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癌症中TP53突变背景下TRIM家族预后意义的综合分析

Comprehensive Analysis of the Prognostic Significance of the TRIM Family in the Context of TP53 Mutations in Cancers.

作者信息

Vu Trung, Fowler Annaliese, McCarty Nami

机构信息

Center for Stem Cell and Regenerative Disease, Brown Foundation Institute of Molecular Medicine for the Prevention of Human Diseases (IMM), The University of Texas-Health Science Center at Houston, Houston, TX 77030, USA.

The Department of Biomedical Engineering at Texas A&M University, Houston, TX 77030, USA.

出版信息

Cancers (Basel). 2023 Jul 26;15(15):3792. doi: 10.3390/cancers15153792.

DOI:10.3390/cancers15153792
PMID:37568609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10417774/
Abstract

The p53 protein is an important tumor suppressor, and TP53 mutations are frequently associated with poor prognosis in various cancers. Mutations in TP53 result in a loss of p53 function and enhanced expression of cell cycle genes, contributing to the development and progression of cancer. Meanwhile, several tripartite motif (TRIM) proteins are known to regulate cell growth and cell cycle transition. However, the prognostic values between TP53 and TRIM family genes in cancer are unknown. In this study, we analyzed the relationship between the mutations and TRIM family proteins and evaluated the prognostic significance of TRIM family proteins in cancer patients with P53 mutations. Our findings identified specific TRIM family members that are upregulated in mutant tumors and are associated with the activation of genes related to a cell-cycle progression in the context of TP53 mutations.

摘要

p53蛋白是一种重要的肿瘤抑制因子,TP53突变在多种癌症中常与预后不良相关。TP53突变导致p53功能丧失和细胞周期基因表达增强,促进癌症的发生和发展。同时,已知几种三联基序(TRIM)蛋白可调节细胞生长和细胞周期转换。然而,TP53与TRIM家族基因在癌症中的预后价值尚不清楚。在本研究中,我们分析了TP53突变与TRIM家族蛋白之间的关系,并评估了TRIM家族蛋白在P53突变癌症患者中的预后意义。我们的研究结果确定了在突变肿瘤中上调的特定TRIM家族成员,这些成员在TP53突变的情况下与细胞周期进程相关基因的激活有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/0bca02b24a67/cancers-15-03792-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/cabe388d286e/cancers-15-03792-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/0874590a032a/cancers-15-03792-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/4b18105e33d1/cancers-15-03792-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/6a90ab34e117/cancers-15-03792-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/431e707a21a2/cancers-15-03792-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/d652a1f3d901/cancers-15-03792-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/090bb7f40064/cancers-15-03792-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/29abb34d4e85/cancers-15-03792-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/0bca02b24a67/cancers-15-03792-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/cabe388d286e/cancers-15-03792-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/0874590a032a/cancers-15-03792-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/4b18105e33d1/cancers-15-03792-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/6a90ab34e117/cancers-15-03792-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/431e707a21a2/cancers-15-03792-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/d652a1f3d901/cancers-15-03792-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/090bb7f40064/cancers-15-03792-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/29abb34d4e85/cancers-15-03792-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144d/10417774/0bca02b24a67/cancers-15-03792-g009.jpg

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本文引用的文献

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missense mutations in PDAC are associated with enhanced fibrosis and an immunosuppressive microenvironment.胰腺导管腺癌中的错义突变与增强的纤维化和免疫抑制微环境有关。
肝癌之战:植物源多酚类物质奋起反击。
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TRIM59 promotes tumor growth in hepatocellular carcinoma and regulates the cell cycle by degradation of protein phosphatase 1B.TRIM59 通过降解蛋白磷酸酶 1B 促进肝癌肿瘤生长并调控细胞周期。
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