Evidence map›Paper›PMID 35665491›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Hepatobiliary Tumor Organoids Reveal HLA Class I Neoantigen Landscape and Antitumoral Activity of Neoantigen Peptide Enhanced with Immune Checkpoint Inhibitors.

Wenwen Wang, Tinggan Yuan, Lili Ma, Yanjing Zhu, Jinxia Bao, Xiaofang Zhao, Yan Zhao, Yali Zong, Yani Zhang, Shuai Yang and 8 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
7.8field-weighted citation impact, top 2% of its field
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

44 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Review
  3. Human Organoids as a Novel Tool for Vaccine Study.Advanced healthcare materials · 2026
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  15. Review
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  17. State-of-the-Art Liver Cancer Organoids: Modeling Cancer Stem Cell Heterogeneity for Personalized Treatment.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  18. Review
  19. Organoid technology in cervical cancer research.American journal of cancer research · 2025
    Review
  20. 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

18 authors at 7 institutions in 2 countries.

Wenwen WangFudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Tinggan YuanSchool of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
Lili MaSchool of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
Yanjing ZhuThe International Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, 200438, China.
Jinxia BaoSchool of Medicine, Nanjing University, Nanjing, 210093, China.
Xiaofang ZhaoFudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Yan ZhaoInstitute of Metabolism and Integrative Biology, Fudan University, Shanghai, 200433, China.
Yali ZongInstitute of Metabolism and Integrative Biology, Fudan University, Shanghai, 200433, China.
Yani ZhangInstitute of Metabolism and Integrative Biology, Fudan University, Shanghai, 200433, China.
Shuai YangFudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Xinyao QiuFudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Siyun ShenThe International Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, 200438, China.
Rui WuDepartment of Biliary Surgery I, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, 200438, China.
Tong WuThe International Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, 200438, China.
Hongyang WangFudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Dong GaoUniversity of Chinese Academy of Sciences, Beijing, 100049, China.
Peng WangSchool of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
Lei ChenFudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.ORCID 0000-0002-9380-9559
Second Military Medical University · CNFudan University Shanghai Cancer Center · CNFudan University · CNShanghaiTech University · CNChinese Academy of Sciences · CNMinistry of Education of the People's Republic of China · CNNanjing University · CN

Funding

China Postdoctoral Science Foundation 2020M671007Innovation Program of Shanghai Municipal Education Commission 2019-01-07-00-07-E00065National Natural Science Foundation of China 81790633National Natural Science Foundation of China 81830054National Natural Science Foundation of China 81903184National Natural Science Foundation of China 81988101National Natural Science Foundation of China 82102871National Natural Science Foundation of China U21A20376National Science Foundation of Shanghai 21JC1406600National Science Foundation of Shanghai 21XD1404600National Science Foundation of Shanghai 22140901000
6 · The paper itself

Abstract

Neoantigen-directed therapy lacks preclinical models recapitulating neoantigen characteristics of original tumors. It is urgent to develop a platform to assess T cell response for neoantigen screening. Here, immunogenic potential of neoantigen-peptides of tumor tissues and matched organoids (n = 27 pairs) are analyzed by Score tools with whole genome sequencing (WGS)-based human leukocyte antigen (HLA)-class-I algorithms. The comparisons between 9203 predicted neoantigen-peptides from 2449 mutations of tumor tissues and 9991 ones from 2637 mutations of matched organoids demonstrate that organoids preserved majority of genetic features, HLA alleles, and similar neoantigen landscape of original tumors. Higher neoantigen load is observed in tumors with early stage. Multiomics analysis combining WGS, RNA-seq, single-cell RNA-seq, mass spectrometry filters out 93 candidate neoantigen-peptides with strong immunogenic potential for functional validation in five organoids. Immunogenic peptides are defined by inducing increased CD107aCD137IFN-γ expressions and IFN-γ secretion of CD8 cells in flow cytometry and enzyme-linked immunosorbent assay assays. Nine immunogenic peptides shared by at least two individuals are validated, including peptide from TP53

Indexed as

Immune Checkpoint InhibitorsNeoplasmsAntigens, NeoplasmHistocompatibility Antigens Class IHumansOrganoidsPeptidesAntigens, NeoplasmHistocompatibility Antigens Class IImmune Checkpoint InhibitorsPeptidesimmune checkpoint inhibitormultiomics analysisneoantigenpatient derived hepatobiliary tumor organoidTP53

Identifiers

PMID35665491
PMCPMC9353440
OpenAlexW4281722667

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.