Lin S.-B.Huang S.-S.Choo K.-B.PEI-JER CHENAu L.-C.2021-07-032021-07-0319950021-924Xhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0029013336&doi=10.1093%2foxfordjournals.jbchem.a124813&partnerID=40&md5=6eb9353d59119e3ab69446bcf044675chttps://scholars.lib.ntu.edu.tw/handle/123456789/568881α-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.Antisense oligonucleotide; Chimeric; Hepatoma cell line; Inhibition of translation; α-fetoprotein[SDGs]SDG3albumin; 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, Culturedjournal article10.1093/oxfordjournals.jbchem.a12481385866262-s2.0-0029013336