Liver Cancer
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Sep 15, 2003; 9(9): 1954-1958
Published online Sep 15, 2003. doi: 10.3748/wjg.v9.i9.1954
Study on relationship between expression level and molecular conformations of gene drugs targeting to hepatoma cells in vitro
Dong-Ye Yang, Fang-Gen Lu, Xi-Xiang Tang, Shui-Ping Zhao, Chun-Hui Ouyang, Xiao-Ping Wu, Xiao-Wei Liu, Xiao-Ying Wu
Dong-Ye Yang, Fang-Gen Lu, Xi-Xiang Tang, Chun-Hui Ouyang, Xiao-Ping Wu, Xiao-Wei Liu, Department of Gastroenterology, Xiangya Second Hospital, Central South University, Changsha 410011 & Institute of Sheng Life Gene Drugs, Changsha 410003, Hunan, China Shui-Ping Zhao, Department of Cardiovascularology, Xiangya Second Hospital, Central South University, Changsha 410011, Hunan, China
Xiao-Ying Wu, Department of Electron Microscope, Xiangya Medical School, Central South University, Changsha 410011, Hunan, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No. 39570355 & Hunan Health Bureau Foundation, No. Y02-038
Correspondence to: Dr. Fang-Gen Lu, Department of Gastroenterology, Xiangya Second Hospital, Central South University, Changsha 410011, Hunan Province, China. irisyang89@hotmail.com
Telephone: +86-731-4456022 Fax: +86-731-4806490
Received: July 1, 2002
Revised: July 12, 2002
Accepted: July 22, 2002
Published online: September 15, 2003
Abstract

AIM: To increase exogenous gene expression level by modulating molecular conformations of targeting gene drugs.

METHODS: The full length cDNAs of both P40 and P35 subunits of human interleukin 12 were amplified through polymerase chain reaction (PCR) and cloned into eukaryotic expressing vectors pcDNA3.1 (±) to construct plasmids of P (+)/IL-12, P (+)/P40 and P (-)/P35. These plasmids were combined with ASOR-PLL to form two targeting gene drugs [ASOR-PLL-P (+)/IL-12 and ASOR-PLL-P (+)/P40 + ASOR-PLL-P (-)/P35] in optimal ratios. The conformations of these two drugs at various concentrations adjuvant were examined under electron microscope (EM) and the drugs were transfected into HepG2 (ASGr+) cells. Semi-quantitative reverse transcription polymerase chain reaction (RT-PCR) was performed with total RNA extracted from the transfected cells to determine the hIL12 mRNA transcript level. The hIL12 protein in the cultured supernatant was measured with enzyme-linked immunosorbent assay (ELISA) 48 hours after transfection.

RESULTS: Targeting gene drugs, whose structures were granular and circle-like and diameters ranged from 25 nm to 150 nm, had the highest hIL-12 expression level. The hIL-12 expression level in the group co-transfected with ASOR-PLL-P (+)/P40 and ASOR-PLL-P (-)/P35 was higher than that of ASOR-PLL-P (+)/IL-12 transfected group.

CONCLUSION: The molecular conformations of targeting gene drugs play an important role in exogenous gene expression level, the best structures are granular and circle-like and their diameters range from 25 nm to 150 nm. The sizes and linking styles of exogenous genes also have some effects on their expression level.

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