Evidence map›Paper›PMID 39474998›Full record

ArticleEnvironmental toxicology2025

SERPING1 Reduces Cell Migration via ERK-MMP2-MMP-9 Cascade in Sorafenib- Resistant Hepatocellular Carcinoma.

Ching-Chuan Hsieh, Yuh-Harn Wu, Yi-Li Chen, Chun-I Wang, Chao-Jen Li, I-Hsiu Liu, Chen-Wei Chou, Yang-Hsiang Lin, Po-Shuan Huang, Te-Chia Huang and 1 more

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Article in Environmental toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Ching-Chuan HsiehDivision of General Surgery, Chang Gung Memorial Hospital, Chiayi, Taiwan.
Yuh-Harn WuDepartment of Cell Biology and Anatomy, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Yi-Li ChenDepartment of Cell Biology and Anatomy, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Chun-I WangDepartment of Biochemistry, School of Medicine, China Medical University, Taichung, Taiwan.
Chao-Jen LiDepartment of General & Gastroenterological Surgery, An Nan Hospital, China Medical University, Tainan, Taiwan.
I-Hsiu LiuDepartment of Cell Biology and Anatomy, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Chen-Wei ChouDepartment of Cell Biology and Anatomy, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Yang-Hsiang LinLiver Research Center, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Po-Shuan HuangDepartment of Biochemistry, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Te-Chia HuangDepartment of General & Gastroenterological Surgery, An Nan Hospital, China Medical University, Tainan, Taiwan.
Cheng-Yi ChenDepartment of Cell Biology and Anatomy, College of Medicine, National Cheng Kung University, Tainan, Taiwan.ORCID https://orcid.org/0000-0001-9397-4792

Funding

An Nan Hospital, China Medical University ANHRF112-40Chang Gung Memorial Hospital CORPG6M0101Ministry of Science and Technology of the People's Republic of China MOST 111-2320-B-006-023National Cheng Kung University Hospital NCKUH-11202064
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common primary hepatic malignant tumor, and it ranks 2nd in terms of mortality rate among all malignancies in Taiwan. Sorafenib is a multiple tyrosine kinase inhibitor that suppresses tumor cell proliferation and angiogenesis around tumors via different pathways. However, the survival outcome of advanced HCC patients treated with sorafenib is still unsatisfactory. Unfortunately, there are no clinically applicable biomarkers to predict sorafenib therapeutic efficiency in HCC thus far. We found that serpin peptidase inhibitor, clade G, member 1 (SERPING1) is highly associated with overall and recurrence-free survival rates in HCC patients and is also highly correlated with several clinical parameters. SERPING1 expression was increased with sorafenib in both the HCC cell extract and conditioned medium, which was also observed in sorafenib-resistant HepG2 and Huh7 cells. Sorafenib decreased cell viability and migration, which was similar to the effect of SERPING1 in HCC progression. Moreover, sorafenib inhibited both MMP-2 and MMP-9 activity and enhanced the expression of p-ERK in HCC cells. In summary, sorafenib reduces HCC cancer progression might through the p-ERK-MMP-2-MMP-9 cascade via upregulation of SERPING1. In the present study, the roles and molecular mechanisms of SERPING1 and its value as a marker for predicting sorafenib resistance and progression in HCC patients were examined. The results of the present study provide a deep understanding of the roles of SERPING1 in HCC sorafenib resistance, which can be applied to develop early diagnosis and prognosis evaluation methods and establish novel therapeutic targets for specifically treating HCC.

Indexed as

Antineoplastic AgentsCarcinoma, HepatocellularComplement C1 Inhibitor ProteinLiver NeoplasmsSorafenibCell Line, TumorCell MovementDrug Resistance, NeoplasmExtracellular Signal-Regulated MAP KinasesFemaleHumansMaleMatrix Metalloproteinase 2Matrix Metalloproteinase 9Antineoplastic AgentsComplement C1 Inhibitor ProteinExtracellular Signal-Regulated MAP KinasesMatrix Metalloproteinase 2Matrix Metalloproteinase 9SERPING1 protein, humanSorafenibcancer progressiondrug resistancehepatocellular carcinomaSERPING1sorafenib

Identifiers

PMID39474998
PMCPMC11726270

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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.