Evidence map›Paper›PMID 40866361›Full record

ArticleSignal transduction and targeted therapy2025

Transforming acidic coiled-coil-containing protein 3-mediated lipid metabolism reprogramming impairs CD8

Ying Li, Zule Chen, Dongdong Wang, Wei Du, Ningqi Zhu, Xiaotian Shen, Xiang Mao, Yinghan Su, Lunxiu Qin, Diyu Chen and 1 more

Abstract read
In one paragraph

Article in Signal transduction and targeted therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
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  5. Article
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  7. [Research progress on poor response, resistance mechanisms, and influencing factors of immunotherapy for hepatocellular carcinoma].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2026
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Conserved Functions of LARP1 Proteins in Eukaryotes.Wiley interdisciplinary reviews. RNA
    Review
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

11 authors.

Ying LiDepartment of General Surgery, Huashan Hospital (Baoshan Branch), Fudan University, Shanghai, China.
Zule ChenDepartment of General Surgery, Huashan Hospital (Baoshan Branch), Fudan University, Shanghai, China.
Dongdong WangDepartment of Radiology, Huashan Hospital (Baoshan Branch), Fudan University, Shanghai, China.
Wei DuDepartment of Breast Surgery, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.
Ningqi ZhuDepartment of General Surgery, Huashan Hospital (Baoshan Branch), Fudan University, Shanghai, China.
Xiaotian ShenDepartment of General Surgery, Huashan Hospital (Baoshan Branch), Fudan University, Shanghai, China.
Xiang MaoDepartment of General Surgery, Huashan Hospital (Baoshan Branch), Fudan University, Shanghai, China.
Yinghan SuHepatobiliary Surgery Center, Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Lunxiu QinHepatobiliary Surgery Center, Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China. qinlx@fudan.edu.cn.
Diyu ChenDepartment of General Surgery, Huashan Hospital (Baoshan Branch), Fudan University, Shanghai, China. 21618112@zju.edu.cn.
Huliang JiaDepartment of General Surgery, Huashan Hospital (Baoshan Branch), Fudan University, Shanghai, China. jbl-1@163.com.

Funding

China Postdoctoral Science Foundation 2024M750533National Natural Science Foundation of China (National Science Foundation of China) 82202974National Natural Science Foundation of China (National Science Foundation of China) 82430089
6 · The paper itself

Abstract

Recent evidence has highlighted immune checkpoint inhibitors as among the most promising immunotherapies for various malignancies. However, a significant proportion of HCC patients exhibit poor responses. Lipid metabolic heterogeneity is considered a key driver of cancer progression. However, the role of lipid metabolic reprogramming in HCC immunotherapy resistance remains poorly understood. Herein, we aimed to illuminate the potential relationship between lipid metabolic reprogramming and ICI resistance and provide novel strategies to increase the HCC immunotherapy response. Patients who received PD-1/PD-L1 inhibitors were enrolled. The effect of TACC3 on the tumor microenvironment was validated via single-cell RNA sequencing in HCC-bearing mouse models. Targeted metabolomics was performed to analyze the regulatory role of TACC3 in HCC metabolism. To address HCC immunotherapy resistance, we developed a targeted nucleic acid therapeutic utilizing N-acetylgalactosamine (GalNAc) to conjugate siTACC3. Through clinical cohort analysis, we found that TACC3 was overexpressed in HCC patients with poor response to immunotherapy. Furthermore, we demonstrated that silencing tumor-derived TACC3 optimizes the cytotoxicity of infiltrating CD8

Indexed as

Carcinoma, HepatocellularCD8-Positive T-LymphocytesLipid MetabolismLiver NeoplasmsAnimalsCell Line, TumorFemaleHumansMaleMetabolic ReprogrammingMiceTumor Microenvironment

Identifiers

PMID40866361
PMCPMC12391444

What OpenQuestion holds

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Registered trials

None linked

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.