In Vivo Evaluation of Sgc8-c Aptamer as a Molecular Imaging Probe for Colon Cancer in a Mouse Xenograft Model

被引:11
作者
Arevalo, Ana Paula [1 ]
Castelli, Romina [2 ]
Ibarra, Manuel [3 ]
Crispo, Martina [1 ]
Calzada, Victoria [2 ]
机构
[1] Inst Pasteur Montevideo, Lab Anim, Biotechnol Unit, Montevideo 11400, Uruguay
[2] Univ Republica, Fac Ciencias, Ctr Invest Nucl, Area Radiofarm, Montevideo 11400, Uruguay
[3] Univ Republica, Fac Chem, Dept Pharmaceut Sci, Montevideo 11800, Uruguay
关键词
PTK7; colon adenocarcinoma; LS174T; molecular imaging; theranostics; PROTEIN-TYROSINE KINASE-7; NUCLEAR-MEDICINE; AGENTS; FLUORESCENT;
D O I
10.3390/ijms23052466
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent biotechnological applications in the field of clinical oncology led to the identification of new biomarkers as molecular targets of cancer, and to broad developments in the field of personalized medicine. Aptamers are oligonucleotides (ssDNA or RNA) that are selected to specifically recognize a molecular target with high affinity and specificity. Based on this, new horizons for their use as molecular imaging probes are being explored. The objective of this work was to evaluate the Sgc8-c aptamer conjugated with Alexa Fluor 647 fluorophore as an imaging probe in a colon tumor xenograft mouse model, with potential application in molecular imaging. In this study, the LS174T cell line was used to induce colorectal adenocarcinoma in nude mice. After confirmation of PTK7 overexpression by immunohistochemistry, in vivo studies were performed. Pharmacokinetic, in vivo and ex vivo biodistribution imaging, and a competition assay were evaluated by fluorescence imaging. In vivo visualization of the probe in the tumors was assessed two hours after aptamer probe administration, exhibiting excellent tumor-to-background ratios in biodistribution studies and high specificity in the competition test. Our results demonstrated the functionality of Scg8-c as an imaging probe for colon cancer, with potential clinical applications.
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页数:11
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