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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Veröffentlicht in: | Science advances 2019-07, Vol.5 (7), p.eaav9186 |
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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 |
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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 & 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 & 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 & 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> |
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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 |