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Aptamer-based radioimmunotherapy: the feasibility and prospect in cancer therapy

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Abstract

Radioimmunotherapy (RIT) has emerged as an attractive and promising strategy for the management of malignant diseases. It has been proven to be quite effective in the treatment of numerous tumors, such as non-Hodgkin lymphoma, metastatic prostate cancer, melanoma, thyroid cancer, colon cancer and so on. The RIT currently used is mainly based on monoclonal antibodies to recognize target antigens. As antibodies are large molecules, this method of RIT has some limitations in in vivo use, such as the immunogenicity, the high costs and low efficiency of production. Aptamer is discovered and selected by SELEX technology. As specific recognizers and binders, aptamers and antibodies have such a close similarity as to be interchangeable to some extent. But, aptamers have many advantages over antibodies: higher affinity and specificity, smaller molecular weight, more easily synthesized and modified, more rapidly penetrating into tumors, higher tumor-to-blood distribution ratio and more easily to be cleared. In addition, since aptamer has almost no immunogenicity in vivo, it can be repeatedly administered. Thus, we believe that aptamer-based RIT will be a feasible and promising way to treat human cancers, and it might display better results in cancer treatment than antibody-based RIT. In conclusion, aptamer-based RIT is hopeful to become a key therapeutics in cancer radiotherapy in the near future.

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Acknowledgments

This work was supported by the National Key Technology R&D Program of China (2008BAI57B01), National Natural Science Foundation of China (81072132), and National Natural Science Funds for Young Scholar of China (30901586/C1701).

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There is no conflict of interest among the authors in this work.

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Correspondence to Keng Shen or Ding Ma.

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Li Li and Wei Wang contributed equally to this study.

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Li, L., Wang, W., Xu, X. et al. Aptamer-based radioimmunotherapy: the feasibility and prospect in cancer therapy. J Radioanal Nucl Chem 290, 453–457 (2011). https://doi.org/10.1007/s10967-011-1340-3

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  • DOI: https://doi.org/10.1007/s10967-011-1340-3

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