慢病毒载体表达CD44的工程化间充质干细胞作为结肠癌小鼠模型的候选靶向组织

Q4 Medicine
A. Nabizadeh, M. Ravanshad
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引用次数: 0

摘要

更有效地提高结肠癌细胞模型的植入和靶向性。材料与方法:在慢病毒载体上设计CD44基因的结构,并与辅助质粒PSPAX2和PMDG2一起转染到HEK293T细胞系。以优化的时间间隔收集含病毒细胞的生长培养基,追踪其转导成小鼠间充质干细胞、注射小鼠和归巢过程。结果:慢病毒载体的成功制备和转导后相应因子的适当表达可有效改善MSC在癌细胞中的归巢。结果:根据这些发现,提示CD44v6因子的高表达可有效改善肿瘤细胞的着床过程和靶向治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Engineered Mesenchymal Stem Cell by Lentiviral Vector Expressing CD44 as a Candidate to Target Colon Cancer Tissue in Mice Model
more effectively improve the implantation and targeting of the colon cancer cell model. Materials & Methods: In this study, the structure of the CD44 gene was designed in lentiviral vectors and transfected to the HEK293T cell line along with auxiliary plasmids PSPAX2 and PMDG2. The growth medium of virus-containing cells was collected at optimized intervals, and transduction into mice mesenchymal stem cells, injection into mice, and homing processes were traced. Findings: Successful production of lentiviral vectors and proper expression of the corresponding factor after transduction were effective in improving the MSC homing in cancer cell. Findings: According to these findings, it could be suggested that high expression of CD44v6 factor could be effective in improving the implantation process in cancer cells and targeting treatment.
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
20
审稿时长
6 weeks
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