Evidence map›Paper›PMID 40977659›Full record

ArticleWorld journal of gastrointestinal oncology2025

Irreversible electroporation combined with checkpoint blockade stimulates antitumor immune response in a hepatocellular carcinoma mouse model.

Yan-Li Xing, Hong-Mei Li, Xiao-Ming Pang, Ying Zhang, Ting Yang, Yan-Hong Li, De-Chuan Liu, Yang-Yang Ma, Li-Zhi Niu

Abstract read
In one paragraph

Article in World journal of gastrointestinal oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Yan-Li XingDepartment of Oncology, Guangzhou Fuda Cancer Hospital, Jinan University, Guangzhou 510655, Guangdong Province, China.
Hong-Mei LiDepartment of Oncology, Guangzhou Fuda Cancer Hospital, Jinan University, Guangzhou 510655, Guangdong Province, China.
Xiao-Ming PangDepartment of Oncology, Guangzhou Fuda Cancer Hospital, Jinan University, Guangzhou 510655, Guangdong Province, China.
Ying ZhangDepartment of Oncology, Guangzhou Fuda Cancer Hospital, Jinan University, Guangzhou 510655, Guangdong Province, China.
Ting YangDepartment of Oncology, Guangzhou Fuda Cancer Hospital, Jinan University, Guangzhou 510655, Guangdong Province, China.
Yan-Hong LiDepartment of Nursing, Guangzhou Fuda Cancer Hospital, Jinan University, Guangzhou 510665, Guangdong Province, China.
De-Chuan LiuDepartment of Oncology, Guangzhou Fuda Cancer Hospital, Jinan University, Guangzhou 510655, Guangdong Province, China.
Yang-Yang MaCentral Laboratory, Guangzhou Fuda Cancer Hospital, Jinan University, Guangzhou 510665, Guangdong Province, China.
Li-Zhi NiuDepartment of Oncology, Guangzhou Fuda Cancer Hospital, Jinan University, Guangzhou 510655, Guangdong Province, China. niuboshi@fudahospital.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIrreversible electroporation (IRE) represents an innovative localized technique for tumor ablation, possessing the capacity to activate the immune response of the host. However, this method alone is inadequate to halt cancer progression, necessitating the integration of additional strategies to achieve effective immunotherapy.

aimTo investigate the effects and underlying mechanisms of antitumor immunity derived from the synergistic application of IRE and anti-programmed cell death protein 1 (PD-1) therapy within a murine model of hepatocellular carcinoma.

methodsC57BL-6 mice with tumor growth were divided into four separate cohorts: Control group; IRE group; Anti-PD-1 group; And IRE + anti-PD-1 group. The infiltration levels of T, B, and natural killer cells within the tumors, as well as the plasma concentrations of T helper type 1 cytokines (interleukin-2, interferon-γ, and tumor necrosis factor-β), were evaluated. Real-time polymerase chain reaction was utilized to quantify the expression of cluster of differentiation (CD) 8 (a marker indicative of CD8

resultsThe results indicated that the IRE + anti-PD-1 group exhibited significantly heightened percentages of T lymphocyte infiltration, particularly CD4

conclusionThe combined application of IRE and checkpoint blockade elicits an antitumor immune response, leading to a more substantial reduction in tumor volume and improved therapeutic outcomes, thereby establishing a novel avenue for the ablation and immunotherapy of hepatocellular carcinoma.

Indexed as

Anticancer immunityCluster of differentiation 8+ T cellHepatocellular carcinomaIrreversible electroporationProgrammed cell death protein 1 blockade

Identifiers

PMID40977659
PMCPMC12444300

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