Evidence map›Paper›PMID 42730210›Full record

ArticleWorld journal of oncology2026

Siglec-15 Expression in Gastric Carcinoma and Its Association With Clinicopathological Variables.

Sara Al Badr, Abdelkader Battah, Ahmad Alsughayer, Fanar Alsmarat, Khalid Halahleh, Maher Sughayer

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Article in World journal of oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sara Al BadrDepartment of Pathology and Laboratory Medicine, King Hussein Cancer Center, Amman 11941, Jordan.
Abdelkader BattahSchool of Medicine, University of Jordan, Amman 11941, Jordan.
Ahmad AlsughayerDepartment of Surgery, King Hussein Cancer Center, Amman 11941, Jordan.
Fanar AlsmaratDepartment of Anatomy, Physiology and Biochemistry, Faculty of Medicine, The Hashemite University, Zarqa 13133, Jordan.
Khalid HalahlehDepartment of Medicine, King Hussein Cancer Center, Amman, Jordan.
Maher SughayerDepartment of Pathology and Laboratory Medicine, King Hussein Cancer Center, Amman 11941, Jordan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gastric cancer remains the fifth most common malignancy worldwide and is often diagnosed at advanced stages with limited treatment options. Although immunotherapy targeting the programmed cell death protein-1 (PD-1)/programmed death-ligand 1 (PD-L1) has improved outcomes in several cancers, many patients exhibit resistance, necessitating alternative therapeutic strategies. Sialic acid-binding immunoglobulin-like lectin-15 (Siglec-15), a recently recognized immune suppressor, is overexpressed in tumor cells and tumor-associated macrophages (TAMs), and is largely absent from normal tissues, making it a promising immunotherapy target. Methods: This tissue microarray (TMA) study retrospectively collected formalin-fixed paraffin-embedded (FFPE) tissue specimens from 2015 to 2019 for 77 gastric cancer patients from King Hussein Cancer Center. Siglec-15 expression patterns in tumor cells and TAMs were analyzed and compared with clinicopathological features and patient outcomes. Survival was assessed using Kaplan-Meier analysis. Results: Siglec-15 expression was detected in 50.7% of tumor samples and 36.4% of TAMs. Membranous expression was significantly associated with tumor differentiation, with higher expression observed in moderately differentiated tumors (P = 0.048), while cytoplasmic and TAM expression showed no significant associations with clinical variables. Although not statistically significant, positive Siglec-15 expression-both membranous and cytoplasmic-was associated with shorter median overall survival (cytoplasmic: 30.62 vs. 74.92 months, P = 0.1790; membranous: 39.44 vs. 66.07 months, P = 0.5761). Established prognostic indicators such as age, clinical stage, and pT stage were significantly associated with overall survival. Conclusion: Siglec-15 is frequently expressed in gastric cancer and may contribute to immune evasion within the tumor microenvironment. Although no significant association with prognosis was found, its high expression underscores its potential as a novel immunotherapeutic target. Further studies are warranted to validate these findings and explore Siglec-15 clinical utility.

Indexed as

Gastric carcinomaImmune checkpointSiglec-15

Identifiers

PMID42730210
PMCPMC13568786

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