Evidence map›Paper›PMID 39581706›Full record

ArticleJournal for immunotherapy of cancer2024

Integrated single-cell transcriptome and TCR profiles of hepatocellular carcinoma highlight the convergence on interferon signaling during immunotherapy.

Tianhao Li, Shengnan Guo, Chang Xu, Mingjie Zhang, Cheng Lyu, Huanhuan Xu, Zepeng Hou, Mingshuo Zhang, Xiaobo Li, Jing Ren and 4 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

14 authors.

Tianhao Li *Department of Phase 1 Trials Center, Harbin Medical University Cancer Hospital, Harbin, People's Republic of China.ORCID 0009-0000-9634-4016
Shengnan Guo *School of Basic Medical Sciences, Harbin Medical University, Harbin, People's Republic of China.ORCID 0000-0002-0867-9551
Chang Xu *Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, People's Republic of China.ORCID 0009-0002-7798-6907
Mingjie ZhangSchool of Basic Medical Sciences, Harbin Medical University, Harbin, People's Republic of China.
Cheng LyuSchool of Basic Medical Sciences, Harbin Medical University, Harbin, People's Republic of China.
Huanhuan XuSchool of Basic Medical Sciences, Harbin Medical University, Harbin, People's Republic of China.
Zepeng HouSchool of Basic Medical Sciences, Harbin Medical University, Harbin, People's Republic of China.
Mingshuo ZhangSchool of Basic Medical Sciences, Harbin Medical University, Harbin, People's Republic of China.
Xiaobo LiSchool of Basic Medical Sciences, Harbin Medical University, Harbin, People's Republic of China.
Jing RenDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, People's Republic of China.
Changqing LiuDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, People's Republic of China.
Dan KongDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Harbin, People's Republic of China dapenghao@hrbmu.edu.cn guangyuwang@hrbmu.edu.cn 600971@hrbmu.edu.cn.
Dapeng HaoDepartment of Phase 1 Trials Center, Harbin Medical University Cancer Hospital, Harbin, People's Republic of China dapenghao@hrbmu.edu.cn guangyuwang@hrbmu.edu.cn 600971@hrbmu.edu.cn.ORCID 0000-0002-9043-371X
Guangyu WangDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, People's Republic of China dapenghao@hrbmu.edu.cn guangyuwang@hrbmu.edu.cn 600971@hrbmu.edu.cn.ORCID 0000-0002-8171-515X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite the success of immune checkpoint inhibitor (ICI)-based combination therapies in hepatocellular carcinoma (HCC), its effectiveness remains confined to a subset of patients. The development of reliable, predictive markers is important for accurate patient stratification and further mechanistic understanding of therapy response.

methodsWe comprehensively analyzed paired single-cell RNA transcriptome and T-cell repertoire profiles from 14 HCC ascites samples, collected from 7 patients before and after treatment with the combination of sintilimab (anti-PD-1) and bevacizumab (anti-VEGF).

resultsWe identify a widespread convergence on interferon (IFN) signaling across various immune cell lineages in treatment-responsive patients with HCC, indicating a common transcriptional state transition in the immune microenvironment linked to immunotherapy response in HCC. Strong IFN signaling marks CD8

conclusionsThis study provides a unique single-cell resource with clonal and longitudinal resolution during ICI therapy and reveals IFN signaling as a biomarker of immunotherapy response in HCC, suggesting a beneficial effect by combining IFN inducers with ICIs for patients with HCC.

Indexed as

Carcinoma, HepatocellularImmunotherapyInterferonsLiver NeoplasmsTranscriptomeFemaleHumansMaleReceptors, Antigen, T-CellSignal TransductionSingle-Cell AnalysisInterferonsReceptors, Antigen, T-CellHepatocellular CarcinomaImmunotherapy

Identifiers

PMID39581706
PMCPMC11590841

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.