Evidence map›Paper›PMID 40504344›Full record

ArticleDiscover oncology2025

Differential expression of capecitabine-related metabolic enzymes in hepatocellular carcinoma and its clinical value: a retrospective cohort study.

Jianing Lu, Zhiqi Yin, Yan Zhuang, Zhenglu Wang, Hong Zheng, Lei Cao, Dejun Kong, Jinliang Duan, Shaofeng Chen, Tao Chen

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Jianing Lu *The First Central Clinical College, Tianjin Medical University, No. 24 Fukang Road, Nankai District, Tianjin, 300070, China.
Zhiqi Yin *Department of Pathology, Tianjin First Central Hospital, First Central Clinical College, Tianjin Medical University, No. 24 Fukang Road, Nankai District, Tianjin, 300192, China.
Yan ZhuangDepartment of Health Service, Military Health Education Section, Logistics College of People's Armed Police Force, No. 1 Hui Zhi Huan Road, Dong Li District, Tianjin, 300309, China.
Zhenglu WangThe Biospecimen Resource Sharing Center, Tianjin First Central Hospital, First Central Clinical College, Tianjin Medical University, No. 24 Fukang Road, Nankai District, Tianjin, 300192, China. 13920474643@163.com.
Hong ZhengOrgan Transplant Department, Tianjin First Central Hospital, First Central Clinical College, Tianjin Medical University, No. 24 Fukang Road, Nankai District, Tianjin, 300192, China. zhenghongyx@139.com.
Lei CaoThe Biospecimen Resource Sharing Center, Tianjin First Central Hospital, First Central Clinical College, Tianjin Medical University, No. 24 Fukang Road, Nankai District, Tianjin, 300192, China.
Dejun KongSchool of Medicine, Nankai University, No. 94, Weijin Road, Nankai District, Tianjin, 300071, China.
Jinliang DuanSchool of Medicine, Nankai University, No. 94, Weijin Road, Nankai District, Tianjin, 300071, China.
Shaofeng ChenSchool of Medicine, Nankai University, No. 94, Weijin Road, Nankai District, Tianjin, 300071, China.
Tao ChenSchool of Medicine, Nankai University, No. 94, Weijin Road, Nankai District, Tianjin, 300071, China.

Funding

the General Project of the Natural Science Foundation of Tianjin 22JCYBJC01230
6 · The paper itself

Abstract

backgroundCapecitabine (CAP) is widely used in cancer treatment for its oral convenience and tumor targeting. However, its effectiveness in hepatocellular carcinoma (HCC) is suboptimal, possibly due to metabolic enzyme expression differences. This study aims to analyze these enzymes' expression differences and explore their correlation with clinical pathological factors, to inform personalized CAP treatment.

methodsThis retrospective study used Immunohistochemistry (IHC) to analyze tumor and non-tumorous samples from HCC patients for CAP metabolic enzyme expression. PRM protein quantification was performed on 10% of samples to validate IHC results. Clinical and pathological data were collected, and multivariable linear regression was used to identify independent risk factors.

resultsThis study analyzed 60 HCC patients with hepatitis B and cirrhosis, revealing significant differences in CAP metabolic enzymes expression between tumor and non-tumorous tissues, with greater individual differences in tumors. Cytidine deaminase (CDA) levels in tumors decreased as liver function deteriorated (P = 0.023), while thymidine phosphorylase (TP) levels increased (P < 0.001). Tumor tissue had lower levels of carboxylesterase 1-2 (CES1-2), CDA, and dihydropyrimidine dehydrogenase (DPYD) but higher TP levels than non-tumorous and normal liver tissues. In tumor tissue, CDA (CV: 118.70%, SD: 3.897) and CES2 (CV: 94.90%, SD: 2.910) showed the greatest individual variability. Multivariable linear regression identified independent risk factors affecting CAP metabolic enzyme expression.

conclusionThis study has found significant variability in the expression of CAP metabolic enzymes across individuals and tissues. Developing a treatment flowchart based on metabolic enzymes provides a foundation for personalized HCC treatment and enhances the effectiveness of CAP therapy. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

CapecitabineClinical pathological correlationHepatocellular carcinomaIndividual variabilityMetabolic enzymes

Identifiers

PMID40504344
PMCPMC12162402

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