TY - JOUR
T1 - Stem cell tracking
T2 - Toward clinical application in oncology?
AU - Mangoni, Monica
AU - Livi, Lorenzo
AU - Biti, Giampaolo
AU - Di Cataldo, Vanessa
AU - Capaccioli, Neri
AU - Castier, Yves
AU - Loriot, Yohann
AU - Mordant, Pierre
AU - Deutsch, Eric
PY - 2012/1/1
Y1 - 2012/1/1
N2 - Noninvasive cellular imaging allows the tracking of grafted cells as well as the monitoring of their migration, suggesting potential applications to track both cancer and therapeutic stem cells. Cell tracking can be performed by two approaches: direct labeling (cells are labeled with tags) and indirect labeling (cells are transfected with a reporter gene and visualized after administration of a reporter probe). Techniques for in vivo detection of grafted cells include optic imaging, nuclear medicine imaging, magnetic resonance imaging, microCT imaging and ultrasound imaging. The ideal imaging modality would bring together high sensitivity, high resolution and low toxicity. All of the available imaging methods are based on different principles, have different properties and different limitations, so several of them can be considered complementary. Transfer of these preclinical cellular imaging modalities to stem cells has already been reported, and transfer to clinical practice within the next years can be reasonably considered.
AB - Noninvasive cellular imaging allows the tracking of grafted cells as well as the monitoring of their migration, suggesting potential applications to track both cancer and therapeutic stem cells. Cell tracking can be performed by two approaches: direct labeling (cells are labeled with tags) and indirect labeling (cells are transfected with a reporter gene and visualized after administration of a reporter probe). Techniques for in vivo detection of grafted cells include optic imaging, nuclear medicine imaging, magnetic resonance imaging, microCT imaging and ultrasound imaging. The ideal imaging modality would bring together high sensitivity, high resolution and low toxicity. All of the available imaging methods are based on different principles, have different properties and different limitations, so several of them can be considered complementary. Transfer of these preclinical cellular imaging modalities to stem cells has already been reported, and transfer to clinical practice within the next years can be reasonably considered.
KW - Cancer stem cells
KW - Cell tracking
KW - Therapeutic stem cells
UR - http://www.scopus.com/inward/record.url?scp=84872074117&partnerID=8YFLogxK
U2 - 10.1177/030089161209800501
DO - 10.1177/030089161209800501
M3 - Review article
C2 - 23235746
AN - SCOPUS:84872074117
SN - 0300-8916
VL - 98
SP - 535
EP - 542
JO - Tumori
JF - Tumori
IS - 5
ER -