Evidence map›Paper›PMID 39819441›Full record

ArticleJournal of translational medicine2025

Identification of novel KRAS

Xiaojian Han, Xiaxia Han, Yanan Hao, Bozhi Wang, Luo Li, Siyin Chen, Lin Zou, Jingjing Huang, Tong Chen, Wang Wang and 3 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 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.

  1. Review
  2. 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

13 authors.

Xiaojian Han *Department of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China.
Xiaxia Han *Department of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China.
Yanan HaoDepartment of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China.
Bozhi WangDepartment of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China.
Luo LiDepartment of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China.
Siyin ChenDepartment of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China.
Lin ZouDepartment of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China.
Jingjing HuangDepartment of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China.
Tong ChenDepartment of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China.
Wang WangDepartment of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China.
Shengchun LiuDepartment of Breast and Thyroid Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
Aishun JinDepartment of Immunology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400010, China. aishunjin@cqmu.edu.cn.ORCID 0000-0001-9746-4220
Meiying ShenDepartment of Breast and Thyroid Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China. meiying@hospital.cqmu.edu.cn.

Funding

Chongqing Medical University X4457National Natural Science Foundation of China 81872329National Natural Science Foundation of China 82350120
6 · The paper itself

Abstract

backgroundT cell receptor (TCR)-engineered T cells targeting neoantigens originated from mutations in KRAS gene have demonstrated promising outcomes in clinical trials against solid tumors. However, the challenge lies in developing tumor-specific TCRs that avoid cross-reactivity with self-antigens to minimize the possibility of severe clinical toxicities. Current research efforts have been put towards strategies to eliminate TCR off-target recognition.

methodsNaive T cell repertoire was used for screening KRAS

resultsHLA-A*11:01-restricted TCRs targeting the KRAS

conclusionsTCRs targeting the KRAS

Indexed as

Antigens, NeoplasmProto-Oncogene Proteins p21(ras)Receptors, Antigen, T-CellAmino Acid SequenceHumansJurkat CellsMutationPeptidesT-LymphocytesAntigens, NeoplasmKRAS protein, humanPeptidesProto-Oncogene Proteins p21(ras)Receptors, Antigen, T-CellCross-reactivityKRAS mutationOff-targetT cell receptor

Identifiers

PMID39819441
PMCPMC11740425

What OpenQuestion holds

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Registered trials

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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.