Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1782428142077476864 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4839576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zhourong nanonetscollectcancersecretomefrompericellularspace AT kuangyi nanonetscollectcancersecretomefrompericellularspace AT zhoujie nanonetscollectcancersecretomefrompericellularspace AT duxuewen nanonetscollectcancersecretomefrompericellularspace AT lijie nanonetscollectcancersecretomefrompericellularspace AT shijunfeng nanonetscollectcancersecretomefrompericellularspace AT haburcakrichard nanonetscollectcancersecretomefrompericellularspace AT xubing nanonetscollectcancersecretomefrompericellularspace |