Evidence map›Paper›PMID 40172728›Full record

ArticleDiscover oncology2025

Identification of CCDC58 as a potential predictive biomarker of immune cell infiltration in hepatocellular carcinoma.

Zishen Liu, Xiaotong Lin, Tingting Tan, Guozhu Xie, Ying 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. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Zishen Liu *Department of Radiation Oncology, Guangdong Province, Nanfang Hospital, Southern Medical University, Guangzhou Avenue North 1838, Guangzhou, 510515, China.
Xiaotong Lin *Department of Radiation Oncology, Guangdong Province, Nanfang Hospital, Southern Medical University, Guangzhou Avenue North 1838, Guangzhou, 510515, China.
Tingting TanDepartment of Radiation Oncology, Guangdong Province, Nanfang Hospital, Southern Medical University, Guangzhou Avenue North 1838, Guangzhou, 510515, China.
Guozhu XieDepartment of Radiation Oncology, Guangdong Province, Nanfang Hospital, Southern Medical University, Guangzhou Avenue North 1838, Guangzhou, 510515, China. xieguozhu@126.com.
Ying ChenDepartment of Pulmonary and Critical Care Medicine, The Sixth Hospital of Wuhan, Affiliated Hospital of Jianghan University, 168 Hongkong Road, Wuhan, 430000, Hubei, China. 18986197498@163.com.

Funding

Natural Science Foundation of Guangdong Province 2021A1515011537Natural Science Foundation of Hubei Province of China 2024AFC061Wuhan Medical Science Research Project WX23A83
6 · The paper itself

Abstract

backgroundMitochondrial dynamics play a critical role in the proper functioning of both the innate and adaptive immune systems. Coiled-coil domain-containing 58 (CCDC58), a mitochondrial-related gene, has been implicated in various diseases, including cancer and infections. However, its predictive value in immune cell infiltration in hepatocellular carcinoma (HCC) remains unexplored.

methodsIn this study, RNA-seq data from The Cancer Genome Atlas and multiple online datasets were analyzed to explore the correlation between CCDC58 and clinicopathological features, prognosis, related signaling pathways and immune cell infiltration in HCC. Furthermore, primary T cells were isolated and cell experiments such as cytotoxic assays and transwell assays were conducted to verify pivotal conclusions.

resultsWe found that CCDC58 expression levels were significantly increased in HCC tissues. High CCDC58 expression in HCC tissues was significantly correlated with the patients' TNM stage, histologic grade, AFP level, tumor status, and poor clinical outcomes. Furthermore, the high expression of CCDC58 conferred a decreased immune activated phenotype and poor immune cell infiltration, and was strongly associated with expression of immune cell exhaustion markers in HCC. After the knockdown of CCDC58 in HCC cell lines, we observed that cytotoxicity of primary T cells increased via decreasing PD-1 expression on T cells and migration ability of primary T cell enhanced.

conclusionOur study indicated that CCDC58 might serve as a potential predictive biomarker of immune cell infiltration in HCC and is correlated with poor prognosis in HCC patients.

Indexed as

BiomarkerCCDC58Hepatocellular carcinomaImmune cell infiltrationMitochondrial

Identifiers

PMID40172728
PMCPMC11965056

What Socratic holds

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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 Socratic graph.