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A Toolbox of Genetically Engineered E.coil for Precise Targeting and Programmable Elimination of Cancer Cells According to Their Mirna Profile

机译:根据其miRNA谱进行遗传工程e.coil的工具箱,用于精确靶向和可编程消除癌细胞

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Early diagnosis and successful treatment of colorectal cancer(CRC),the second most frequent type of cancer,constitute a modern medical challenge.iGEM Greece 2017,an interdisciplinary group of undergraduate students and the very first collegiate team from Greece to take part in the worldwide iGEM competition,aims to design a toolbox that integrates miJRNA profile data and the natural propensity of bacteria to colonize cancer tissue,in order to engineer a novel probiotic anti-cancer programmable agent.By modifying the adhesion systems of E.coli(fim genes coding for the type I pili)to achieve selective binding toneoplastic cells with the simultaneous utilization of quorum sensing-based regulatory systems for their propagation in the tumor microenvironment,bacterial invasion into the cancer cells can be achieved via the expression of invasin and listeriolysin O.The end goal is the subsequent transfer of the bacterial genetic load,an RNAi-based synthetic logic circuit that is constructed according to the miRNA differential expression pattern of the cancer tissue and drives cancer cells into apoptosis through RNA interference.The aim of this study is to set the computational basis of the project by utilizing a bioinformatic analysis to identify miRNA differential expression profiles in colorectal cancer and modeling the quorum sensing behavior of the engineered strain while finalizing ongoing work in the wet lab.Experimental results regarding the transformation and efficiency of our bacterial system are expected to be available by the time of the conference due to the competitionas deadlines that we work under.
机译:早期诊断和成功治疗结直肠癌(CRC),第二种最常见的癌症类型,构成了现代医学挑战。2017年希腊,一个跨学科的本科生群体和来自希腊的第一个大学团队参加全世界IGEM竞争,旨在设计一个整合Mi​​jrna简介数据和细菌的自然倾向的工具箱,以殖民化癌组织,以工程师设计一种新型益生菌抗癌可编程剂。修饰大肠杆菌的粘附系统(FIM基因编码对于I型PILI)以实现具有基于仲裁感测的调节系统的选择性结合间质量细胞,以便在肿瘤微环境中的繁殖中,通过表达侵入素和historiolysin O.的表达可以实现细菌侵入癌细胞最终目标是随后转移细菌遗传负荷,其基于RNAI的合成逻辑电路构造了AC通过RNA干扰将癌症组织的miRNA差异表达模式传递给MiRNA差异表达模式并将癌细胞驱动到凋亡中。本研究的目的是通过利用生物信息分析来确定项目的计算基础,以鉴定结直肠癌中的miRNA差异表达谱在最终确定潮湿的实验室中的持续工作的同时建模探测菌条的批量传感行为。关于我们的细菌系统的转化和效率的实验结果将在会议上提供我们工作的比赛截止日期。

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