Galectin-8 Immunohistochemical Profile in Pancreatic Ductal Adenocarcinoma: Emerging Evidence for Its Prognostic Role.

galectin-8 histological pattern immunohistochemistry pancreatic ductal adenocarcinoma prognosis

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
15 Oct 2023
Historique:
received: 03 09 2023
revised: 29 09 2023
accepted: 05 10 2023
medline: 28 10 2023
pubmed: 28 10 2023
entrez: 28 10 2023
Statut: epublish

Résumé

Pancreatic ductal adenocarcinoma (PDAC) represents the most frequent pancreatic malignancy, with stromal and epithelial heterogeneity reflected in outcome variability. Therefore, a molecular classification is promoted based on the validation of new diagnostic and prognostic markers. Galectin-8 (Gal8) has been pointed out as a prognostic factor for survival in several types of tumors. Due to limited existing data on PDAC, our study aimed to evaluate the Gal8 profile in PDAC alongside its prognostic status. A total of 87 cases of PDAC were immunohistochemically investigated, and Gal8 immunoexpression was qualitatively and semi-quantitatively assessed and correlated with classical clinicopathological parameters and survival. Gal8 immunoexpression was identified to be mostly nuclear and cytoplasmic, followed by exclusively cytoplasmic and exclusively nuclear. A statistical analysis between Gal8 profiles defined by negative, low, or high scores and clinicopathological characteristics showed significant differences in tumor size, pN stage, and lympho-vascular invasion. Although a Cox regression analysis did not support the prognostic status of Gal8, and we did not confirm its relationship with OS, our results show that exclusively nuclear labeling was associated with an increased mean OS compared with cytoplasmic and nuclear labeling (29.37 vs. 17.93 months). To the best of our knowledge, this is the first study to report a detailed pattern of Gal8 immunostaining in PDAC and to correlate this pattern with clinicopathological characteristics and survival. Our results show that Gal8 immunoexpression is associated with a more aggressive phenotype, thus opening perspectives for larger studies to validate Gal8 as a prognostic factor.

Identifiants

pubmed: 37892036
pii: diagnostics13203215
doi: 10.3390/diagnostics13203215
pmc: PMC10606265
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Andreea Rusu (A)

Department of Morpho-Functional Sciences I-Histology, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iași, Romania.

Irina-Draga Caruntu (ID)

Department of Morpho-Functional Sciences I-Histology, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iași, Romania.
Department of Pathology, "Dr. C.I. Parhon" Clinical Hospital, 700503 Iasi, Romania.

Ludmila Lozneanu (L)

Department of Morpho-Functional Sciences I-Histology, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iași, Romania.
Department of Pathology, "Sf. Spiridon" Clinical Emergency County Hospital, 700111 Iasi, Romania.

Delia Gabriela Ciobanu (DG)

Department of Pathology, "Sf. Spiridon" Clinical Emergency County Hospital, 700111 Iasi, Romania.
Department of Morpho-Functional Sciences I-Morphopathology, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iași, Romania.

Cornelia Amalinei (C)

Department of Morpho-Functional Sciences I-Histology, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iași, Romania.

Simona-Eliza Giusca (SE)

Department of Pathology, "Dr. C.I. Parhon" Clinical Hospital, 700503 Iasi, Romania.
Department of Morpho-Functional Sciences I-Morphopathology, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iași, Romania.

Classifications MeSH