Line 34: | Line 34: | ||
<figure class="fig-nonfloat" style="width:100%;"> | <figure class="fig-nonfloat" style="width:100%;"> | ||
<img src="https://static.igem.org/mediawiki/2017/a/ab/T--ETH_Zurich--description_ideal.png"> | <img src="https://static.igem.org/mediawiki/2017/a/ab/T--ETH_Zurich--description_ideal.png"> | ||
− | <figcaption>Figure 1. Features of ideal bacterial cancer therapeutic as implemented into our design. <span class="bacterium">E. coli</span> Nissle inherently finds and colonizes tumors. Once in this special surrounding, it is designed to recognize the environment (1. | + | <figcaption>Figure 1. Features of ideal bacterial cancer therapeutic as implemented into our design. <span class="bacterium">E. coli</span> Nissle inherently finds and colonizes tumors. Once in this special surrounding, it is designed to recognize the environment (1. Environmental sensing), produce an MRI contrast agent (2. External detectabilty) and accummulate a cytotoxic agent it will later deliver. After confirmation of the correct colonization done by a physician, an external signal is sent via focused ultrasound (3. Response to external signal). This leads to selective delivery of the cytotoxic agent to the tumor (4. Selective cytotoxicity). </figcaption> |
</figure> | </figure> | ||
Revision as of 16:46, 29 October 2017
The ideal bacterial cancer therapeutic should be: CATE, the cancer-targeting E. coli that we have engineered, represents our vision of the ideal bacterial cancer therapeutic. With the combination of autonomous targeting, visualization and externally controlled toxin release, we believe our project provides a novel non-invasive, quick and safe approach to treating cancer (Figure 1). We decided to work with the probiotic E. coli Nissle 1917, due to its inherent tumor targeting capabilities and lack of pathogenicity, which make it the ideal chassis for development of precisely controllable features that we decided to integrate into the therapeutic. [2][3]Description
Introduction
References