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Integrative proteomic profiling of ovarian cancer cell lines reveals precursor cell associated proteins and functional status
被引:155
|作者:
Coscia, F.
[1
]
Watters, K. M.
[2
]
Curtis, M.
[2
]
Eckert, M. A.
[2
]
Chiang, C. Y.
[2
]
Tyanova, S.
[1
]
Montag, A.
[3
]
Lastra, R. R.
[3
]
Lengyel, E.
[2
]
Mann, M.
[1
]
机构:
[1] Max Planck Inst Biochem, Dept Prote & Signal Transduct, D-82152 Martinsried, Germany
[2] Univ Chicago, Gynecol Oncol Sect, Dept Obstet & Gynecol, Chicago, IL 60637 USA
[3] Univ Chicago Med, Dept Pathol, Chicago, IL 60637 USA
关键词:
FALLOPIAN-TUBE;
RETINOIC ACID;
MOLECULAR MARKER;
EXPRESSION;
IDENTIFICATION;
GROWTH;
QUANTIFICATION;
METASTASIS;
CRYSTALLIN;
CARCINOMA;
D O I:
10.1038/ncomms12645
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
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 410,000 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.
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页数:14
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