molecular Sequence Data; Oligonucleotides, Antisense; RNA, Messenger; Support, Non-U.S. Gov't; Translation, Genetic; Tumor Cells, Cultured
Publisher
Oxford University Press
Type
journal article

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