Evidence map›Paper›PMID 38832948›Full record

ArticleCancer immunology, immunotherapy : CII2024

Identification of an HLA-A*11:01-restricted neoepitope of mutant PIK3CA and its specific T cell receptors for cancer immunotherapy targeting hotspot driver mutations.

Meiying Shen, Siyin Chen, Xiaojian Han, Yanan Hao, Junfan Wang, Luo Li, Tong Chen, Bozhi Wang, Lin Zou, Tong Zhang and 7 more

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 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. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Shared neoantigens for cancer immunotherapy.Molecular therapy. Oncology · 2025
    Review
  9. Article
  10. Article
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

17 authors.

Meiying Shen *Department of Breast and Thyroid Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Siyin Chen *Department of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Xiaojian HanDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Yanan HaoDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Junfan WangDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Luo LiDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Tong ChenDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Bozhi WangDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Lin ZouDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Tong ZhangDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Wanli ZhangDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Xiaxia HanDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Wang WangDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
Haochen YuDepartment of Breast and Thyroid Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Kang LiDepartment of Breast and Thyroid Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Shengchun LiuDepartment of Breast and Thyroid Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China. liushengchun1968@163.com.
Aishun JinDepartment of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China. aishunjin@cqmu.edu.cn.

Funding

Chongqing Postdoctoral Science Foundation CSTB2022NSCQ-BHX0636National Natural Science Foundation, China 81872329
6 · The paper itself

Abstract

Hotspot driver mutations presented by human leukocyte antigens might be recognized by anti-tumor T cells. Based on their advantages of tumor-specificity and immunogenicity, neoantigens derived from hotspot mutations, such as PIK3CA

Indexed as

Class I Phosphatidylinositol 3-KinasesMutationNeoplasmsReceptors, Antigen, T-CellAntigens, NeoplasmCD8-Positive T-LymphocytesCell Line, TumorEpitopes, T-LymphocyteHLA-A11 AntigenHumansImmunotherapyAntigens, NeoplasmClass I Phosphatidylinositol 3-KinasesEpitopes, T-LymphocyteHLA-A11 AntigenPIK3CA protein, humanReceptors, Antigen, T-CellAnti-tumor immunotherapyEngineering TCR-THLA-A*11:01NeoantigenPIK3CA

Identifiers

PMID38832948
PMCPMC11150344

What OpenQuestion holds

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LicenceCC BY
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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.