共 44 条
Synthesis of antisense oligonucleotide-peptide conjugate targeting to GLUT-1 in HepG-2 and MCF-7 cells
被引:27
作者:

Chen, CP
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机构: Peking Univ, Sch Pharmaceut Sci, Beijing 100083, Peoples R China

Li, XX
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机构: Peking Univ, Sch Pharmaceut Sci, Beijing 100083, Peoples R China

Zhang, LR
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机构: Peking Univ, Sch Pharmaceut Sci, Beijing 100083, Peoples R China

Min, JM
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机构: Peking Univ, Sch Pharmaceut Sci, Beijing 100083, Peoples R China

Chan, JYW
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机构: Peking Univ, Sch Pharmaceut Sci, Beijing 100083, Peoples R China

Fung, KP
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机构: Peking Univ, Sch Pharmaceut Sci, Beijing 100083, Peoples R China

Wang, SQ
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机构: Peking Univ, Sch Pharmaceut Sci, Beijing 100083, Peoples R China

Zhang, LH
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机构:
Peking Univ, Sch Pharmaceut Sci, Beijing 100083, Peoples R China Peking Univ, Sch Pharmaceut Sci, Beijing 100083, Peoples R China
机构:
[1] Peking Univ, Sch Pharmaceut Sci, Beijing 100083, Peoples R China
[2] Chinese Univ Hong Kong, Dept Biochem, Shatin, Hong Kong, Peoples R China
[3] Beijing Inst Radiat Med, Beijing 100850, Peoples R China
关键词:
D O I:
10.1021/bc015540f
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
A simple procedure for the preparation of oligonucleotide-peptide conjugate was developed. p-Hydroxybenzoic acid was used as a linker for the connection of the fragments of peptide and oligonucleotide. It was found that such formed linkage was stable under the conditions of conjugate synthesis. The designed conjugate targeting to GLUT-1 showed up to 50% inhibition of cell proliferation in HepG-2 and MCF-7 cells. Comparing to the results from the expressed antisense RNA in cancer cells, it was proposed that the conjugate of signal peptide mimic and antisense oligonucleotide could improve the permeability of antisense oligonucleotide through cell membrane.
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页码:525 / 529
页数:5
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