Evidence map›Paper›PMID 42365150›Full record

ArticleAnnals of surgical oncology2026

SIGLEC12 Predicts Prognosis and Chemotherapeutic Vulnerability in Patients with Pancreatic Cancer.

Yanfei An, Yafen Chu, Jinbin Jia

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Article in Annals of surgical 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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5 · Who and what money

Authors and funding

3 authors.

Yanfei An *Department of Basic Medicine, Shanxi Medical University, Taiyuan, China. anyanfei1028@163.com.ORCID http://orcid.org/0009-0003-1054-2532
Yafen Chu *Academy of Medical Sciences and Labor Health Department, School of Public Health, Shanxi Medical University, Taiyuan, China.
Jinbin JiaDepartment of Basic Medicine, Shanxi Medical University, Taiyuan, China. jbjia@sxmu.edu.cn.

Funding

Fundamental Research Program of Shanxi Province 202403021222313Science and Technology Innovation Plan of Shanxi Higher Education Institutions 2023L205
6 · The paper itself

Abstract

backgroundEmerging evidence implicates sialic acid-binding immunoglobulin-like lectin (SIGLEC) family members as emerging immune checkpoints and as having a role in cancer progression. However, as a relatively unique SIGLEC member, SIGLEC12 has rarely been studied in cancer, and its clinical significance in pancreatic ductal adenocarcinoma (PDAC) remains largely unknown. This study aimed to investigate the expression pattern and prognostic value of SIGLEC12 in PDAC.

methodsA retrospective cohort of 145 patients with PDAC was enrolled. SIGLEC12 expression was assessed by immunohistochemistry on tumor microarrays. The association between SIGLEC12 and overall survival (OS) and recurrence-free survival (RFS) was evaluated using the Kaplan-Meier method and Cox regression analysis. The potential effect modification of SIGLEC12 was assessed by interaction analyses.

resultsSIGLEC12 expression was significantly upregulated in PDAC tissues at both protein and messenger RNA levels (P < 0.001). High SIGLEC12 expression was associated with poorer OS and RFS and was an independent prognostic factor (OS: hazard ratio [HR] 1.928, P = 0.0004; RFS: HR 1.569, P = 0.022). Interaction analyses revealed that the prognostic effects of carbohydrate antigen 19-9 (CA19‑9) and adjuvant chemotherapy (ACT) were significantly modified by SIGLEC12. Notably, elevated CA19-9 predicted poorer survival, and ACT improved survival only in patients with low SIGLEC12 expression and not in those with high SIGLEC12 expression.

conclusionsSIGLEC12 is frequently upregulated in PDAC and predicts poor prognosis. Notably, our exploratory findings suggest that SIGLEC12 may modify the prognostic effect of CA19‑9 and the therapeutic benefit of ACT. These findings position SIGLEC12 as a promising prognostic biomarker and novel therapeutic target in PDAC, with potential for further roles in refining risk stratification and guiding personalized treatment decisions.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCarcinoma, Pancreatic DuctalNeoplasm Recurrence, LocalPancreatic NeoplasmsAgedFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesRNA, MessengerSurvival RateBiomarkers, TumorRNA, MessengerAdjuvant chemotherapyCA19-9Pancreatic ductal adenocarcinomaPrognosisSIGLEC12

Identifiers

PMID42365150

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.