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efficacious anticancer therapy. The gene therapy appears to be the most effective strategy for metastasis remission without dangerous side effects, which are common disadvantages in the case of both radioand chemotherapy. Use of bare DNA particles is very inefficient, therefore new DNA delivery system is needed. The most common vectors used in genetic therapy are genetically altered
viruses. However they generate problems that have not been solved yet. An integration into the host genome may lead to unpredictable sideeffects and increases cancer risk. Moreover this type of vector could cause acute immune response or symptoms of viral infection. Artificial systems of DNA or RNA delivery such as liposomes or alkaline polymers are characterized by low effectiveness and high toxicity.Team:Warsaw/Project/introduction
From 2009.igem.org
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==Aims of the project== | ==Aims of the project== | ||
| - | One of the most important challenges in the field of modern medicine is to invent the | + | <div class="text">One of the most important challenges in the field of modern medicine is to invent the |
efficacious anticancer therapy. The gene therapy appears to be the most effective strategy for | efficacious anticancer therapy. The gene therapy appears to be the most effective strategy for | ||
metastasis remission without dangerous side effects, which are common disadvantages in the case | metastasis remission without dangerous side effects, which are common disadvantages in the case | ||
of both radioand chemotherapy. Use of bare DNA particles is very inefficient, therefore new DNA | of both radioand chemotherapy. Use of bare DNA particles is very inefficient, therefore new DNA | ||
delivery system is needed. The most common vectors used in genetic therapy are genetically altered | delivery system is needed. The most common vectors used in genetic therapy are genetically altered | ||
| - | viruses. However they generate problems that have not been solved yet. An integration into the host genome may lead to unpredictable sideeffects and increases cancer risk. Moreover this type of vector could cause acute immune response or symptoms of viral infection. Artificial systems of DNA or RNA delivery such as liposomes or alkaline polymers are characterized by low effectiveness and high toxicity. | + | viruses. However they generate problems that have not been solved yet. An integration into the host genome may lead to unpredictable sideeffects and increases cancer risk. Moreover this type of vector could cause acute immune response or symptoms of viral infection. Artificial systems of DNA or RNA delivery such as liposomes or alkaline polymers are characterized by low effectiveness and high toxicity.</div> |
| - | The main aim of this project is to design a model system based on genetically modified | + | <div class="text">The main aim of this project is to design a model system based on genetically modified |
''Escherichia coli'' bacteria able to invade eukaryotic cells. This approach is the new alternative for | ''Escherichia coli'' bacteria able to invade eukaryotic cells. This approach is the new alternative for | ||
established for years techniques. It has most of advantages of previously known viral vectors and, | established for years techniques. It has most of advantages of previously known viral vectors and, | ||
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delivery in scientific or therapeutic approaches. The second strategy is to induce apoptosis of tumor | delivery in scientific or therapeutic approaches. The second strategy is to induce apoptosis of tumor | ||
cells by means of the proapoptotic proteins secreted to the cytoplasm by bacteria that exist within | cells by means of the proapoptotic proteins secreted to the cytoplasm by bacteria that exist within | ||
| - | the cell. | + | the cell.</div> |
{{WarFoot1}} | {{WarFoot1}} | ||
Revision as of 21:36, 21 July 2009
Aims of the project
One of the most important challenges in the field of modern medicine is to invent the
The main aim of this project is to design a model system based on genetically modified
Escherichia coli bacteria able to invade eukaryotic cells. This approach is the new alternative for established for years techniques. It has most of advantages of previously known viral vectors and, importantly, it does not induce negative changes in the patient’s genome. The created bacterial system will be applied to two problems. The first one is to create special bacterial strain, which is able to conjugate with the mitochondrion within the cytoplasm. It will enable effective DNA delivery in scientific or therapeutic approaches. The second strategy is to induce apoptosis of tumor cells by means of the proapoptotic proteins secreted to the cytoplasm by bacteria that exist within
the cell.
