Peritumor Mucosa in Advanced Laryngeal Carcinoma Exhibits an Aberrant Proangiogenic Signature Distinctive from the Expression Pattern in Adjacent Tumor Tissue.

ETS-1 HIF HIF switch HIF-1α HIF-2α HIF-3α VEGF-A field cancerization laryngeal carcinoma miR-210

Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
05 Apr 2024
Historique:
received: 02 03 2024
revised: 31 03 2024
accepted: 03 04 2024
medline: 12 4 2024
pubmed: 12 4 2024
entrez: 12 4 2024
Statut: epublish

Résumé

The field cancerization theory is an important paradigm in head and neck carcinoma as its oncological repercussions affect treatment outcomes in diverse ways. The aim of this study is to assess the possible interconnection between peritumor mucosa and the process of tumor neoangiogenesis. Sixty patients with advanced laryngeal carcinoma were enrolled in this study. The majority of patients express a canonical HIF-upregulated proangiogenic signature with almost complete predominancy of HIF-1α overexpression and normal expression levels of the HIF-2α isoform. Remarkably, more than 60% of the whole cohort also exhibited an HIF-upregulated proangiogenic signature in the peritumoral benign mucosa. Additionally, the latter subgroup had a distinctly shifted phenotype towards HIF-2α upregulation compared to the one in tumor tissue, i.e., a tendency towards an HIF switch is observed in contrast to the dominated by HIF-1α tumor phenotype. ETS-1 displays stable and identical significant overexpression in both the proangiogenic phenotypes present in tumor and peritumoral mucosa. In the current study, we report for the first time the existence of an abnormal proangiogenic expression profile present in the peritumoral mucosa in advanced laryngeal carcinoma when compared to paired distant laryngeal mucosa. Moreover, we describe a specific phenotype of this proangiogenic signature that is significantly different from the one present in tumor tissue as we delineate both phenotypes, quantitively and qualitatively. This finding is cancer heterogeneity, per se, which extends beyond the "classical" borders of the malignancy, and it is proof of a strong interconnection between field cancerization and one of the classical hallmarks of cancer-the process of tumor neoangiogenesis.

Identifiants

pubmed: 38607072
pii: cells13070633
doi: 10.3390/cells13070633
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : European Commission
ID : Project: BG-RRP-2.004-0004-C01, group 3.1.5

Auteurs

Silva G Kyurkchiyan (SG)

Molecular Medicine Center, Medical University-Sofia, 1463 Sofia, Bulgaria.

Gergana Stancheva (G)

Molecular Medicine Center, Medical University-Sofia, 1463 Sofia, Bulgaria.

Veronika Petkova (V)

Molecular Medicine Center, Medical University-Sofia, 1463 Sofia, Bulgaria.

Stiliana Panova (S)

Molecular Medicine Center, Medical University-Sofia, 1463 Sofia, Bulgaria.

Venera Dobriyanova (V)

Department of ENT, Medical University-Sofia, 1463 Sofia, Bulgaria.

Iglika Stancheva (I)

Department of ENT, Medical University-Sofia, 1463 Sofia, Bulgaria.

Venelin Marinov (V)

Department of ENT, Medical University-Sofia, 1463 Sofia, Bulgaria.

Zahari Zahariev (Z)

Department of ENT, Medical University-Sofia, 1463 Sofia, Bulgaria.

Radka P Kaneva (RP)

Molecular Medicine Center, Medical University-Sofia, 1463 Sofia, Bulgaria.

Todor M Popov (TM)

Department of ENT, Medical University-Sofia, 1463 Sofia, Bulgaria.

Classifications MeSH