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Overview of Wnt/β-Catenin Pathway and DNA Damage/Repair in Cancer.

作者信息

Nadin Silvina B, Cuello-Carrión F Darío, Cayado-Gutiérrez Niubys, Fanelli Mariel A

机构信息

Laboratorio de Biología Tumoral, Instituto de Medicina y Biología Experimental de Cuyo (IMBECU), Universidad Nacional de Cuyo, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Centro Científico Tecnológico (CCT), Mendoza 5500, Argentina.

Laboratorio de Oncología, IMBECU, CONICET, CCT, Mendoza 5500, Argentina.

出版信息

Biology (Basel). 2025 Feb 11;14(2):185. doi: 10.3390/biology14020185.


DOI:10.3390/biology14020185
PMID:40001953
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11851563/
Abstract

The Wnt/β-catenin pathway takes part in important cellular processes in tumor cells, such as gene expression, adhesion, and survival. The canonical pathway is activated in several tumors, and β-catenin is its major effector. The union of Wnt to the co-receptor complex causes the inhibition of GSK3β activity, thus preventing the phosphorylation and degradation of β-catenin, which accumulates in the cytoplasm, to subsequently be transported to the nucleus to associate with transcription factors. The relationship between Wnt/β-catenin and DNA damage/repair mechanisms has been a focus for the last few years. Studying the Wnt/β-catenin network interactions with DNA damage/repair proteins has become a successful research field. This review provides an overview of the participation of Wnt/β-catenin in DNA damage/repair mechanisms and their future implications as targets for cancer therapy.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/11851563/f2b01aa1fa02/biology-14-00185-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/11851563/3935aed17182/biology-14-00185-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/11851563/1eb2d5b55d3b/biology-14-00185-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/11851563/f2b01aa1fa02/biology-14-00185-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/11851563/3935aed17182/biology-14-00185-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/11851563/1eb2d5b55d3b/biology-14-00185-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/11851563/f2b01aa1fa02/biology-14-00185-g003.jpg

相似文献

[1]
Overview of Wnt/β-Catenin Pathway and DNA Damage/Repair in Cancer.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
The Role of Non-Coding RNAs in the Regulation of Oncogenic Pathways in Breast and Gynaecological Cancers.

Noncoding RNA. 2025-8-6

本文引用的文献

[1]
Wnt Signaling Pathway in Tumor Biology.

Genes (Basel). 2024-12-13

[2]
Novel strategies to overcome chemoresistance in human glioblastoma.

Biochem Pharmacol. 2024-12

[3]
Belling the "cat": Wnt/β-catenin signaling and its significance in future cancer therapies.

Biochim Biophys Acta Rev Cancer. 2024-11

[4]
Molecular dynamics of DNA repair and carcinogen interaction: Implications for cancer initiation, progression, and therapeutic strategies.

Mutat Res. 2024

[5]
Blocking the WNT/β-catenin pathway in cancer treatment:pharmacological targets and drug therapeutic potential.

Heliyon. 2024-8-12

[6]
Exploring the potential of thiophene derivatives as dual inhibitors of β-tubulin and Wnt/β-catenin pathways for gastrointestinal cancers in vitro.

Heliyon. 2024-5-31

[7]
Resveratrol nanoparticles induce apoptosis in oral cancer stem cells by disrupting the interaction between β-catenin and GLI-1 through p53-independent activation of p21.

Med Oncol. 2024-6-4

[8]
The mutagenic consequences of defective DNA repair.

DNA Repair (Amst). 2024-7

[9]
Clinical status and future prospects of neoadjuvant immunotherapy for localized mismatch repair-deficient cancers: a review.

Int J Surg. 2024-9-1

[10]
Multiple functions of HMGB1 in cancer.

Front Oncol. 2024-4-25

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