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Construction of an allosteric trans-maxizyme targeting for two distinct oncogenes
Author(s) -
Mayu Iyo,
Hiroaki Kawasaki,
Kazunari Taira
Publication year - 2002
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/2.1.115
Subject(s) - cleave , ribozyme , cancer cell , gene , cell cycle , biology , allosteric regulation , cancer , microbiology and biotechnology , rna , cancer research , genetics , dna , receptor
A maxizyme is dimmer of minimized ribozymes (minizymes) and can specifically cleave two target sites. The maxizyme also can allosterically cleave the target RNA only when it recognizes two target sites. In this study, for a cancer gene therapy, we focused two distinct oncogenes, cyclinD1 and hst-1, which are overexpressed in breast cancer cells. If we use conventional ribozymes for suppression of expression of those genes, these ribozymes affect not only these mRNAs in cancer cells but also those in normal cells because those genes are necessary for a growth factor-dependent signal transduction and a cell cycle in normal cells. To overcome this problem, we tried to design the trans-maxizyme that can cleave these mRNAs only in the breast cancer cells.

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