Difference between revisions of "Team:SZU China/Result"
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<p class="blog-post-meta">January 1, 2014 by <a href="#">Mark</a></p> | <p class="blog-post-meta">January 1, 2014 by <a href="#">Mark</a></p> | ||
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<p>hTERT and hUPII promoters are cancer specific promoter and bladder specific promoter, respectively. By combining the two promoters into the design, we supposed that the constructed circuits have the ability to selectively identify bladder cancer cells, in which telomerase and uroplakins are both expressed.<br> | <p>hTERT and hUPII promoters are cancer specific promoter and bladder specific promoter, respectively. By combining the two promoters into the design, we supposed that the constructed circuits have the ability to selectively identify bladder cancer cells, in which telomerase and uroplakins are both expressed.<br> | ||
Revision as of 12:23, 18 September 2015
Result
Renilla Luciferase assay in three plasmids system
Three recombinant plasmids were generated and transiently transfected into a human bladder cancer cell line T24.
To test the working efficiency of our orthogonal system, we devided the cells into two groups. One has Ack in the culture medium and another does not.
Luciferase assays were performed using luminometer. Since Ack is essential for our system, we speculated that Renilla Luciferase(Rluc), the output gene in the circuits can be selectively expressed in Experiment group with Ack. As shown in Fig. 1, the activity of Renilla Luciferase(RLUC) varied widely between the two groups, and the circuit only demonstrated significant activity in the experimental group as expected. Therefore, our orthogonal system is verified to be in good condition and can work efficiently.
Luciferase assay in two plasmids system
hTERT and hUPII promoters are cancer specific promoter and bladder specific promoter, respectively. By combining the two promoters into the design, we supposed that the constructed circuits have the ability to selectively identify bladder cancer cells, in which telomerase and uroplakins are both expressed.
To test this hypothesis, we used the luciferase reporter gene as the output of the circuit and tested the luciferase activity in HFC, which is short for human fiber epithelial cell, Hela, a cervical carcinoma cell line and 5637, a bladder cancer cell line. Also, we reconstructed our system in two plasmids to test if two plasmids system can perform higher efficiency.
The result (Fig.2) shows that the activity of LUC in 5637 with Ack was about two times as high as that in 5637 without Ack and three times as high as that in Hela, while it could not be measured in HFC. We can learn from this result that this system is perfectly safe for normal cells, with no luciferase being detected in HFC. However, compared with three plasmids system, whose RLUC activity of experimental group is about 7 times as high as that of control group, the working efficiency of our orthogonal system in two plasmids is much lower. So we had better construct our system in two plasmids to express higher level of therapeutic gene in bladder cancer cells and reduce its expression in other cell types to increase its specificity.
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