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Integrative proteomic profiling of ovarian cancer cell lines reveals precursor cell associated proteins and functional status
A cell line representative of human high-grade serous ovarian cancer (HGSOC) should not only resemble its tumour of origin at the molecular level, but also demonstrate functional utility in pre-clinical investigations. Here, we report the integrated proteomic analysis of 26 ovarian cancer cell lines...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007461/ https://www.ncbi.nlm.nih.gov/pubmed/27561551 http://dx.doi.org/10.1038/ncomms12645 |
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author | Coscia, F. Watters, K. M. Curtis, M. Eckert, M. A. Chiang, C. Y. Tyanova, S. Montag, A. Lastra, R. R. Lengyel, E. Mann, M. |
author_facet | Coscia, F. Watters, K. M. Curtis, M. Eckert, M. A. Chiang, C. Y. Tyanova, S. Montag, A. Lastra, R. R. Lengyel, E. Mann, M. |
author_sort | Coscia, F. |
collection | PubMed |
description | A cell line representative of human high-grade serous ovarian cancer (HGSOC) should not only resemble its tumour of origin at the molecular level, but also demonstrate functional utility in pre-clinical investigations. Here, we report the integrated proteomic analysis of 26 ovarian cancer cell lines, HGSOC tumours, immortalized ovarian surface epithelial cells and fallopian tube epithelial cells via a single-run mass spectrometric workflow. The in-depth quantification of >10,000 proteins results in three distinct cell line categories: epithelial (group I), clear cell (group II) and mesenchymal (group III). We identify a 67-protein cell line signature, which separates our entire proteomic data set, as well as a confirmatory publicly available CPTAC/TCGA tumour proteome data set, into a predominantly epithelial and mesenchymal HGSOC tumour cluster. This proteomics-based epithelial/mesenchymal stratification of cell lines and human tumours indicates a possible origin of HGSOC either from the fallopian tube or from the ovarian surface epithelium. |
format | Online Article Text |
id | pubmed-5007461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50074612016-09-14 Integrative proteomic profiling of ovarian cancer cell lines reveals precursor cell associated proteins and functional status Coscia, F. Watters, K. M. Curtis, M. Eckert, M. A. Chiang, C. Y. Tyanova, S. Montag, A. Lastra, R. R. Lengyel, E. Mann, M. Nat Commun Article A cell line representative of human high-grade serous ovarian cancer (HGSOC) should not only resemble its tumour of origin at the molecular level, but also demonstrate functional utility in pre-clinical investigations. Here, we report the integrated proteomic analysis of 26 ovarian cancer cell lines, HGSOC tumours, immortalized ovarian surface epithelial cells and fallopian tube epithelial cells via a single-run mass spectrometric workflow. The in-depth quantification of >10,000 proteins results in three distinct cell line categories: epithelial (group I), clear cell (group II) and mesenchymal (group III). We identify a 67-protein cell line signature, which separates our entire proteomic data set, as well as a confirmatory publicly available CPTAC/TCGA tumour proteome data set, into a predominantly epithelial and mesenchymal HGSOC tumour cluster. This proteomics-based epithelial/mesenchymal stratification of cell lines and human tumours indicates a possible origin of HGSOC either from the fallopian tube or from the ovarian surface epithelium. Nature Publishing Group 2016-08-26 /pmc/articles/PMC5007461/ /pubmed/27561551 http://dx.doi.org/10.1038/ncomms12645 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Coscia, F. Watters, K. M. Curtis, M. Eckert, M. A. Chiang, C. Y. Tyanova, S. Montag, A. Lastra, R. R. Lengyel, E. Mann, M. Integrative proteomic profiling of ovarian cancer cell lines reveals precursor cell associated proteins and functional status |
title | Integrative proteomic profiling of ovarian cancer cell lines reveals precursor cell associated proteins and functional status |
title_full | Integrative proteomic profiling of ovarian cancer cell lines reveals precursor cell associated proteins and functional status |
title_fullStr | Integrative proteomic profiling of ovarian cancer cell lines reveals precursor cell associated proteins and functional status |
title_full_unstemmed | Integrative proteomic profiling of ovarian cancer cell lines reveals precursor cell associated proteins and functional status |
title_short | Integrative proteomic profiling of ovarian cancer cell lines reveals precursor cell associated proteins and functional status |
title_sort | integrative proteomic profiling of ovarian cancer cell lines reveals precursor cell associated proteins and functional status |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007461/ https://www.ncbi.nlm.nih.gov/pubmed/27561551 http://dx.doi.org/10.1038/ncomms12645 |
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