Evidence map›Paper›PMID 39177262›Full record

ArticleBriefings in bioinformatics2024

BertTCR: a Bert-based deep learning framework for predicting cancer-related immune status based on T cell receptor repertoire.

Min Zhang, Qi Cheng, Zhenyu Wei, Jiayu Xu, Shiwei Wu, Nan Xu, Chengkui Zhao, Lei Yu, Weixing Feng

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. 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
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. 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

9 authors.

Min ZhangCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, No. 145 Nantong Street, Nangang District, Harbin, 150001, China.ORCID 0000-0001-9928-5189
Qi ChengCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, No. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Zhenyu WeiCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, No. 145 Nantong Street, Nangang District, Harbin, 150001, China.ORCID 0009-0001-2950-2560
Jiayu XuCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, No. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Shiwei WuCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, No. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Nan XuInstitute of Biomedical Engineering and Technology, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, No. 500 Dongchuan Road, Shanghai, 200241, China.
Chengkui ZhaoCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, No. 145 Nantong Street, Nangang District, Harbin, 150001, China.ORCID 0000-0002-4328-466X
Lei YuInstitute of Biomedical Engineering and Technology, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, No. 500 Dongchuan Road, Shanghai, 200241, China.
Weixing FengCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, No. 145 Nantong Street, Nangang District, Harbin, 150001, China.

Funding

China National Natural Science Foundation 82073800Natural Science Foundation of Heilongjiang Province of China LH2022F012
6 · The paper itself

Abstract

The T cell receptor (TCR) repertoire is pivotal to the human immune system, and understanding its nuances can significantly enhance our ability to forecast cancer-related immune responses. However, existing methods often overlook the intra- and inter-sequence interactions of T cell receptors (TCRs), limiting the development of sequence-based cancer-related immune status predictions. To address this challenge, we propose BertTCR, an innovative deep learning framework designed to predict cancer-related immune status using TCRs. BertTCR combines a pre-trained protein large language model with deep learning architectures, enabling it to extract deeper contextual information from TCRs. Compared to three state-of-the-art sequence-based methods, BertTCR improves the AUC on an external validation set for thyroid cancer detection by 21 percentage points. Additionally, this model was trained on over 2000 publicly available TCR libraries covering 17 types of cancer and healthy samples, and it has been validated on multiple public external datasets for its ability to distinguish cancer patients from healthy individuals. Furthermore, BertTCR can accurately classify various cancer types and healthy individuals. Overall, BertTCR is the advancing method for cancer-related immune status forecasting based on TCRs, offering promising potential for a wide range of immune status prediction tasks.

Indexed as

Deep LearningNeoplasmsReceptors, Antigen, T-CellComputational BiologyHumansThyroid NeoplasmsReceptors, Antigen, T-Cellcancer-related immune status predictiondeep learningmultiple instance learningpre-trained protein-BERT modelT cell receptor

Identifiers

PMID39177262
PMCPMC11342255

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.