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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Science advances 2019-07, Vol.5 (7), p.eaav9186
Hauptverfasser: 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
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 7
container_start_page eaav9186
container_title Science advances
container_volume 5
creator 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
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.
doi_str_mv 10.1126/sciadv.aav9186
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6669017</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2270010448</sourcerecordid><originalsourceid>FETCH-LOGICAL-c390t-373829a24db4a7c0c70c71f2bcb7c717e839277c74e357391bed6be7275686bc3</originalsourceid><addsrcrecordid>eNpVUU1r3DAQFaWlCWmuPRYde9mtPmzJvhTK0i8I9NKexUgeb1RsKdGHIff-8CrsNqQwME_Mm6eZeYS85WzPuVAfsvMwbXuAbeSDekEuhdT9TvTd8PIZviDXOf9mjPFOqZ6Pr8mF5HIUQo2X5M8hbrBgKNTd4upzSQ80BhogxIarKzXhRHO17QUFM8UAdmk5xODDBtlvSO8rhOJn76D41hxnesSANCGkBOGIa9PP1AfqfHJ1aaxwpKWuMVGHy5LfkFczLBmvz_mK_Pry-efh2-7mx9fvh083OydHVnZSy0GMILrJdqAdc7oFn4V1VjegcWhb6QY7lL2WI7c4KYta6F4Nyjp5RT6edO-qXXFybawEi7lLfoX0YCJ4838l-FtzjJtRSo2M6ybw_iyQ4n3FXEw72eMKEDDWbITQ7cys64ZG3Z-oLsWcE85P33BmHt0zJ_fM2b3W8O75cE_0f17Jv0WEnV8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2270010448</pqid></control><display><type>article</type><title>Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>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</creator><creatorcontrib>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</creatorcontrib><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.</description><identifier>ISSN: 2375-2548</identifier><identifier>EISSN: 2375-2548</identifier><identifier>DOI: 10.1126/sciadv.aav9186</identifier><identifier>PMID: 31392269</identifier><language>eng</language><publisher>United States: American Association for the Advancement of Science</publisher><subject>Adult ; Aged ; Anaplastic Lymphoma Kinase - chemistry ; Anaplastic Lymphoma Kinase - genetics ; Cancer ; Carcinoma, Non-Small-Cell Lung - blood ; Carcinoma, Non-Small-Cell Lung - chemistry ; Carcinoma, Non-Small-Cell Lung - genetics ; Carcinoma, Non-Small-Cell Lung - pathology ; Cell Line, Tumor ; Chemistry ; Click Chemistry - methods ; Female ; Gene Rearrangement - genetics ; Health and Medicine ; Humans ; Male ; Middle Aged ; Nanostructures - chemistry ; Neoplasm Staging ; Neoplastic Cells, Circulating - chemistry ; Protein-Tyrosine Kinases - chemistry ; Protein-Tyrosine Kinases - genetics ; Proto-Oncogene Proteins - chemistry ; Proto-Oncogene Proteins - genetics ; RNA, Messenger - blood ; RNA, Messenger - isolation &amp; purification ; SciAdv r-articles ; Silicon - chemistry</subject><ispartof>Science advances, 2019-07, Vol.5 (7), p.eaav9186</ispartof><rights>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). 2019 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-373829a24db4a7c0c70c71f2bcb7c717e839277c74e357391bed6be7275686bc3</citedby><cites>FETCH-LOGICAL-c390t-373829a24db4a7c0c70c71f2bcb7c717e839277c74e357391bed6be7275686bc3</cites><orcidid>0000-0001-5570-2470 ; 0000-0002-8696-8738 ; 0000-0002-2130-8085 ; 0000-0003-0942-5905 ; 0000-0002-3603-6932 ; 0000-0001-8649-1346 ; 0000-0002-6143-078X ; 0000-0001-7063-711X ; 0000-0002-4664-1845 ; 0000-0002-3122-4053 ; 0000-0002-6536-5647 ; 0000-0002-2962-2933 ; 0000-0002-9715-6292 ; 0000-0001-5527-6248 ; 0000-0002-8508-659X ; 0000-0001-9358-3054 ; 0000-0002-8111-0249 ; 0000-0002-2342-5058</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669017/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669017/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,27926,27927,53793,53795</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31392269$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dong, Jiantong</creatorcontrib><creatorcontrib>Jan, Yu Jen</creatorcontrib><creatorcontrib>Cheng, Ju</creatorcontrib><creatorcontrib>Zhang, Ryan Y</creatorcontrib><creatorcontrib>Meng, Meng</creatorcontrib><creatorcontrib>Smalley, Matthew</creatorcontrib><creatorcontrib>Chen, Pin-Jung</creatorcontrib><creatorcontrib>Tang, Xinghong</creatorcontrib><creatorcontrib>Tseng, Patrick</creatorcontrib><creatorcontrib>Bao, Lirong</creatorcontrib><creatorcontrib>Huang, Tzu-Yang</creatorcontrib><creatorcontrib>Zhou, Dongjing</creatorcontrib><creatorcontrib>Liu, Yupin</creatorcontrib><creatorcontrib>Chai, Xiaoshu</creatorcontrib><creatorcontrib>Zhang, Haibo</creatorcontrib><creatorcontrib>Zhou, Anqi</creatorcontrib><creatorcontrib>Agopian, Vatche G</creatorcontrib><creatorcontrib>Posadas, Edwin M</creatorcontrib><creatorcontrib>Shyue, Jing-Jong</creatorcontrib><creatorcontrib>Jonas, Steven J</creatorcontrib><creatorcontrib>Weiss, Paul S</creatorcontrib><creatorcontrib>Li, Mengyuan</creatorcontrib><creatorcontrib>Zheng, Guangjuan</creatorcontrib><creatorcontrib>Yu, Hsiao-Hua</creatorcontrib><creatorcontrib>Zhao, Meiping</creatorcontrib><creatorcontrib>Tseng, Hsian-Rong</creatorcontrib><creatorcontrib>Zhu, Yazhen</creatorcontrib><title>Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells</title><title>Science advances</title><addtitle>Sci Adv</addtitle><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.</description><subject>Adult</subject><subject>Aged</subject><subject>Anaplastic Lymphoma Kinase - chemistry</subject><subject>Anaplastic Lymphoma Kinase - genetics</subject><subject>Cancer</subject><subject>Carcinoma, Non-Small-Cell Lung - blood</subject><subject>Carcinoma, Non-Small-Cell Lung - chemistry</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Cell Line, Tumor</subject><subject>Chemistry</subject><subject>Click Chemistry - methods</subject><subject>Female</subject><subject>Gene Rearrangement - genetics</subject><subject>Health and Medicine</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nanostructures - chemistry</subject><subject>Neoplasm Staging</subject><subject>Neoplastic Cells, Circulating - chemistry</subject><subject>Protein-Tyrosine Kinases - chemistry</subject><subject>Protein-Tyrosine Kinases - genetics</subject><subject>Proto-Oncogene Proteins - chemistry</subject><subject>Proto-Oncogene Proteins - genetics</subject><subject>RNA, Messenger - blood</subject><subject>RNA, Messenger - isolation &amp; purification</subject><subject>SciAdv r-articles</subject><subject>Silicon - chemistry</subject><issn>2375-2548</issn><issn>2375-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1r3DAQFaWlCWmuPRYde9mtPmzJvhTK0i8I9NKexUgeb1RsKdGHIff-8CrsNqQwME_Mm6eZeYS85WzPuVAfsvMwbXuAbeSDekEuhdT9TvTd8PIZviDXOf9mjPFOqZ6Pr8mF5HIUQo2X5M8hbrBgKNTd4upzSQ80BhogxIarKzXhRHO17QUFM8UAdmk5xODDBtlvSO8rhOJn76D41hxnesSANCGkBOGIa9PP1AfqfHJ1aaxwpKWuMVGHy5LfkFczLBmvz_mK_Pry-efh2-7mx9fvh083OydHVnZSy0GMILrJdqAdc7oFn4V1VjegcWhb6QY7lL2WI7c4KYta6F4Nyjp5RT6edO-qXXFybawEi7lLfoX0YCJ4838l-FtzjJtRSo2M6ybw_iyQ4n3FXEw72eMKEDDWbITQ7cys64ZG3Z-oLsWcE85P33BmHt0zJ_fM2b3W8O75cE_0f17Jv0WEnV8</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Dong, Jiantong</creator><creator>Jan, Yu Jen</creator><creator>Cheng, Ju</creator><creator>Zhang, Ryan Y</creator><creator>Meng, Meng</creator><creator>Smalley, Matthew</creator><creator>Chen, Pin-Jung</creator><creator>Tang, Xinghong</creator><creator>Tseng, Patrick</creator><creator>Bao, Lirong</creator><creator>Huang, Tzu-Yang</creator><creator>Zhou, Dongjing</creator><creator>Liu, Yupin</creator><creator>Chai, Xiaoshu</creator><creator>Zhang, Haibo</creator><creator>Zhou, Anqi</creator><creator>Agopian, Vatche G</creator><creator>Posadas, Edwin M</creator><creator>Shyue, Jing-Jong</creator><creator>Jonas, Steven J</creator><creator>Weiss, Paul S</creator><creator>Li, Mengyuan</creator><creator>Zheng, Guangjuan</creator><creator>Yu, Hsiao-Hua</creator><creator>Zhao, Meiping</creator><creator>Tseng, Hsian-Rong</creator><creator>Zhu, Yazhen</creator><general>American Association for the Advancement of Science</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5570-2470</orcidid><orcidid>https://orcid.org/0000-0002-8696-8738</orcidid><orcidid>https://orcid.org/0000-0002-2130-8085</orcidid><orcidid>https://orcid.org/0000-0003-0942-5905</orcidid><orcidid>https://orcid.org/0000-0002-3603-6932</orcidid><orcidid>https://orcid.org/0000-0001-8649-1346</orcidid><orcidid>https://orcid.org/0000-0002-6143-078X</orcidid><orcidid>https://orcid.org/0000-0001-7063-711X</orcidid><orcidid>https://orcid.org/0000-0002-4664-1845</orcidid><orcidid>https://orcid.org/0000-0002-3122-4053</orcidid><orcidid>https://orcid.org/0000-0002-6536-5647</orcidid><orcidid>https://orcid.org/0000-0002-2962-2933</orcidid><orcidid>https://orcid.org/0000-0002-9715-6292</orcidid><orcidid>https://orcid.org/0000-0001-5527-6248</orcidid><orcidid>https://orcid.org/0000-0002-8508-659X</orcidid><orcidid>https://orcid.org/0000-0001-9358-3054</orcidid><orcidid>https://orcid.org/0000-0002-8111-0249</orcidid><orcidid>https://orcid.org/0000-0002-2342-5058</orcidid></search><sort><creationdate>20190701</creationdate><title>Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells</title><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-373829a24db4a7c0c70c71f2bcb7c717e839277c74e357391bed6be7275686bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Anaplastic Lymphoma Kinase - chemistry</topic><topic>Anaplastic Lymphoma Kinase - genetics</topic><topic>Cancer</topic><topic>Carcinoma, Non-Small-Cell Lung - blood</topic><topic>Carcinoma, Non-Small-Cell Lung - chemistry</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Cell Line, Tumor</topic><topic>Chemistry</topic><topic>Click Chemistry - methods</topic><topic>Female</topic><topic>Gene Rearrangement - genetics</topic><topic>Health and Medicine</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nanostructures - chemistry</topic><topic>Neoplasm Staging</topic><topic>Neoplastic Cells, Circulating - chemistry</topic><topic>Protein-Tyrosine Kinases - chemistry</topic><topic>Protein-Tyrosine Kinases - genetics</topic><topic>Proto-Oncogene Proteins - chemistry</topic><topic>Proto-Oncogene Proteins - genetics</topic><topic>RNA, Messenger - blood</topic><topic>RNA, Messenger - isolation &amp; purification</topic><topic>SciAdv r-articles</topic><topic>Silicon - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dong, Jiantong</creatorcontrib><creatorcontrib>Jan, Yu Jen</creatorcontrib><creatorcontrib>Cheng, Ju</creatorcontrib><creatorcontrib>Zhang, Ryan Y</creatorcontrib><creatorcontrib>Meng, Meng</creatorcontrib><creatorcontrib>Smalley, Matthew</creatorcontrib><creatorcontrib>Chen, Pin-Jung</creatorcontrib><creatorcontrib>Tang, Xinghong</creatorcontrib><creatorcontrib>Tseng, Patrick</creatorcontrib><creatorcontrib>Bao, Lirong</creatorcontrib><creatorcontrib>Huang, Tzu-Yang</creatorcontrib><creatorcontrib>Zhou, Dongjing</creatorcontrib><creatorcontrib>Liu, Yupin</creatorcontrib><creatorcontrib>Chai, Xiaoshu</creatorcontrib><creatorcontrib>Zhang, Haibo</creatorcontrib><creatorcontrib>Zhou, Anqi</creatorcontrib><creatorcontrib>Agopian, Vatche G</creatorcontrib><creatorcontrib>Posadas, Edwin M</creatorcontrib><creatorcontrib>Shyue, Jing-Jong</creatorcontrib><creatorcontrib>Jonas, Steven J</creatorcontrib><creatorcontrib>Weiss, Paul S</creatorcontrib><creatorcontrib>Li, Mengyuan</creatorcontrib><creatorcontrib>Zheng, Guangjuan</creatorcontrib><creatorcontrib>Yu, Hsiao-Hua</creatorcontrib><creatorcontrib>Zhao, Meiping</creatorcontrib><creatorcontrib>Tseng, Hsian-Rong</creatorcontrib><creatorcontrib>Zhu, Yazhen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Science advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dong, Jiantong</au><au>Jan, Yu Jen</au><au>Cheng, Ju</au><au>Zhang, Ryan Y</au><au>Meng, Meng</au><au>Smalley, Matthew</au><au>Chen, Pin-Jung</au><au>Tang, Xinghong</au><au>Tseng, Patrick</au><au>Bao, Lirong</au><au>Huang, Tzu-Yang</au><au>Zhou, Dongjing</au><au>Liu, Yupin</au><au>Chai, Xiaoshu</au><au>Zhang, Haibo</au><au>Zhou, Anqi</au><au>Agopian, Vatche G</au><au>Posadas, Edwin M</au><au>Shyue, Jing-Jong</au><au>Jonas, Steven J</au><au>Weiss, Paul S</au><au>Li, Mengyuan</au><au>Zheng, Guangjuan</au><au>Yu, Hsiao-Hua</au><au>Zhao, Meiping</au><au>Tseng, Hsian-Rong</au><au>Zhu, Yazhen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells</atitle><jtitle>Science advances</jtitle><addtitle>Sci Adv</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>5</volume><issue>7</issue><spage>eaav9186</spage><pages>eaav9186-</pages><issn>2375-2548</issn><eissn>2375-2548</eissn><abstract>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.</abstract><cop>United States</cop><pub>American Association for the Advancement of Science</pub><pmid>31392269</pmid><doi>10.1126/sciadv.aav9186</doi><orcidid>https://orcid.org/0000-0001-5570-2470</orcidid><orcidid>https://orcid.org/0000-0002-8696-8738</orcidid><orcidid>https://orcid.org/0000-0002-2130-8085</orcidid><orcidid>https://orcid.org/0000-0003-0942-5905</orcidid><orcidid>https://orcid.org/0000-0002-3603-6932</orcidid><orcidid>https://orcid.org/0000-0001-8649-1346</orcidid><orcidid>https://orcid.org/0000-0002-6143-078X</orcidid><orcidid>https://orcid.org/0000-0001-7063-711X</orcidid><orcidid>https://orcid.org/0000-0002-4664-1845</orcidid><orcidid>https://orcid.org/0000-0002-3122-4053</orcidid><orcidid>https://orcid.org/0000-0002-6536-5647</orcidid><orcidid>https://orcid.org/0000-0002-2962-2933</orcidid><orcidid>https://orcid.org/0000-0002-9715-6292</orcidid><orcidid>https://orcid.org/0000-0001-5527-6248</orcidid><orcidid>https://orcid.org/0000-0002-8508-659X</orcidid><orcidid>https://orcid.org/0000-0001-9358-3054</orcidid><orcidid>https://orcid.org/0000-0002-8111-0249</orcidid><orcidid>https://orcid.org/0000-0002-2342-5058</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2375-2548
ispartof Science advances, 2019-07, Vol.5 (7), p.eaav9186
issn 2375-2548
2375-2548
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6669017
source MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Adult
Aged
Anaplastic Lymphoma Kinase - chemistry
Anaplastic Lymphoma Kinase - genetics
Cancer
Carcinoma, Non-Small-Cell Lung - blood
Carcinoma, Non-Small-Cell Lung - chemistry
Carcinoma, Non-Small-Cell Lung - genetics
Carcinoma, Non-Small-Cell Lung - pathology
Cell Line, Tumor
Chemistry
Click Chemistry - methods
Female
Gene Rearrangement - genetics
Health and Medicine
Humans
Male
Middle Aged
Nanostructures - chemistry
Neoplasm Staging
Neoplastic Cells, Circulating - chemistry
Protein-Tyrosine Kinases - chemistry
Protein-Tyrosine Kinases - genetics
Proto-Oncogene Proteins - chemistry
Proto-Oncogene Proteins - genetics
RNA, Messenger - blood
RNA, Messenger - isolation & purification
SciAdv r-articles
Silicon - chemistry
title Covalent chemistry on nanostructured substrates enables noninvasive quantification of gene rearrangements in circulating tumor cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T01%3A59%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Covalent%20chemistry%20on%20nanostructured%20substrates%20enables%20noninvasive%20quantification%20of%20gene%20rearrangements%20in%20circulating%20tumor%20cells&rft.jtitle=Science%20advances&rft.au=Dong,%20Jiantong&rft.date=2019-07-01&rft.volume=5&rft.issue=7&rft.spage=eaav9186&rft.pages=eaav9186-&rft.issn=2375-2548&rft.eissn=2375-2548&rft_id=info:doi/10.1126/sciadv.aav9186&rft_dat=%3Cproquest_pubme%3E2270010448%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2270010448&rft_id=info:pmid/31392269&rfr_iscdi=true