Abstract
Colorectal cancer (CRC) as the second leading cause of global cancer deaths poses critical challenges in clinical settings. Cancer-derived small extracellular vesicles (sEVs), which are secreted by cancer cells, have been shown to mediate tumor development, invasion, and even metastasis, and have thus received increasing attention for the development of cancer diagnostic or therapeutic platforms. In the present study, w e have developed the sEV-targeted systematic evolution of ligands by exponential enrichment (E-SELEX) method to generate a high-quality aptamer (CCE-10F) that recognizes and binds to CRC-derived sEVs. Via an in-depth investigation, w e confirmed that this novel aptamer possesses high affinity (Kd = 3.41nM) for CRC-derived sEVs and exhibits a wide linear range (2.0 × 104 - 1.0 × 106 particles/μL) with a limit of detection (LOD) of 1.0 × 103 particles/μL. Furthermore, the aptamer discriminates CRC cell-derived sEVs from those derived from normal cell, human serum, and other cancer cells, showing high specificity for CRC cell-derived sEVs and significantly suppresses the critical processes of metastasis, including cellular migration, invasion, and angiogenesis, which are originally induced by sEVs themselves. These findings are highly encouraging for the potential use of the aptamer in sEV-based diagnostic and therapeutic applications. This article is protected by copyright. All rights reserved.
Published Version
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