Evidence map›Paper›PMID 39875668›Full record

ArticleJournal of gastrointestinal cancer2025

Bile-Derived cfDNA of Syncytin-1 and SLC7A11 as a Potential Molecular Marker for Early Diagnosis of Cholangiocarcinoma.

Jing He, Jingrong Qian, Xin Li, Xiaoyue Zhao, Weiwei Meng, Xuewei Zhuang

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Article in Journal of gastrointestinal cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 citing papers in PubMed.

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5 · Who and what money

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6 authors.

Jing He *Second Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Jingrong Qian *Department of Clinical Laboratory, Shandong Provincial Third Hospital, Shandong University, Jinan, Shandong, China.
Xin LiSecond Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Xiaoyue ZhaoSecond Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Weiwei MengDepartment of Clinical Laboratory, Shandong Provincial Third Hospital, Shandong University, Jinan, Shandong, China.
Xuewei ZhuangDepartment of Clinical Laboratory, Shandong Provincial Third Hospital, Shandong University, Jinan, Shandong, China. xue_2022@yeah.net.

Funding

Shandong Province Medical and Health Technology Project 202311001247Shandong Provincial Natural Science Foundation ZR2020MH321Shandong Provincial Third Hospital Research and Cultivation Fund Q2023003
6 · The paper itself

Abstract

purposeLiquid biopsy technology has received widespread attention in the early diagnosis of cholangiocarcinoma (CCA).

methodsWe collected bile samples from 48 patients with CCA and 48 patients with gallstones at Shandong Provincial third Hospital. We quantified bile circulating free DNA (cfDNA) of syncytin-1 and SLC7A11, calculated the correlation between syncytin-1 and SLC7A11 expression and clinical parameters by Spearman rank correlation, plotted Receiver Operating Characteristic (ROC) curves, and compared the Area Under Curve (AUC) values to explored early diagnostic utility in patients.

resultsWe first found the bile cfDNA of syncytin-1 and SLC7A11 levels in CCA were higher than in gallstones (3.06 vs. 1.32, p < 0.001; 2.39 vs. 1.30, p < 0.001). And there was significant correlation between syncytin-1 and SLC7A11 expression (p = 0.025). Additionally, bile cfDNA of syncytin-1 or SLC7A11 was differentially expressed in gallstones, cholangiocarcinoma stage I-II, and cholangiocarcinoma stage III-IV (p < 0.001; p < 0.001). The AUC of bile cfDNA of syncytin-1 was 0.805 (p < 0.001, specificity of 87.0%), the AUC of bile cfDNA of SLC7A11 was 0.755 (p < 0.001, specificity of 80.4%), and combination of bile cDNA of syncytin-1/SLC7A11/CA19-9 markers improved diagnostic efficiency in CCA patients (AUC: 0.927, p < 0.001).

conclusionThe bile cfDNA of syncytin-1 and SLC7A11 was high expression in cholangiocarcinoma, which may be used as a novel biomarker for early diagnosis.

Indexed as

BileBile Duct NeoplasmsBiomarkers, TumorCell-Free Nucleic AcidsCholangiocarcinomaAdultAgedEarly Detection of CancerFemaleHumansLiquid BiopsyMaleMiddle AgedROC CurveBiomarkers, TumorCell-Free Nucleic AcidsBile circulating free DNACholangiocarcinomaEarly diagnosisSLC7A11Syncytin-1

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