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Team:KULeuven/Project
From 2008.igem.org
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* Sounds like a great idea! [http://en.wikipedia.org/wiki/Avastin Anti-angiogenic therapy] is one of the big hopes for anti-tumor treatments. But let's keep in mind that angiogenesis (the formation of blood vessels) is only a late hallmark of tumors [http://www.google.be/url?sa=t&ct=res&cd=1&url=http%3A%2F%2Fwww.weizmann.ac.il%2Fhome%2Ffedomany%2FBioinfo05%2Flecture6_Hanahan.pdf&ei=-7E2SLbLGJCE1wblseHQDQ&usg=AFQjCNHirXaVMmdQNGl-72bk5jRva4106Q&sig2=L18rRG56VaP9wIB_mAENpA (more about these hallmarks of cancer -PDF)]. It is however a '''significant barrier''' to break through if the tumor has to grow past a certain (very limited) size. So this would be more like a therapy for later-stage malignancies, which would also be great because it's often the metastasis (the spreading of) of the tumor that is causing the more visible effects of the cancer. (pain, deterioration, ... and eventually, if untreated death). - [[user:Zeunas|Jonas]] 12:09, 23 May 2008 (UTC) | * Sounds like a great idea! [http://en.wikipedia.org/wiki/Avastin Anti-angiogenic therapy] is one of the big hopes for anti-tumor treatments. But let's keep in mind that angiogenesis (the formation of blood vessels) is only a late hallmark of tumors [http://www.google.be/url?sa=t&ct=res&cd=1&url=http%3A%2F%2Fwww.weizmann.ac.il%2Fhome%2Ffedomany%2FBioinfo05%2Flecture6_Hanahan.pdf&ei=-7E2SLbLGJCE1wblseHQDQ&usg=AFQjCNHirXaVMmdQNGl-72bk5jRva4106Q&sig2=L18rRG56VaP9wIB_mAENpA (more about these hallmarks of cancer -PDF)]. It is however a '''significant barrier''' to break through if the tumor has to grow past a certain (very limited) size. So this would be more like a therapy for later-stage malignancies, which would also be great because it's often the metastasis (the spreading of) of the tumor that is causing the more visible effects of the cancer. (pain, deterioration, ... and eventually, if untreated death). - [[user:Zeunas|Jonas]] 12:09, 23 May 2008 (UTC) | ||
| - | * Anyhow, if we proceed with this idea, it will be a challenge to get everything ready and produced in the erythrocyte (red blood cell) before it loses it's nucleus and thus also the ability to initiate ''de novo'' transcription. And to keep all this machinery silent in non-docked erythrocytes. I'm liking this challenge though :) - [[user:Zeunas|Jonas]] | + | * Anyhow, if we proceed with this idea, it will be a challenge to get everything ready and produced in the erythrocyte (red blood cell) before it loses it's nucleus and thus also the ability to initiate ''de novo'' transcription. And to keep all this machinery silent in non-docked erythrocytes. I'm liking this challenge though. Besides this has an upside as well as I feel that consequences would be less severe in this non-cell if things go awry in the system. :) - [[user:Zeunas|Jonas]] 17:30, 23 May 2008 (UTC) |
* I just thought of something that might be quite critical. If I recall correctly, there are 3 main ways in which tumors acquire blood supply. | * I just thought of something that might be quite critical. If I recall correctly, there are 3 main ways in which tumors acquire blood supply. | ||
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:# The third way to achieve blood supply is through vasculogenic mimicry, where the tumor cells actually DO line the bloodstream and mimic the normal vascular endothelium. Here tumor biomarkers should be directly displayed to the passing erythrocytes and would thus be potential targets for use in this approach. | :# The third way to achieve blood supply is through vasculogenic mimicry, where the tumor cells actually DO line the bloodstream and mimic the normal vascular endothelium. Here tumor biomarkers should be directly displayed to the passing erythrocytes and would thus be potential targets for use in this approach. | ||
| - | : OK, now for my point. In all these cases the vessels are highly abnormal, both structurally and functionally. They've got many holes, inhomogeneous bloodflow, are leaky, ... so it's very likely there will be exposed markers we can focus on but this will probably not always be the case. - [[user:zeunas|Jonas]] 14:17, 23 May 2008 (UTC) | + | : OK, now for my point. In all these cases the vessels are highly abnormal, both structurally and functionally. They've got many holes, inhomogeneous bloodflow, are leaky, ... so it's very likely there will be exposed markers we can focus on but this will probably not always be the case. So I'm really liking this idea! - [[user:zeunas|Jonas]] 14:17, 23 May 2008 (UTC) |
==A second idea: bacteria clean virusses in animals== | ==A second idea: bacteria clean virusses in animals== | ||
Revision as of 17:30, 23 May 2008
| Home | The Team | Road Map | The Project | Parts Submitted to the Registry | Modeling | Notebook |
|---|
Contents |
Project brainstorm
Favourite previous iGEM projects
Maarten Breckpot
Nathalie Busschaert
Jonas Demeulemeester
- [http://parts.mit.edu/igem07/index.php/Ljubljana Virotrap Ljubljana 2007]
- [http://parts.mit.edu/igem07/index.php/Princeton RNAi enhanced logic circuit Princeton 2007]
- Other nice parts/devices:
- Caltech: Riboswitch design for targeted cell death/molecular sensor
- Cambridge: Inducible bigger pore protein for E.coli
- Harvard: Quorum-sensing & targeting!
- Melbourne: Red/blue light responsive system through chimeric photoreceptors-kinases
- Peking U: λ-based bistable switch = very powerful
- UCSF: compartmentalization! Rewired MAPK cascade signaling through scaffolds ≅ circuit board
Andim Doldurucu
Jan Mertens
- [http://parts.mit.edu/igem07/index.php/Ljubljana Virotrap Ljubljana 2007]
- [http://parts.mit.edu/igem07/index.php/Berkeley_UC Bactoblood]
Benjamien Moeyaert
- [http://openwetware.org/wiki/IGEM:Harvard/2006/DNA_nanostructures Harvard 20006: nanostructured DNA containers]
- [http://parts.mit.edu/igem07/index.php/Berkeley_UC Bactoblood]
Stefanie Roberfroid
- [http://parts.mit.edu/igem07/index.php/Cambridge Bacteria Online]
- [http://parts.mit.edu/igem07/index.php/Berkeley_UC Bactoblood]
- [http://parts.mit.edu/igem07/index.php/Princeton RNAi enhanced logic circuit]
- some other nice ideas
- [http://parts.mit.edu/igem07/index.php/Edinburgh Self-flavouring yoghurt]
- Detection of metals: [http://parts.mit.edu/igem07/index.php/Brown Lead], [http://parts.mit.edu/igem07/index.php/Saint_Petersburg Copper]
Hanne Tytgat
- [http://parts.mit.edu/igem07/index.php/Berkeley_UC Bactoblood]
- [http://parts.mit.edu/igem07/index.php/MIT Sensing & removing Hg ions - MIT 2007]
- [http://parts.mit.edu/igem07/index.php/Imperial/Infector_Detector/Introduction Infector detector]
Elke Van Assche
- [http://parts.mit.edu/wiki/index.php/MIT_2006 Eau d'E.coli MIT 2006]
- [http://parts.mit.edu/igem07/index.php/Berkeley_UC Bactoblood Berkeley UC 2007]
- [http://parts.mit.edu/igem07/index.php/Princeton RNAi enhanced logic circuit Princeton 2007]
Nick Van Damme
- [http://parts.mit.edu/igem07/index.php/Davidson_Missouri_W Bacterial Computer]
--> idea: solve a nice mathematical problem
- several electronical/biological components to build an entire complex combinational logic system
- [http://parts.mit.edu/igem07/index.php/USTC Extensible Logic Circuit in Bacteria]: both components and linking
- [http://parts.mit.edu/igem07/index.php/Valencia Comparator]
- [http://parts.mit.edu/igem07/index.php/Bologna Schmitt trigger]
--> idea: build an integrator to solve your own ODE's, also build a differentiator to make a PID-controller
Antoine Vandermeersch
- [http://parts2.mit.edu/wiki/index.php/University_of_Texas_2006 Texas 2006: Edge Detector]
- [http://parts.mit.edu/igem07/index.php/Rice/Project_B:_Quorumtaxis Rice 2007: Quorumtaxis]
- [http://parts.mit.edu/igem07/index.php/Berkeley_LBL Berkeley LBL 2007: Solar Bacter]
Dries Vercruysse
Sigrid De Keersmaecker
- [http://parts.mit.edu/igem07/index.php/MIT Sensing & removing Hg ions - MIT 2007]
- [http://parts.mit.edu/igem07/index.php/Edinburgh Self-flavouring yoghurt - Edinburgh 2007]
- [http://parts.mit.edu/igem07/index.php/Missouri_Miners Biological Timer - Missouri Miners 2007]
- [http://parts.mit.edu/igem07/index.php/Ljubljana Virotrap - Ljubljana 2007]
- [http://parts.mit.edu/igem07/index.php/Taipei/Taipei GlucOperon - Taipei 2007]
- [http://parts.mit.edu/igem07/index.php/Berkeley_LBL Solar Bacter - Berkeley_LBL 2007]
- [http://parts.mit.edu/igem07/index.php/Berkeley_UC Bactoblood - Berkeley_UC 2007]
iGEM judging tracks
- Foundational Research - basic science and engineering research
- Information Processing - genetically encoded control, logic, and memory
- Energy - biological fuels, feedstocks, and other energy projects
- Environment- sensing bioremediation of environmental state
- Health & Medicine - applied projects with the goal of directly improving the human condition
Other
[http://openwetware.org/wiki/IGEM:Idea_exchange Idea exchange - iGEM ideas posted by other teams]
Our project
Our abstract
A first idea: cancer treatment with genetically modified blood cells
As cancer cells need a lot of energy to replicate themselves, they should be well provided with blood. Therefore, blood cells could be the right choice for in situ treatment of cancer. First, we should immobilize these blood cells on the cancer cells. Subsequently, these blood cells should secrete specific agents that reduce the activity of the cancer cells. (These 2 steps may come in handy if we want to split up in 2 subgroups)
Notes
- Sounds like a great idea! [http://en.wikipedia.org/wiki/Avastin Anti-angiogenic therapy] is one of the big hopes for anti-tumor treatments. But let's keep in mind that angiogenesis (the formation of blood vessels) is only a late hallmark of tumors [http://www.google.be/url?sa=t&ct=res&cd=1&url=http%3A%2F%2Fwww.weizmann.ac.il%2Fhome%2Ffedomany%2FBioinfo05%2Flecture6_Hanahan.pdf&ei=-7E2SLbLGJCE1wblseHQDQ&usg=AFQjCNHirXaVMmdQNGl-72bk5jRva4106Q&sig2=L18rRG56VaP9wIB_mAENpA (more about these hallmarks of cancer -PDF)]. It is however a significant barrier to break through if the tumor has to grow past a certain (very limited) size. So this would be more like a therapy for later-stage malignancies, which would also be great because it's often the metastasis (the spreading of) of the tumor that is causing the more visible effects of the cancer. (pain, deterioration, ... and eventually, if untreated death). - Jonas 12:09, 23 May 2008 (UTC)
- Anyhow, if we proceed with this idea, it will be a challenge to get everything ready and produced in the erythrocyte (red blood cell) before it loses it's nucleus and thus also the ability to initiate de novo transcription. And to keep all this machinery silent in non-docked erythrocytes. I'm liking this challenge though. Besides this has an upside as well as I feel that consequences would be less severe in this non-cell if things go awry in the system. :) - Jonas 17:30, 23 May 2008 (UTC)
- I just thought of something that might be quite critical. If I recall correctly, there are 3 main ways in which tumors acquire blood supply.
- The first one is through a recapitulation of embryonic development. This is the recruitment of vascular endothelial precursors or the activation of local endothelium via factors like VEGF (angiogenic sprouting or intussusceptive growth). In this case, the 'vessels' of the tumor blood supply are lined mostly with endothelial cells which are actually NOT malignant, but are kind of working together with the tumor cells.
- A successful cancer metastasis (a secondary tumor, derived from the original) will co-opt blood vessels and these will thus also be lined mostly with endothelium cells.
- The third way to achieve blood supply is through vasculogenic mimicry, where the tumor cells actually DO line the bloodstream and mimic the normal vascular endothelium. Here tumor biomarkers should be directly displayed to the passing erythrocytes and would thus be potential targets for use in this approach.
- OK, now for my point. In all these cases the vessels are highly abnormal, both structurally and functionally. They've got many holes, inhomogeneous bloodflow, are leaky, ... so it's very likely there will be exposed markers we can focus on but this will probably not always be the case. So I'm really liking this idea! - Jonas 14:17, 23 May 2008 (UTC)
A second idea: bacteria clean virusses in animals
This is an improvement of the idea of Ljubljana: we cannot reprogram the immune system, but we can reprogram bacteria. So, what we could do is make bacteria produce viral receptors (challenge 1) which are modified so that when a virus attaches to them, a restriction enzyme is transcribed (challenge 2). This RE degrades the viral DNA and the bacterial DNA, thus killing the bacterium. This way, the bacteria clean all virusses from the body. When this is established, we can induce a suicide signal for the bacteria (challenge 3). Big problems:
- Is it possible to make a eukaryotic virus attack a prokaryote (also a fundamental question)?
- Immunogenicity bacterium (cf. Bactoblood)! Bmoeyaert
