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Article Open Access

A DNA aptamer recognizing MMP14 for in vivo and in vitro imaging identified by cell‑SELEX

  • Authors:
    • Xufang Huang
    • Jinman Zhong
    • Jing Ren
    • Didi Wen
    • Weiwei Zhao
    • Yi Huan
  • View Affiliations / Copyright

    Affiliations: Department of Radiology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, P.R. China
    Copyright: © Huang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 265-274
    |
    Published online on: April 25, 2019
       https://doi.org/10.3892/ol.2019.10282
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Abstract

A key challenge for the management of various types of cancer, including pancreatic cancer and hepatocellular carcinoma, is accurate diagnosis at an early stage. Matrix metalloproteinase 14 (MMP14) is overexpressed in numerous types of cancer and is associated with poor prognosis. Therefore, MMP14‑specific imaging probes have potential use in the diagnosis of MMP14‑positive cancer. Aptamers are short oligonucleotide sequences that can bind to molecular targets with a high specificity and affinity. Aptamers are typically obtained from an in vitro library; this process is usually termed systematic evolution of ligands by exponential enrichment (SELEX). In the present study, a DNA aptamer targeting MMP14 was obtained by cell‑SELEX and termed M17, which specifically recognizes MMP14‑positive cells. Aptamer M17 selectively binds to membrane proteins of MMP14‑transfected 293T cells (Kd, 4.98±1.26  nM). Pancreatic cancer cell imaging suggested that aptamer M17 can bind to the cell membranes of two pancreatic cancer cell lines (MIA PaCa‑2 and PANC‑1). In vivo tumor imaging demonstrated that the targeting recognition of MIA PaCa‑2 tumor cells in mice could be visualized using Cy5‑labeled aptamer M17. Aptamer M17‑conjugated polyethylene glycol‑Fe3O4 can specifically bind to MIA PaCa‑2 and PANC‑1 cells, and reduce MRI T2‑weighted imaging signal intensity. The DNA aptamer M17 has the advantages of simplicity of synthesis, small size, low immunogenicity, high penetrability and high affinity. Therefore, aptamer M17 is a potential molecular probe for the diagnosis and treatment of MMP14‑positive cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Huang X, Zhong J, Ren J, Wen D, Zhao W and Huan Y: A DNA aptamer recognizing MMP14 for in vivo and in vitro imaging identified by cell‑SELEX. Oncol Lett 18: 265-274, 2019.
APA
Huang, X., Zhong, J., Ren, J., Wen, D., Zhao, W., & Huan, Y. (2019). A DNA aptamer recognizing MMP14 for in vivo and in vitro imaging identified by cell‑SELEX. Oncology Letters, 18, 265-274. https://doi.org/10.3892/ol.2019.10282
MLA
Huang, X., Zhong, J., Ren, J., Wen, D., Zhao, W., Huan, Y."A DNA aptamer recognizing MMP14 for in vivo and in vitro imaging identified by cell‑SELEX". Oncology Letters 18.1 (2019): 265-274.
Chicago
Huang, X., Zhong, J., Ren, J., Wen, D., Zhao, W., Huan, Y."A DNA aptamer recognizing MMP14 for in vivo and in vitro imaging identified by cell‑SELEX". Oncology Letters 18, no. 1 (2019): 265-274. https://doi.org/10.3892/ol.2019.10282
Copy and paste a formatted citation
x
Spandidos Publications style
Huang X, Zhong J, Ren J, Wen D, Zhao W and Huan Y: A DNA aptamer recognizing MMP14 for in vivo and in vitro imaging identified by cell‑SELEX. Oncol Lett 18: 265-274, 2019.
APA
Huang, X., Zhong, J., Ren, J., Wen, D., Zhao, W., & Huan, Y. (2019). A DNA aptamer recognizing MMP14 for in vivo and in vitro imaging identified by cell‑SELEX. Oncology Letters, 18, 265-274. https://doi.org/10.3892/ol.2019.10282
MLA
Huang, X., Zhong, J., Ren, J., Wen, D., Zhao, W., Huan, Y."A DNA aptamer recognizing MMP14 for in vivo and in vitro imaging identified by cell‑SELEX". Oncology Letters 18.1 (2019): 265-274.
Chicago
Huang, X., Zhong, J., Ren, J., Wen, D., Zhao, W., Huan, Y."A DNA aptamer recognizing MMP14 for in vivo and in vitro imaging identified by cell‑SELEX". Oncology Letters 18, no. 1 (2019): 265-274. https://doi.org/10.3892/ol.2019.10282
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