Evidence map›Paper›PMID 38270700›Full record

ReviewMolecular biology reports2024

TP53 to mediate immune escape in tumor microenvironment: an overview of the research progress.

Kai-Li Zhu, Fei Su, Jing-Ru Yang, Ruo-Wen Xiao, Rui-Yue Wu, Meng-Yue Cao, Xiao-Ling Ling, Tao Zhang

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
6.5field-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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Frontiers in immunology · 2026
    Article
  11. Article
  12. Article
  13. Integrative and deep learning-based prediction of therapy response in ovarian cancer.Journal of experimental & clinical cancer research : CR · 2025
    Article
  14. Interferon Epsilon Loss Is Elusive 9p21 Link to Immune-Cold Tumors, Resistant to Immune Checkpoint Therapy, and Endogenous CXCL9/10 Induction.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2025
    Review
  15. Article
  16. JCO precision oncology · 2025
    Article
  17. Review
  18. Review
  19. Article
  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

8 authors at 2 institutions in 1 country.

Kai-Li Zhu *The First Clinical Medical College of Lanzhou University, Lanzhou, 730000, Gansu, People's Republic of China.
Fei Su *The First Clinical Medical College of Lanzhou University, Lanzhou, 730000, Gansu, People's Republic of China.
Jing-Ru Yang *The First Clinical Medical College of Lanzhou University, Lanzhou, 730000, Gansu, People's Republic of China.
Ruo-Wen XiaoDepartment of Oncology, The First Hospital of Lanzhou University, Lanzhou, 730000, Gansu, People's Republic of China.
Rui-Yue WuThe First Clinical Medical College of Lanzhou University, Lanzhou, 730000, Gansu, People's Republic of China.
Meng-Yue CaoThe First Clinical Medical College of Lanzhou University, Lanzhou, 730000, Gansu, People's Republic of China.
Xiao-Ling LingThe First Clinical Medical College of Lanzhou University, Lanzhou, 730000, Gansu, People's Republic of China. ldyy_lingxl@lzu.edu.cn.
Tao ZhangThe First Clinical Medical College of Lanzhou University, Lanzhou, 730000, Gansu, People's Republic of China. zhangt18@lzu.edu.cn.
First Hospital of Lanzhou University · CNLanzhou University · CN

Funding

Tao Zhang 2022LQTD24Tao Zhang 21JR7RA390Tao Zhang 22YF7FA086Tao Zhang 81802269Tao Zhang 82260518Tao Zhang lzuyxcx-2022-183,2020-ZD-74Xiao-ling Ling 2021SHFZ006Xiao-ling Ling 21JR11R076Xiao-ling Ling cphcf-2022-013
6 · The paper itself

Abstract

Increasing evidence suggests that key cancer-causing driver genes continue to exert a sustained influence on the tumor microenvironment (TME), highlighting the importance of immunotherapeutic targeting of gene mutations in governing tumor progression. TP53 is a prominent tumor suppressor that encodes the p53 protein, which controls the initiation and progression of different tumor types. Wild-type p53 maintains cell homeostasis and genomic instability through complex pathways, and mutant p53 (Mut p53) promotes tumor occurrence and development by regulating the TME. To date, it has been wildly considered that TP53 is able to mediate tumor immune escape. Herein, we summarized the relationship between TP53 gene and tumors, discussed the mechanism of Mut p53 mediated tumor immune escape, and summarized the progress of applying p53 protein in immunotherapy. This study will provide a basic basis for further exploration of therapeutic strategies targeting p53 protein.

Indexed as

NeoplasmsTumor Suppressor Protein p53CognitionGenes, p53Genomic InstabilityHumansTumor MicroenvironmentTP53 protein, humanTumor Suppressor Protein p53Immune escapeImmunotherapyTP53Tumors

Identifiers

PMID38270700
PMCPMC10811008
OpenAlexW4391218035

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.