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Serum exosomal proteomics analysis of lung adenocarcinoma to discover new tumor markers
BACKGROUND: Among the most aggressive and rapidly lethal types of lung cancer, lung adenocarcinoma is the most common type. Exosomes, as a hot area, play an influential role in cancer. By using proteomics analysis, we aimed to identify potential markers of lung adenocarcinoma in serum. METHODS: In o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925168/ https://www.ncbi.nlm.nih.gov/pubmed/35291954 http://dx.doi.org/10.1186/s12885-022-09366-x |
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author | Liu, Shanshan Tian, Wenjuan Ma, Yuefeng Li, Jiaji Yang, Jun Li, Burong |
author_facet | Liu, Shanshan Tian, Wenjuan Ma, Yuefeng Li, Jiaji Yang, Jun Li, Burong |
author_sort | Liu, Shanshan |
collection | PubMed |
description | BACKGROUND: Among the most aggressive and rapidly lethal types of lung cancer, lung adenocarcinoma is the most common type. Exosomes, as a hot area, play an influential role in cancer. By using proteomics analysis, we aimed to identify potential markers of lung adenocarcinoma in serum. METHODS: In our study, we used the ultracentrifugation method to isolate serum exosomes. The Liquid chromatography-mass spectrometry (LC–MS) and bioinformatics analysis were used to identify potential serum exosomal proteins with altered expression among patients with advanced lung adenocarcinoma, early lung adenocarcinoma, and healthy controls. A western blot (WB) was performed to confirm the above differential expression levels in a separate serum sample-isolated exosome, and immunohistochemistry (IHC) staining was conducted to detect expression levels of the above differential proteins of serum exosomes in lung adenocarcinoma tissues and adjacent tissues. Furthermore, we compared different expression models of the above differential proteins in serum and exosomes. RESULT: According to the ITGAM (Integrin alpha M chain) and CLU (Clusterin) were differentially expressed in serum exosomes among different groups as well as tumor tissues and adjacent tissues. ITGAM was significantly and specifically enriched in exosomes. As compared to serum, CLU did not appear to be significantly enriched in exosomes. ITGAM and CLU were identified as serum exosomal protein markers of lung adenocarcinoma. CONCLUSIONS: This study can provide novel ideas and a research basis for targeting lung adenocarcinoma treatment as a preliminary study. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09366-x. |
format | Online Article Text |
id | pubmed-8925168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89251682022-03-23 Serum exosomal proteomics analysis of lung adenocarcinoma to discover new tumor markers Liu, Shanshan Tian, Wenjuan Ma, Yuefeng Li, Jiaji Yang, Jun Li, Burong BMC Cancer Research BACKGROUND: Among the most aggressive and rapidly lethal types of lung cancer, lung adenocarcinoma is the most common type. Exosomes, as a hot area, play an influential role in cancer. By using proteomics analysis, we aimed to identify potential markers of lung adenocarcinoma in serum. METHODS: In our study, we used the ultracentrifugation method to isolate serum exosomes. The Liquid chromatography-mass spectrometry (LC–MS) and bioinformatics analysis were used to identify potential serum exosomal proteins with altered expression among patients with advanced lung adenocarcinoma, early lung adenocarcinoma, and healthy controls. A western blot (WB) was performed to confirm the above differential expression levels in a separate serum sample-isolated exosome, and immunohistochemistry (IHC) staining was conducted to detect expression levels of the above differential proteins of serum exosomes in lung adenocarcinoma tissues and adjacent tissues. Furthermore, we compared different expression models of the above differential proteins in serum and exosomes. RESULT: According to the ITGAM (Integrin alpha M chain) and CLU (Clusterin) were differentially expressed in serum exosomes among different groups as well as tumor tissues and adjacent tissues. ITGAM was significantly and specifically enriched in exosomes. As compared to serum, CLU did not appear to be significantly enriched in exosomes. ITGAM and CLU were identified as serum exosomal protein markers of lung adenocarcinoma. CONCLUSIONS: This study can provide novel ideas and a research basis for targeting lung adenocarcinoma treatment as a preliminary study. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09366-x. BioMed Central 2022-03-15 /pmc/articles/PMC8925168/ /pubmed/35291954 http://dx.doi.org/10.1186/s12885-022-09366-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Liu, Shanshan Tian, Wenjuan Ma, Yuefeng Li, Jiaji Yang, Jun Li, Burong Serum exosomal proteomics analysis of lung adenocarcinoma to discover new tumor markers |
title | Serum exosomal proteomics analysis of lung adenocarcinoma to discover new tumor markers |
title_full | Serum exosomal proteomics analysis of lung adenocarcinoma to discover new tumor markers |
title_fullStr | Serum exosomal proteomics analysis of lung adenocarcinoma to discover new tumor markers |
title_full_unstemmed | Serum exosomal proteomics analysis of lung adenocarcinoma to discover new tumor markers |
title_short | Serum exosomal proteomics analysis of lung adenocarcinoma to discover new tumor markers |
title_sort | serum exosomal proteomics analysis of lung adenocarcinoma to discover new tumor markers |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925168/ https://www.ncbi.nlm.nih.gov/pubmed/35291954 http://dx.doi.org/10.1186/s12885-022-09366-x |
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