Evidence map›Paper›PMID 32700817›Full record

ArticleCancer medicine2020

TOX correlates with prognosis, immune infiltration, and T cells exhaustion in lung adenocarcinoma.

Longbin Guo, Xuanzi Li, Rongping Liu, Yulei Chen, Chen Ren, Shasha Du

Abstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

33 citing papers in PubMed.

  1. TOX drives CD4Nature immunology · 2026
    Article
  2. Antigen-specific CD8British journal of cancer · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Location of CD39Journal for immunotherapy of cancer · 2023
    Article
  11. Article
  12. Construction of anIranian journal of biotechnology · 2023
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors.

Longbin GuoDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Xuanzi LiDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Rongping LiuDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yulei ChenDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Chen RenDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Shasha DuDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0002-2650-7286

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThymocyte selection-associated high mobility group box (TOX) plays a crucial role on the development of innate immunity and tumor microenvironment. This study aims to explore the prognostic potential of TOX and comprehensively analyze the correlations between TOX, immune infiltration, and T cells function in diverse cancers particularly lung adenocarcinoma (LUAD).

methodsTIMER was used to analyze TOX expression in different cancers. Potential prognostic value of TOX was evaluated by the PrognoScan, Kaplan-Meier Plotter, and GEPIA2. The relationships between TOX, immune infiltration, and related gene marker sets were analyzed by TIMER and GEPIA2. Single-cell RNA-seq for T cells in LUAD was analyzed to further investigate the correlations between TOX expression and different T cells populations.

resultsTOX downregulates in most of the cancer types and correlates with poor prognosis in LUAD. TOX shows significant impacts on survival of LUAD with early stage, ever-smoking, or low-TMB status. Increased TOX expression positively correlates with high immune infiltration levels in most of the immune cells and functional T cells including exhausted T cells. Moreover, multiple key genes of exhausted T cells comprising PD-1, TIM-3, TIGHT, and CXCL13 have remarkable interaction with TOX. Specifically, TOX is observed with high enrichment in exhausted CD4

conclusionTOX is a prognosis-related biomarker for multiple cancer types especially LUAD. Increased TOX expression significantly increase immune infiltration levels in most of the immune cells comprising CD8

Indexed as

Immunogenetic PhenomenaAdenocarcinoma of LungBiomarkers, TumorCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDatabases, Nucleic AcidHigh Mobility Group ProteinsHumansLung NeoplasmsLymphocytes, Tumor-InfiltratingPhenotypePrognosisRNA-SeqTumor MicroenvironmentBiomarkers, TumorHigh Mobility Group ProteinsTOX protein, humanimmune infiltrationimmunotherapylung adenocarcinomaprognosisT cells exhaustionTOX

Identifiers

PMID32700817
PMCPMC7520261

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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.