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.


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
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

2801-2807

Subventions

Organisme : Nemzeti Kutatási Fejlesztési és Innovációs Hivatal
ID : GINOP-2.3.2-15
Organisme : Nemzeti Kutatási Fejlesztési és Innovációs Hivatal
ID : NKFIH PD-121187

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Auteurs

Andras Burian (A)

Clinical Centre, Department of Otorhinolaryngology and Head and Neck Surgery, University of Pecs, Munkacsy M Str 2, Pecs, H-7621, Hungary.

Laszlo Lujber (L)

Clinical Centre, Department of Otorhinolaryngology and Head and Neck Surgery, University of Pecs, Munkacsy M Str 2, Pecs, H-7621, Hungary.

Imre Gerlinger (I)

Clinical Centre, Department of Otorhinolaryngology and Head and Neck Surgery, University of Pecs, Munkacsy M Str 2, Pecs, H-7621, Hungary.

Tamas Jarai (T)

Tolna County Balassa Janos Hospital, Beri Balogh Adam Str 5-7, Szekszard, H-7100, Hungary.

Eva Orosz (E)

Clinical Centre, Department of Otorhinolaryngology and Head and Neck Surgery, University of Pecs, Munkacsy M Str 2, Pecs, H-7621, Hungary.

Lilla Turiak (L)

MS Proteomics Research Group, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Magyar tudosok Blvd 2, Budapest, H-1117, Hungary.

Andras Acs (A)

MS Proteomics Research Group, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Magyar tudosok Blvd 2, Budapest, H-1117, Hungary.
Ph.D. School of Pharmaceutical Sciences, Semmelweis University, Ulloi Str 26, Budapest, H-1085, Hungary.

Zoltan Hegedus (Z)

Biological Research Centre of the Hungarian Academy of Sciences, Institute of Biophysics, Temesvari Blvd 62, Szeged, H-6726, Hungary.
Medical School, Institute of Biochemistry and Medical Chemistry, University of Pecs, Szigeti Str 12, Pecs, H-7624, Hungary.

Aniko Konigne Peter (AK)

Medical School, Institute of Bioanalysis, University of Pecs, Honved Str 1, Pecs, H-7624, Hungary.

Tamas Tornoczki (T)

Medical School, Institute of Pathology, University of Pecs, Szigeti Str 12, Pecs, H-7624, Hungary.

Katalin Gombos (K)

Clinical Centre, Department of Laboratory Medicine, University of Pecs, Ifjusag Str 13, Pecs, H-7624, Hungary.

Laszlo Mark (L)

Medical School, Institute of Biochemistry and Medical Chemistry, University of Pecs, Szigeti Str 12, Pecs, H-7624, Hungary. laszlo.mark@aok.pte.hu.
MTA-PTE Human Reproduction Research Group, Edesanyak str. 1, Pecs, H-7624, Hungary. laszlo.mark@aok.pte.hu.

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Classifications MeSH