Team:KULeuven/Project

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(Favourite previous iGEM projects)
(A first idea: cancer treatment with genetically modified blood cells)
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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)
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)
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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)
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* 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]] 12:09, 23 May 2008 (UTC)
= Our project details=
= Our project details=

Revision as of 12:09, 23 May 2008

Home The Team Road Map The Project Parts Submitted to the Registry Modeling Notebook

Kulbanner.jpg

Contents

Project brainstorm

Favourite previous iGEM projects


Maarten Breckpot


Nathalie Busschaert


Jonas Demeulemeester

  • Virotrap Ljubljana 2007
  • 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


Benjamien Moeyaert


Stefanie Roberfroid


Hanne Tytgat


Elke Van Assche


Nick Van Damme

--> idea: solve a nice mathematical problem

--> idea: build an integrator to solve your own ODE's, also build a differentiator to make a PID-controller


Antoine Vandermeersch


Dries Vercruysse


Sigrid De Keersmaecker

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

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)

  • Sounds like a great idea! 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 (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 :) - Jonas 12:09, 23 May 2008 (UTC)

Our project details

Part 2

The Experiments

Part 3

Results