2016
DOI: 10.1016/j.bios.2016.01.031
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Evolution of DNA aptamers for malignant brain tumor gliosarcoma cell recognition and clinical tissue imaging

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Cited by 35 publications
(19 citation statements)
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“…Compared with other ligands, aptamers have several attractive features, including diverse structure, high specificity, high stability, rapid tissue penetration, no immunogenicity, and easy synthesis and modification. [26][27][28][29] Molecular probes loaded with specific aptamers can specifically gather in target tissues and achieve molecular imaging of target tissues. 15,30 This study prepared targeted lipid nanobubbles loaded with CAIX aptamer, explored their specific binding ability, and targeted imaging ability in various tumors, and further investigated the morphological basis of USMI in vivo.…”
Section: Introductionmentioning
confidence: 99%
“…Compared with other ligands, aptamers have several attractive features, including diverse structure, high specificity, high stability, rapid tissue penetration, no immunogenicity, and easy synthesis and modification. [26][27][28][29] Molecular probes loaded with specific aptamers can specifically gather in target tissues and achieve molecular imaging of target tissues. 15,30 This study prepared targeted lipid nanobubbles loaded with CAIX aptamer, explored their specific binding ability, and targeted imaging ability in various tumors, and further investigated the morphological basis of USMI in vivo.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, among a group of DNA aptamers selected on a cell line (K308) derived from gliosarcoma, a variant of GBM, WQY-9 aptamer was capable of recognizing gliosarcoma cells and gliosarcoma tissues, differentiating gliosarcoma from GBM [93].…”
Section: Gbmmentioning
confidence: 99%
“…The absence of specific biomarkers for CSCs impedes the development of effective therapies against them. 43 Cell-SELEX was also performed against cell lines of PDAC, 44 gliosarcoma, 45 and liver, 46,47 colorectal, 48 lung, 30,49 prostate, 50 and breast cancer, 51 among others. With the aim of finding a new biomarker for the diagnosis of PDAC, Dua et al 52 carried out cell-SELEX against two target human pancreatic cell lines, Panc-1 and Capan-1, using normal human pancreatic ductal cells for negative selection.…”
Section: Cell-selex Targeting Unrevealed Receptorsmentioning
confidence: 99%