Evidence map›Paper›PMID 41501937›Full record

ArticleEuropean journal of medical research2026

Therapeutic potential of CDK8 inhibitor combined with sorafenib for hepatocellular carcinoma: mechanistic insights and in vitro validation.

Li Gao, Hong Wu, Sheng-Yuan Du, Zi-Li Lv

Abstract read
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Article in European journal of medical research, 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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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

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Li GaoDepartment of Pathology, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Rd, Nanning, Guangxi Zhuang Autonomous Region, 530021, People's Republic of China.
Hong WuDepartment of Anesthesiology, Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology, No. 1095 Jiefang Avenue, Wuhan, Hubei, 430000, People's Republic of China.
Sheng-Yuan DuDepartment of Pathology, Qingdao Municipal Hospital, No. 5 Donghai Middle Rd, Qingdao, Shandong, 266000, People's Republic of China.
Zi-Li LvDepartment of Pathology, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Rd, Nanning, Guangxi Zhuang Autonomous Region, 530021, People's Republic of China. lvzili_gxmu@163.com.

Funding

Guangxi Medical and Health Appropriate Technology Development and Promotion Application Project S2022084
6 · The paper itself

Abstract

backgroundAlthough the prognosis of hepatocellular carcinoma (HCC) has been improved significantly due to diagnostic innovation and treatment optimization, HCC remains highly lethal, necessitating novel therapeutic targets. MATERIALS AND

methodsCDK8 expression was assessed in 75 HCC and paracancerous tissues by immunohistochemistry. Integrated analysis of 3969 HCC and 3245 non-tumor liver samples from RNA-seq and microarray datasets was performed. CDK8's functional mechanisms were explored through genetic alteration, immune infiltration, co-expression networks, and single-cell RNA-seq analyses. In vitro experiments including cell proliferation assay, scratch assay and transwell assay were conducted for investigating the effect of combined use of CDK8 inhibitor MSC2530818 and sorafenib on the biological functions of Huh7 cells.

resultsCDK8 was significantly overexpressed in HCC tissues, correlating with immune cell infiltration and advanced clinical stage. Single-cell analysis revealed prominent CDK8 expression in T/NK cells, myeloid cells, and cancer cells from advanced HCC samples. The carcinogenic role of CDK8 in HCC might be explained by the enrichment of co-expressed genes in biological processes including mRNA metabolic process, cell division and DNA conformation change. Combination of CDK8 inhibitor and sorafenib exerted more potent inhibition on cell growth, migration and invasion of Huh7 cells than monotherapy.

conclusionCDK8 is highly expressed in HCC tissues, suggesting its oncogenic role. Our in vitro findings demonstrate that the CDK8 inhibitor MSC2530818 synergizes with sorafenib to enhance anti-tumor efficacy against HCC cells, supporting further investigation of this combination strategy.

Indexed as

CDK8Hepatocellular carcinomaIHCIn-vitro experimentsSorafenib

Identifiers

PMID41501937
PMCPMC12870335

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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.