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Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells

Well-preserved mRNA in circulating tumor cells (CTCs) offers an ideal material for conducting molecular profiling of tumors, thereby providing a noninvasive diagnostic solution for guiding treatment intervention and monitoring disease progression. However, it is technically challenging to purify CTC...

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Autores principales: Dong, Jiantong, Jan, Yu Jen, Cheng, Ju, Zhang, Ryan Y., Meng, Meng, Smalley, Matthew, Chen, Pin-Jung, Tang, Xinghong, Tseng, Patrick, Bao, Lirong, Huang, Tzu-Yang, Zhou, Dongjing, Liu, Yupin, Chai, Xiaoshu, Zhang, Haibo, Zhou, Anqi, Agopian, Vatche G., Posadas, Edwin M., Shyue, Jing-Jong, Jonas, Steven J., Weiss, Paul S., Li, Mengyuan, Zheng, Guangjuan, Yu, Hsiao-hua, Zhao, Meiping, Tseng, Hsian-Rong, Zhu, Yazhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669017/
https://www.ncbi.nlm.nih.gov/pubmed/31392269
http://dx.doi.org/10.1126/sciadv.aav9186
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author Dong, Jiantong
Jan, Yu Jen
Cheng, Ju
Zhang, Ryan Y.
Meng, Meng
Smalley, Matthew
Chen, Pin-Jung
Tang, Xinghong
Tseng, Patrick
Bao, Lirong
Huang, Tzu-Yang
Zhou, Dongjing
Liu, Yupin
Chai, Xiaoshu
Zhang, Haibo
Zhou, Anqi
Agopian, Vatche G.
Posadas, Edwin M.
Shyue, Jing-Jong
Jonas, Steven J.
Weiss, Paul S.
Li, Mengyuan
Zheng, Guangjuan
Yu, Hsiao-hua
Zhao, Meiping
Tseng, Hsian-Rong
Zhu, Yazhen
author_facet Dong, Jiantong
Jan, Yu Jen
Cheng, Ju
Zhang, Ryan Y.
Meng, Meng
Smalley, Matthew
Chen, Pin-Jung
Tang, Xinghong
Tseng, Patrick
Bao, Lirong
Huang, Tzu-Yang
Zhou, Dongjing
Liu, Yupin
Chai, Xiaoshu
Zhang, Haibo
Zhou, Anqi
Agopian, Vatche G.
Posadas, Edwin M.
Shyue, Jing-Jong
Jonas, Steven J.
Weiss, Paul S.
Li, Mengyuan
Zheng, Guangjuan
Yu, Hsiao-hua
Zhao, Meiping
Tseng, Hsian-Rong
Zhu, Yazhen
author_sort Dong, Jiantong
collection PubMed
description Well-preserved mRNA in circulating tumor cells (CTCs) offers an ideal material for conducting molecular profiling of tumors, thereby providing a noninvasive diagnostic solution for guiding treatment intervention and monitoring disease progression. However, it is technically challenging to purify CTCs while retaining high-quality mRNA.Here, we demonstrate a covalent chemistry–based nanostructured silicon substrate (“Click Chip”) for CTC purification that leverages bioorthogonal ligation–mediated CTC capture and disulfide cleavage–driven CTC release. This platform is ideal for CTC mRNA assays because of its efficient, specific, and rapid purification of pooled CTCs, enabling downstream molecular quantification using reverse transcription Droplet Digital polymerase chain reaction. Rearrangements of ALK/ROS1 were quantified using CTC mRNA and matched with those identified in biopsy specimens from 12 patients with late-stage non–small cell lung cancer. Moreover, CTC counts and copy numbers of ALK/ROS1 rearrangements could be used together for evaluating treatment responses and disease progression.
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spelling pubmed-66690172019-08-07 Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells Dong, Jiantong Jan, Yu Jen Cheng, Ju Zhang, Ryan Y. Meng, Meng Smalley, Matthew Chen, Pin-Jung Tang, Xinghong Tseng, Patrick Bao, Lirong Huang, Tzu-Yang Zhou, Dongjing Liu, Yupin Chai, Xiaoshu Zhang, Haibo Zhou, Anqi Agopian, Vatche G. Posadas, Edwin M. Shyue, Jing-Jong Jonas, Steven J. Weiss, Paul S. Li, Mengyuan Zheng, Guangjuan Yu, Hsiao-hua Zhao, Meiping Tseng, Hsian-Rong Zhu, Yazhen Sci Adv Research Articles Well-preserved mRNA in circulating tumor cells (CTCs) offers an ideal material for conducting molecular profiling of tumors, thereby providing a noninvasive diagnostic solution for guiding treatment intervention and monitoring disease progression. However, it is technically challenging to purify CTCs while retaining high-quality mRNA.Here, we demonstrate a covalent chemistry–based nanostructured silicon substrate (“Click Chip”) for CTC purification that leverages bioorthogonal ligation–mediated CTC capture and disulfide cleavage–driven CTC release. This platform is ideal for CTC mRNA assays because of its efficient, specific, and rapid purification of pooled CTCs, enabling downstream molecular quantification using reverse transcription Droplet Digital polymerase chain reaction. Rearrangements of ALK/ROS1 were quantified using CTC mRNA and matched with those identified in biopsy specimens from 12 patients with late-stage non–small cell lung cancer. Moreover, CTC counts and copy numbers of ALK/ROS1 rearrangements could be used together for evaluating treatment responses and disease progression. American Association for the Advancement of Science 2019-07-31 /pmc/articles/PMC6669017/ /pubmed/31392269 http://dx.doi.org/10.1126/sciadv.aav9186 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Dong, Jiantong
Jan, Yu Jen
Cheng, Ju
Zhang, Ryan Y.
Meng, Meng
Smalley, Matthew
Chen, Pin-Jung
Tang, Xinghong
Tseng, Patrick
Bao, Lirong
Huang, Tzu-Yang
Zhou, Dongjing
Liu, Yupin
Chai, Xiaoshu
Zhang, Haibo
Zhou, Anqi
Agopian, Vatche G.
Posadas, Edwin M.
Shyue, Jing-Jong
Jonas, Steven J.
Weiss, Paul S.
Li, Mengyuan
Zheng, Guangjuan
Yu, Hsiao-hua
Zhao, Meiping
Tseng, Hsian-Rong
Zhu, Yazhen
Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells
title Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells
title_full Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells
title_fullStr Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells
title_full_unstemmed Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells
title_short Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells
title_sort covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669017/
https://www.ncbi.nlm.nih.gov/pubmed/31392269
http://dx.doi.org/10.1126/sciadv.aav9186
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