Aptamers evolved from live cells as effective molecular probes for cancer study

Dihua Shangguan(Interface (United States)), Ying Li(UF Health Shands Hospital), Zhiwen Tang(Interface (United States)), Zehui Cao(Interface (United States)), Hui William Chen(Interface (United States)), Prabodhika Mallikaratchy(Interface (United States)), Kwame Sefah(Interface (United States)), Chaoyong Yang(Interface (United States)), Weihong Tan(Interface (United States))
Proceedings of the National Academy of Sciences
July 27, 2006
Cited by 1,504Open Access
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Abstract

Using cell-based aptamer selection, we have developed a strategy to use the differences at the molecular level between any two types of cells for the identification of molecular signatures on the surface of targeted cells. A group of aptamers have been generated for the specific recognition of leukemia cells. The selected aptamers can bind to target cells with an equilibrium dissociation constant (K(d)) in the nanomolar-to-picomolar range. The cell-based selection process is simple, fast, straightforward, and reproducible, and, most importantly, can be done without prior knowledge of target molecules. The selected aptamers can specifically recognize target leukemia cells mixed with normal human bone marrow aspirates and can also identify cancer cells closely related to the target cell line in real clinical specimens. The cell-based aptamer selection holds a great promise in developing specific molecular probes for cancer diagnosis and cancer biomarker discovery.


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