Speaker
Dr
Philippe Rizo
Description
Molecular imaging allows a better insight of biological mechanisms in vivo, such as
the follow-up of gene expression, drugs biodistributions, the assessment of
therapies, and can be used for a wide variety of applications, such as cancer,
cardiovascular diseases, inflammation…
If several techniques such as nuclear medicine (SPECT, TEP), molecular resonance
imaging (MRI) and X ray computed tomography (CT) already bring information in vivo,
the optical range of interactions between light and tissues has started to be fully
exploited more recently. The advantages of the optical methods lie in their low
cost, low manipulation constraints (no radioactivity), short acquisition times and
high sensitivity. As new optical imaging techniques such as bioluminescence and
fluorescence tomography emerge and appear as new modalities to assess biological
events in small animals, the need for suitable optical probes arises.
We will present new molecular probes for fluorescence in vivo imaging of tumours in
mice. The core of these probes is constituted by a cyclodecapeptide vector, the RAFT
molecule, which has a nearly planar conformation. Both a luminescent reporter for
imaging and eventually a drug can be grafted on one face of the RAFT, while the
other can be independently functionalized by four biological ligands for tumour
targeting1. We chose to use the cRGD peptide that allows targeting of the V3
integrin receptors of the endothelium tumour cells.
The imaging function can be a classical fluorescent dye, such as Cy5, or a more
sophisticated activatable fluorescent function. For these activatable probes, the
fluorescence signal is inhibited until the probe has been internalized in the
targeted cells. Image contrast is thus dramatically improved. Examples of specific
in vivo imaging of internal tumours in nude mice bearing IGROV1 metastatic nodes
(human ovarian cancer) will be presented using the different classical and
activatable fluorescent probes as contrast agents.
1. D. Boturyn, J.L. Coll, E. Garanger, M. C. Favrot, P. Dumy, J. Am. Chem. Soc.
2004, 126(18), 5730-5739.
Author
Mrs
Isabelle Texier
(CEA Grenoble)
Co-authors
Dr
Didier Boturyn
(LEDSS, UMR CNRS 5616)
Dr
Jean-Luc Coll
(INSERM U578, Institut Albert Bonniot)
Prof.
Pascal Dumy
(LEDSS, UMR CNRS 5616)
Dr
Véronique Josserand
(ANIMAGE)
Dr
Zhahoui Jin
(INSERM U578, Institut Albert Bonniot)
Dr
jesus Razkin
(LEDSS, UMR CNRS 5616)