Label-Free Semiquantitative Liquid Chromatography-Tandem Mass Spectrometry Proteomics Analysis of Laryngeal/Hypopharyngeal Squamous Cell Carcinoma on Formalin-Fixed, Paraffin-Embedded Tissue Samples - a Pilot Study.
Aged
Biomarkers, Tumor
/ metabolism
Carcinoma, Squamous Cell
/ metabolism
Chromatography, Liquid
/ methods
Female
Follow-Up Studies
Formaldehyde
/ chemistry
Humans
Hypopharyngeal Neoplasms
/ metabolism
Laryngeal Neoplasms
/ metabolism
Male
Middle Aged
Paraffin Embedding
/ methods
Pilot Projects
Prognosis
Proteome
/ analysis
Tandem Mass Spectrometry
/ methods
Biomarker discovery
LC/MS
Laryngeal cancer
Proteomics
Squamous cell carcinoma
Journal
Pathology oncology research : POR
ISSN: 1532-2807
Titre abrégé: Pathol Oncol Res
Pays: Switzerland
ID NLM: 9706087
Informations de publication
Date de publication:
Oct 2020
Oct 2020
Historique:
received:
25
07
2019
accepted:
11
06
2020
pubmed:
22
6
2020
medline:
13
7
2021
entrez:
22
6
2020
Statut:
ppublish
Résumé
Squamous cell carcinoma (SCC) of the head and neck region is the sixth most frequent malignancy with high mortality rate. Due to its poor prognosis it is considered a growing public health problem worldwide inspite of existing treatment modalities. Thus, early diagnosis of new diseases and recurrences is emerging on one hand, but on the other hand troublesome in the lack of reliable tumor markers in this field. The rapid development of proteomics has opened new perspectives in tumor marker discovery. Liquid chromatography/mass spectrometry (LC/MS) as the gold standard in proteomics enables the semi-quantitative analysis of proteins within various tissues. Abundance differences between tumor and normal tissue also can be interpreted as tumor specific changes. The aim of this study was to identify potential tumor markers of laryngeal/hypopharyngeal SCC by revealing abundance changes between cancerous and the surrounding phenotypically healthy tissue. After separating the phenotypically cancerous and healthy parts of formalin-fixed paraffin-embedded tissues, each sample underwent protein recovery process and tryptic digestion for label-free semi-quantitative LC/MS analysis. Eight proteins showed significantly higher abundance in tumor including tenascin, transmembrane emp24 domain-containing protein 2, cytoplasmic dynein light chain 1, coactosin-like protein, small proline-rich protein 2D, nucleolin, U5 small nuclear RNP 200-kDa helicase and fatty aldehyde dehydrogenase. Desmoglein-1 and keratin type I cytoskeletal 9 were down-regulated in tumor. Using Ingenuity Pathway Analysis we mapped the signaling pathways these proteins play role in regarding other tumors. Based on these findings these proteins may serve as promising biomarkers in the fight against laryngeal/hypopharyngeal SCCs.
Identifiants
pubmed: 32564264
doi: 10.1007/s12253-020-00849-5
pii: 10.1007/s12253-020-00849-5
pmc: PMC7471140
doi:
Substances chimiques
Biomarkers, Tumor
0
Proteome
0
Formaldehyde
1HG84L3525
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2801-2807Subventions
Organisme : Nemzeti Kutatási Fejlesztési és Innovációs Hivatal
ID : GINOP-2.3.2-15
Organisme : Nemzeti Kutatási Fejlesztési és Innovációs Hivatal
ID : NKFIH PD-121187
Références
Expert Rev Proteomics. 2013 Aug;10(4):389-400
pubmed: 23992421
Pancreas. 2012 Mar;41(2):175-85
pubmed: 22015969
Mayo Clin Proc. 2008 Apr;83(4):489-501
pubmed: 18380996
Lancet. 2008 May 17;371(9625):1695-709
pubmed: 18486742
J Biol Chem. 2004 Feb 20;279(8):6235-43
pubmed: 14638685
Mol Cell Proteomics. 2019 Jan;18(1):151-161
pubmed: 30293968
Nat Commun. 2018 Sep 5;9(1):3598
pubmed: 30185791
Cancer Cell. 2012 Mar 20;21(3):309-22
pubmed: 22439926
Cancer Epidemiol Biomarkers Prev. 2009 Feb;18(2):541-50
pubmed: 19190158
PLoS One. 2014 Feb 27;9(2):e90181
pubmed: 24587265