RT Journal Article SR Electronic T1 Radiosynthesis and evaluation of [11C]SU11274 for in vivo PET imaging of MET receptors JF Journal of Nuclear Medicine JO J Nucl Med FD Society of Nuclear Medicine SP 1121 OP 1121 VO 51 IS supplement 2 A1 Wu, Chunying A1 Tang, Zhe A1 Fan, Wenwei A1 Zhu, Wenxia A1 Wang, Changning A1 Somoza, Edurado A1 Owino, Norbert A1 Ma, Patrick A1 Wang, Yanming YR 2010 UL http://jnm.snmjournals.org/content/51/supplement_2/1121.abstract AB 1121 Objectives To radiosynthesize and evaluate a molecular imaging probe, termed [11C]SU11274 ([11C]14), for quantification of MET receptors in human cancers in vivo. Methods (3-[3,5-dimethyl-4-(4-methyl-piperazine-carbonyl)-1H-pyrrol-2-ylmethylene]-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid (3-chlorophenyl)-methyl amide (14) was radiolabelled with C-11 through radiomethylation of 3-[3,5-dimethyl-4-(piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-2-oxo-2,3-dihyro-1H-indole-5-sulfonic acid (3-chlorophenyl)-methyl amide hydrochloride (13) that was designed as the precursor. For in vivo microPET studies, two human lung cancer xenograft models were established using MET-positive NCI-H1975 and MET- negative NCI-H520. MRI (9.4T) studies were performed right after microPET to co-register with microPET images. In vitro histological studies were further conducted after microPET and MRI imaging. Results The synthesis of 13 was achieved in 10 steps with a total yield of 9.7%. [11C]14 was obtained in a range of 5-10 % radiochemical yield and over 95% radiochemical purity after HPLC preparation. Quantitative microPET study showed that the tumor uptake of the [11C]14 in the NCI-H1975 xenograft was significantly higher than that in the NCI-H520 xenograft, which is consistent with their corresponding immunohistochemical tissue staining patterns of MET receptors from the same animals. Conclusions These studies demonstrated that [11C]14-PET is an appropriate imaging marker for quantification of MET receptor in vivo and can facilitate efficacy evaluation in the clinical development of MET targeted cancer therapeutics