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Aptamers Selected to Postoperative Lung Adenocarcinoma Detect Circulating Tumor Cells in Human Blood
Authors:Galina S Zamay  Olga S Kolovskaya  Tatiana N Zamay  Yury E Glazyrin  Alexey V Krat  Olga Zubkova  Ekaterina Spivak  Mohammed Wehbe  Ana Gargaun  Darija Muharemagic  Mariia Komarova  Valentina Grigorieva  Andrey Savchenko  Andrey A Modestov  Maxim V Berezovski  Anna S Zamay
Institution:1Krasnoyarsk State Medical University named after prof V.F. Voino-Yasenetsky, Krasnoyarsk, Russia;2Krasnoyarsk Research Center, Siberian Branch Russian Academy of Sciences, Krasnoyarsk, Russia;3Siberian Federal University, Krasnoyarsk, Russia;4Krasnoyarsk Regional Clinical Cancer Center named after A.I. Kryzhanovsky, Krasnoyarsk, Russia;5Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario, Canada
Abstract:Circulating tumor cells (CTCs) are rare cells and valuable clinical markers of prognosis of metastasis formation and prediction of patient survival. Most CTC analyses are based on the antibody-based detection of a few epithelial markers; therefore miss an important portion of mesenchymal cancer cells circulating in blood. In this work, we selected and identified DNA aptamers as specific affinity probes that bind to lung adenocarcinoma cells derived from postoperative tissues. The unique feature of our selection strategy is that aptamers are produced for lung cancer cell biomarkers in their native state and conformation without previous knowledge of the biomarkers. The aptamers did not bind to normal lung cells and lymphocytes, and had very low affinity to A549 lung adenocarcinoma culture. We applied these aptamers to detect CTCs, apoptotic bodies, and microemboli in clinical samples of peripheral blood of lung cancer and metastatic lung cancer patients. We identified aptamer-associated protein biomarkers for lung cancer such as vimentin, annexin A2, annexin A5, histone 2B, neutrophil defensin, and clusterin. Tumor-specific aptamers can be produced for individual patients and synthesized many times during anticancer therapy, thereby opening up the possibility of personalized diagnostics.
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