| Literature DB >> 31141341 |
Wen Zhong1, Ying Pu1, Weihong Tan2, Jun Liu1, Jie Liao1, Bo Liu1, Ke Chen1, Bo Yu1, Yalan Hu1, Yuanyuan Deng1, Jiani Zhang1, Huixia Liu1.
Abstract
Aptamers, short DNA or RNA oligonucleotides, which evolved from systematic evolution of ligands by exponential enrichment (SELEX), can perform specific target recognition. Papillary thyroid carcinoma (PTC) is of high incidence worldwide, and the prognosis of advanced PTC is poor. Up to now, there is no specific biomarker that can identify PTC and defects still remain in existing diagnostic methods. Here we report an aptamer, termed TC-6, which is generated from tissue-SELEX by using sections of papillary thyroid carcinoma and a normal thyroid gland. TC-6 could specifically target intracellular components of papillary thyroid cells with high affinity ( Kd = 57.66 ± 5.93 nmol/L) and have performed excellent biocompatibility both in vivo and in vitro. Moreover, fluorescence imaging of PTC tumor-bearing mice revealed that TC-6 was able to accumulate in tumor sites and could distinguish thyroid carcinoma from other benign thyroid diseases efficiently. In addition, TC-6d, a truncated aptamer of TC-6, maintained its affinity toward PTC with Kd of 39.20 ± 8.20 nmol/L. Overall, these results indicate that TC-6 is a potential candidate for developing novel tools for diagnosis and targeted therapy of PTC.Entities:
Year: 2019 PMID: 31141341 DOI: 10.1021/acs.analchem.9b01000
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986