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Combining discovery and targeted proteomics reveals a prognostic signature in oral cancer.

Authors :
Carnielli CM
Macedo CCS
De Rossi T
Granato DC
Rivera C
Domingues RR
Pauletti BA
Yokoo S
Heberle H
Busso-Lopes AF
Cervigne NK
Sawazaki-Calone I
Meirelles GV
Marchi FA
Telles GP
Minghim R
Ribeiro ACP
Brandão TB
de Castro G Jr
González-Arriagada WA
Gomes A
Penteado F
Santos-Silva AR
Lopes MA
Rodrigues PC
Sundquist E
Salo T
da Silva SD
Alaoui-Jamali MA
Graner E
Fox JW
Coletta RD
Paes Leme AF
Source :
Nature communications [Nat Commun] 2018 Sep 05; Vol. 9 (1), pp. 3598. Date of Electronic Publication: 2018 Sep 05.
Publication Year :
2018

Abstract

Different regions of oral squamous cell carcinoma (OSCC) have particular histopathological and molecular characteristics limiting the standard tumor-node-metastasis prognosis classification. Therefore, defining biological signatures that allow assessing the prognostic outcomes for OSCC patients would be of great clinical significance. Using histopathology-guided discovery proteomics, we analyze neoplastic islands and stroma from the invasive tumor front (ITF) and inner tumor to identify differentially expressed proteins. Potential signature proteins are prioritized and further investigated by immunohistochemistry (IHC) and targeted proteomics. IHC indicates low expression of cystatin-B in neoplastic islands from the ITF as an independent marker for local recurrence. Targeted proteomics analysis of the prioritized proteins in saliva, combined with machine-learning methods, highlights a peptide-based signature as the most powerful predictor to distinguish patients with and without lymph node metastasis. In summary, we identify a robust signature, which may enhance prognostic decisions in OSCC and better guide treatment to reduce tumor recurrence or lymph node metastasis.

Details

Language :
English
ISSN :
2041-1723
Volume :
9
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
30185791
Full Text :
https://doi.org/10.1038/s41467-018-05696-2