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Nanonets Collect Cancer Secretome from Pericellular Space

Identifying novel cancer biomarkers is important for early cancer detection as it can reduce mortality rates. The cancer secretome, the collection of all macromolecules secreted by a tumor cell, alters its composition compared to normal tissue, and this change plays an important role in the observat...

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Detalles Bibliográficos
Autores principales: Zhou, Rong, Kuang, Yi, Zhou, Jie, Du, Xuewen, Li, Jie, Shi, Junfeng, Haburcak, Richard, Xu, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839576/
https://www.ncbi.nlm.nih.gov/pubmed/27100780
http://dx.doi.org/10.1371/journal.pone.0154126
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author Zhou, Rong
Kuang, Yi
Zhou, Jie
Du, Xuewen
Li, Jie
Shi, Junfeng
Haburcak, Richard
Xu, Bing
author_facet Zhou, Rong
Kuang, Yi
Zhou, Jie
Du, Xuewen
Li, Jie
Shi, Junfeng
Haburcak, Richard
Xu, Bing
author_sort Zhou, Rong
collection PubMed
description Identifying novel cancer biomarkers is important for early cancer detection as it can reduce mortality rates. The cancer secretome, the collection of all macromolecules secreted by a tumor cell, alters its composition compared to normal tissue, and this change plays an important role in the observation of cancer progression. The collection and accurate analysis of cancer secretomes could lead to the discovery of novel biomarkers, thus improving outcomes of cancer treatment. We unexpectedly discovered that enzyme-instructed self-assembly (EISA) of a D-peptide hydrogelator results in nanonets/hydrogel around cancer cells that overexpress ectophosphatases. Here we show that these nanonets are able to rapidly collect proteins in the pericellular space (i.e., near the surface) of cancer cells. Because the secretory substances are at their highest concentration near the cell surface, the use of pericellular nanonets to collect the cancer secretome maximizes the yield and quality of samples, reduces pre-analytical variations, and allows the dynamic profiling of secretome samples. Thus, this new approach has great potential in identifying the heterotypic signaling in tumor microenvironments thereby improving the understanding of tumor microenvironments and accelerating the discovery of potential biomarkers in cancer biology. Data are available via ProteomeXchange with identifier PXD003924.
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spelling pubmed-48395762016-04-29 Nanonets Collect Cancer Secretome from Pericellular Space Zhou, Rong Kuang, Yi Zhou, Jie Du, Xuewen Li, Jie Shi, Junfeng Haburcak, Richard Xu, Bing PLoS One Research Article Identifying novel cancer biomarkers is important for early cancer detection as it can reduce mortality rates. The cancer secretome, the collection of all macromolecules secreted by a tumor cell, alters its composition compared to normal tissue, and this change plays an important role in the observation of cancer progression. The collection and accurate analysis of cancer secretomes could lead to the discovery of novel biomarkers, thus improving outcomes of cancer treatment. We unexpectedly discovered that enzyme-instructed self-assembly (EISA) of a D-peptide hydrogelator results in nanonets/hydrogel around cancer cells that overexpress ectophosphatases. Here we show that these nanonets are able to rapidly collect proteins in the pericellular space (i.e., near the surface) of cancer cells. Because the secretory substances are at their highest concentration near the cell surface, the use of pericellular nanonets to collect the cancer secretome maximizes the yield and quality of samples, reduces pre-analytical variations, and allows the dynamic profiling of secretome samples. Thus, this new approach has great potential in identifying the heterotypic signaling in tumor microenvironments thereby improving the understanding of tumor microenvironments and accelerating the discovery of potential biomarkers in cancer biology. Data are available via ProteomeXchange with identifier PXD003924. Public Library of Science 2016-04-21 /pmc/articles/PMC4839576/ /pubmed/27100780 http://dx.doi.org/10.1371/journal.pone.0154126 Text en © 2016 Zhou et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zhou, Rong
Kuang, Yi
Zhou, Jie
Du, Xuewen
Li, Jie
Shi, Junfeng
Haburcak, Richard
Xu, Bing
Nanonets Collect Cancer Secretome from Pericellular Space
title Nanonets Collect Cancer Secretome from Pericellular Space
title_full Nanonets Collect Cancer Secretome from Pericellular Space
title_fullStr Nanonets Collect Cancer Secretome from Pericellular Space
title_full_unstemmed Nanonets Collect Cancer Secretome from Pericellular Space
title_short Nanonets Collect Cancer Secretome from Pericellular Space
title_sort nanonets collect cancer secretome from pericellular space
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839576/
https://www.ncbi.nlm.nih.gov/pubmed/27100780
http://dx.doi.org/10.1371/journal.pone.0154126
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