TY - JOUR
T1 - Magnetic resonance imaging detection of tumor cells by targeting low-density lipoprotein receptors with Gd-loaded low-density lipoprotein particles
AU - Crich, Simonetta Geninatti
AU - Lanzardo, Stefania
AU - Alberti, Diego
AU - Belfiore, Simona
AU - Ciampa, Anna
AU - Giovenzana, Giovanni B.
AU - Lovazzano, Clara
AU - Pagliarin, Roberto
AU - Aime, Silvio
N1 - Funding Information:
Abbreviations: HSA, human serum albumin; MRI, magnetic resonance imaging; LDL, low-density lipoprotein; Gd, gadolinium; LDLR, low-density lipoprotein receptor; Rdh, rhodamine-labeled phospholipid; HepG2, human hepatoblastoma G2; B16-F10, mouse melanoma; SI, signal intensity; TT, target tissue; LPDS, lipoprotein-deficient serum; NMRD, nuclear magnetic relaxation dispersion; NMR, nuclear magnetic resonance; MR, magnetic resonance; DTPA, diethylenetriaminepentaacetic acid; ICP-MS, inductively coupled plasma mass spectrometry; CMC, critical micellar concentration Address all correspondence to: Silvio Aime, Center for Molecular Imaging, University of Torino, via Nizza 52, Torino 10126, Italy. E-mail: [email protected] 1This work was supported by Ministero Istruzione Università Ricerca (Progetto Ricerca Interesse Nazionale and Fondo Inegrativo Ricerca di Base) and it has been carried out under the frame of the European Cooperation in the field of Scientific and Technical Research D38 Action, Meditrans Integrated Project, European Molecular Imaging Laboratories, and Diagnostic Molecular Imaging, European Union Network of Excellence. Support from Bracco Imaging SpA is gratefully acknowledged. Received 3 August 2007; Revised 21 September 2007; Accepted 24 September 2007.
PY - 2007/12
Y1 - 2007/12
N2 - Gd-DO3A-diph and Gd-AAZTAC17 are lipophilic magnetic resonance imaging (MRI) agents that display high affinity for low-density lipoprotein (LDL) particles. However, on binding to LDL, Gd-DO3A-diph shows a decreased hydration that results in a lower enhancement of water proton relaxation rate. Conversely, Gd-AAZTAC17 displays a strong relaxation enhancement at the imaging fields. Each LDL particle can load up to 100 and 400 UNITS of Gd-DO3A-diph and Gd-AAZTAC17, respectively. Their LDL adducts are taken up by human hepatoblastoma G2 (HepG2) and melanoma B16 tumor cells when added to the incubation medium. T1 measurements of the labeled cells indicate that Gd-AAZTAC17 is significantly more efficient than Gd-DO3A-diph. Furthermore, it has been found that HepG2 hepatoma cells can internalize higher amounts of Gd-AAZTAC17 than B16 cells and the involvement of LDL receptors (LDLRs) has been demonstrated in competition assays with free LDL. Gd-AAZTAC17/LDL adduct proved to be an efficient probe in the magnetic resonance (MR) visualization of subcutaneous tumors in animal models obtained by injecting B16 melanoma cells into the right flank of mice. Finally, confocal microscopy validation of the distribution of LDL-based probes in the tumor has been obtained by doping the Gd-AAZTAC17/LDL adduct with a fluorescent phospholipid moiety.
AB - Gd-DO3A-diph and Gd-AAZTAC17 are lipophilic magnetic resonance imaging (MRI) agents that display high affinity for low-density lipoprotein (LDL) particles. However, on binding to LDL, Gd-DO3A-diph shows a decreased hydration that results in a lower enhancement of water proton relaxation rate. Conversely, Gd-AAZTAC17 displays a strong relaxation enhancement at the imaging fields. Each LDL particle can load up to 100 and 400 UNITS of Gd-DO3A-diph and Gd-AAZTAC17, respectively. Their LDL adducts are taken up by human hepatoblastoma G2 (HepG2) and melanoma B16 tumor cells when added to the incubation medium. T1 measurements of the labeled cells indicate that Gd-AAZTAC17 is significantly more efficient than Gd-DO3A-diph. Furthermore, it has been found that HepG2 hepatoma cells can internalize higher amounts of Gd-AAZTAC17 than B16 cells and the involvement of LDL receptors (LDLRs) has been demonstrated in competition assays with free LDL. Gd-AAZTAC17/LDL adduct proved to be an efficient probe in the magnetic resonance (MR) visualization of subcutaneous tumors in animal models obtained by injecting B16 melanoma cells into the right flank of mice. Finally, confocal microscopy validation of the distribution of LDL-based probes in the tumor has been obtained by doping the Gd-AAZTAC17/LDL adduct with a fluorescent phospholipid moiety.
KW - Dual imaging probe
KW - Gd complexes
KW - LDL
KW - Magnetic resonance imaging
KW - Tumor
UR - http://www.scopus.com/inward/record.url?scp=37149042647&partnerID=8YFLogxK
U2 - 10.1593/neo.07682
DO - 10.1593/neo.07682
M3 - Article
SN - 1522-8002
VL - 9
SP - 1046
EP - 1056
JO - Neoplasia
JF - Neoplasia
IS - 12
ER -