Microproteomic profiling of high-grade squamous intraepithelial lesion of the cervix: insight into biological mechanisms of dysplasia and new potential diagnostic markers

Purpose High-grade squamous intraepithelial lesion (HSIL) is a known precursor for squamous cell carcinoma of uterine cervix. Although it is known that SILs are associated to infection by human papillomavirus, downstream biological mechanisms are still poorly described. In this study, we compared th...

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Hauptverfasser: Pottier, Charles Albert (VerfasserIn) , Kriegsmann, Mark (VerfasserIn) , Fresnais, Margaux (VerfasserIn) , Longuespée, Rémi (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2019
In: Proteomics. Clinical applications
Year: 2018, Jahrgang: 13, Heft: 1
ISSN:1862-8354
DOI:10.1002/prca.201800052
Online-Zugang:Verlag, Volltext: https://doi.org/10.1002/prca.201800052
Verlag: https://onlinelibrary.wiley.com/doi/abs/10.1002/prca.201800052
Volltext
Verfasserangaben:Charles Pottier, Mark Kriegsmann, Deborah Alberts, Nicolas Smargiasso, Dominique Baiwir, Gabriel Mazzucchelli, Michael Herfs, Margaux Fresnais, Rita Casadonte, Philippe Delvenne, Edwin De Pauw, and Rémi Longuespée

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245 1 0 |a Microproteomic profiling of high-grade squamous intraepithelial lesion of the cervix  |b insight into biological mechanisms of dysplasia and new potential diagnostic markers  |c Charles Pottier, Mark Kriegsmann, Deborah Alberts, Nicolas Smargiasso, Dominique Baiwir, Gabriel Mazzucchelli, Michael Herfs, Margaux Fresnais, Rita Casadonte, Philippe Delvenne, Edwin De Pauw, and Rémi Longuespée 
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520 |a Purpose High-grade squamous intraepithelial lesion (HSIL) is a known precursor for squamous cell carcinoma of uterine cervix. Although it is known that SILs are associated to infection by human papillomavirus, downstream biological mechanisms are still poorly described. In this study, we compared the microproteomic profile of HSIL to normal tissues: ectocervix (ectoC) and endocervix (endoC). Experimental design Tissue regions of endoC, ectoC, and HSlL were collected by laser microdissection (3500 cells each) from five patients. Samples were processed and analyzed using our recently developed laser microdissection-based microproteomic method. Tissues were compared in order to retrieve HSIL's proteomic profile. Potentially interesting proteins for pathology were stained by immunohistochemistry. Results We identified 3072 proteins among the fifteen samples and 2386 were quantified in at least four out of the five biological replicates of at least one tissue type. We found 236 proteins more abundant in HSIL. Gene ontology enrichments revealed mechanisms of DNA replication and RNA splicing. Despite the squamous nature of HSIL, a common signature between HSIL and endoC could be found. Finally, potential new markers could support diagnosis of dysplasia in SILs. Conclusion and clinical relevance This microproteomic investigation of HSIL gives insights into the biology of cervical precancerous lesions. 
534 |c 2018 
650 4 |a cervical dysplasia 
650 4 |a laser microdissection 
650 4 |a microproteomics 
650 4 |a pathology 
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