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A Hidden Human Proteome Signature Characterizes the Epithelial Mesenchymal Transition Program

Authors :
Michele Maffia
Marco Trerotola
Marina Damato
Isabelle Fournier
Julien Franck
Daniele Vergara
Tiziano Verri
Pasquale Simeone
Michel Salzet
University of Salento [Lecce]
Università degli studi 'G. d'Annunzio' Chieti-Pescara [Chieti-Pescara] (Ud'A)
Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U 1192 (PRISM)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)
Université de Lille-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)
SALZET, Michel
Vergara, D.
Verri, T.
Damato, M.
Trerotola, M.
Simeone, P.
Franck, J.
Fournier, I.
Salzet, M.
Maffia, M.
Source :
Current Pharmaceutical Design, Current Pharmaceutical Design, 2020, 26 (3), pp.372-375. ⟨10.2174/1381612826666200129091610⟩, Current Pharmaceutical Design, Bentham Science Publishers, 2020, 26 (3), pp.372-375. ⟨10.2174/1381612826666200129091610⟩
Publication Year :
2020
Publisher :
Bentham Science Publishers Ltd., 2020.

Abstract

Background: Molecular changes associated with the initiation of the epithelial to mesenchymal transition (EMT) program involve alterations of large proteome-based networks. The role of protein products mapping to non-coding genomic regions is still unexplored. Objective: The goal of this study was the identification of an alternative protein signature in breast cancer cellular models with a distinct expression of EMT markers. Methods: We profiled MCF-7 and MDA-MB-231 cells using liquid-chromatography mass/spectrometry (LCMS/ MS) and interrogated the OpenProt database to identify novel predicted isoforms and novel predicted proteins from alternative open reading frames (AltProts). Results: Our analysis revealed an AltProt and isoform protein signature capable of classifying the two breast cancer cell lines. Among the most highly expressed alternative proteins, we observed proteins potentially associated with inflammation, metabolism and EMT. Conclusion: Here, we present an AltProts signature associated with EMT. Further studies will be needed to define their role in cancer progression.

Details

ISSN :
13816128
Volume :
26
Database :
OpenAIRE
Journal :
Current Pharmaceutical Design
Accession number :
edsair.doi.dedup.....ebe996582126f9ed3e4f541e2520dc71
Full Text :
https://doi.org/10.2174/1381612826666200129091610