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p53: A player in the tumor microenvironment.

作者信息

Zhao Shuang, Wen Hongyong, Wang Baiqi, Xiong Qinglin, Li Lanxin, Cheng Ailan

机构信息

Hunan Engineering Research Center for Early Diagnosis and Treatment of Liver Cancer, Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang, 421001, China.

The Second Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, 421001, China.

出版信息

Oncol Res. 2025 Mar 19;33(4):795-810. doi: 10.32604/or.2025.057317. eCollection 2025.


DOI:10.32604/or.2025.057317
PMID:40191727
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11964878/
Abstract

Approximately half of all cancers have p53 inactivating mutations, in addition to which most malignancies inactivate the p53 pathway by increasing p53 inhibitors, decreasing p53 activators, or inactivating p53 downstream targets. A growing number of researches have demonstrated that p53 can influence tumor progression through the tumor microenvironment (TME). TME is involved in the process of tumor development and metastasis and affects the clinical prognosis of patients. p53 participates in host immunity and engages in the immune landscape of the TME, but the specific mechanisms remain to be investigated. This review briefly explores the interactions between different states of p53 and TME components and their mechanisms, as well as their effects on tumor progression. To understand the progress of drug development and clinical studies related to p53 and tumor microenvironment.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b61/11964878/fbf2ff990279/OncolRes-33-57317-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b61/11964878/2e94f28f5f06/OncolRes-33-57317-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b61/11964878/fbf2ff990279/OncolRes-33-57317-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b61/11964878/2e94f28f5f06/OncolRes-33-57317-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b61/11964878/fbf2ff990279/OncolRes-33-57317-f002.jpg

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引用本文的文献

[1]
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[2]
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本文引用的文献

[1]
Cell-autonomous IL6ST activation suppresses prostate cancer development via STAT3/ARF/p53-driven senescence and confers an immune-active tumor microenvironment.

Mol Cancer. 2024-10-31

[2]
Unveiling the impact of glutathione (GSH) and gene deletion on tumor cell metabolism by amino acid and proteomics analysis.

J Gastrointest Oncol. 2024-6-30

[3]
Understanding the complexity of p53 in a new era of tumor suppression.

Cancer Cell. 2024-6-10

[4]
Extracellular Matrix Interactome in Modulating Vascular Homeostasis and Remodeling.

Circ Res. 2024-3-29

[5]
miR-146a inhibits ovarian tumor growth via targeting immunosuppressive neutrophils and enhancing CD8 T cell infiltration.

Mol Ther Oncolytics. 2023-9-13

[6]
Is a Novel Target of Mutant p53 in Breast and Ovarian Cancer Cell Lines.

Int J Mol Sci. 2023-9-6

[7]
Cancer immunotherapies: advances and bottlenecks.

Front Immunol. 2023

[8]
Interruption of p53-MDM2 Interaction by Nutlin-3a in Human Lymphoma Cell Models Initiates a Cell-Dependent Global Effect on Transcriptome and Proteome Level.

Cancers (Basel). 2023-7-31

[9]
Acetylation halts missense mutant p53 aggregation and rescues tumor suppression in non-small cell lung cancers.

iScience. 2023-5-30

[10]
Mutant p53 leads to low-grade IFN-I-induced inflammation and impairs cGAS-STING signalling in mice.

Eur J Immunol. 2023-9

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