» Articles » PMID: 28576945

The Role of CtBP1 in Oncogenic Processes and Its Potential As a Therapeutic Target

Overview
Journal Mol Cancer Ther
Date 2017 Jun 4
PMID 28576945
Citations 49
Authors
Affiliations
Soon will be listed here.
Abstract

Transcriptional corepressor proteins have emerged as an important facet of cancer etiology. These corepressor proteins are often altered by loss- or gain-of-function mutations, leading to transcriptional imbalance. Thus, research directed at expanding our current understanding of transcriptional corepressors could impact the future development of new cancer diagnostics, prognostics, and therapies. In this review, our current understanding of the CtBP corepressors, and their role in both development and disease, is discussed in detail. Importantly, the role of CtBP1 overexpression in adult tissues in promoting the progression of multiple cancer types through their ability to modulate the transcription of developmental genes ectopically is explored. CtBP1 overexpression is known to be protumorigenic and affects the regulation of gene networks associated with "cancer hallmarks" and malignant behavior, including increased cell survival, proliferation, migration, invasion, and the epithelial-mesenchymal transition. As a transcriptional regulator of broad developmental processes capable of promoting malignant growth in adult tissues, therapeutically targeting the CtBP1 corepressor has the potential to be an effective method for the treatment of diverse tumor types. Although efforts to develop CtBP1 inhibitors are still in the early stages, the current progress and the future perspectives of therapeutically targeting this transcriptional corepressor are also discussed. .

Citing Articles

Identification of novel diagnostic and prognostic microRNAs in sarcoma on TCGA dataset: bioinformatics and machine learning approach.

Rahmati R, Zarimeidani F, Ahmadi F, Yousefi-Koma H, Mohammadnia A, Hajimoradi M Sci Rep. 2025; 15(1):7521.

PMID: 40032929 PMC: 11876432. DOI: 10.1038/s41598-025-91007-x.


Identification of HES4 as a novel prognostic marker and therapeutic target in hepatocellular carcinoma.

Liu Y, Shen Y, Luo P, Wu S, Wang Y, Deng J Discov Oncol. 2025; 16(1):156.

PMID: 39934570 PMC: 11813838. DOI: 10.1007/s12672-025-01915-7.


TOP2A Promotes Proliferation, Migration, and Inflammatory Response in M5-Treated Keratinocytes by Binding CTBP1 to Activate Wnt/β-Catenin Signaling.

Yang Y, Liu S, Xiao X Cell Biochem Biophys. 2024; .

PMID: 39565516 DOI: 10.1007/s12013-024-01620-2.


C-Terminal Binding Protein: Regulator between Viral Infection and Tumorigenesis.

Huang M, Li Y, Li Y, Liu S Viruses. 2024; 16(6).

PMID: 38932279 PMC: 11209466. DOI: 10.3390/v16060988.


PNSC928, a plant-derived compound, specifically disrupts CtBP2-p300 interaction and reduces inflammation in mice with acute respiratory distress syndrome.

Li F, Yan W, Dong W, Chen Z, Chen Z Biol Direct. 2024; 19(1):48.

PMID: 38902802 PMC: 11191317. DOI: 10.1186/s13062-024-00491-0.


References
1.
Deng Y, Liu J, Han G, Lu S, Wang S, Malkoski S . Redox-dependent Brca1 transcriptional regulation by an NADH-sensor CtBP1. Oncogene. 2010; 29(50):6603-8. PMC: 3081720. DOI: 10.1038/onc.2010.406. View

2.
Thio S, Bonventre J, Hsu S . The CtBP2 co-repressor is regulated by NADH-dependent dimerization and possesses a novel N-terminal repression domain. Nucleic Acids Res. 2004; 32(5):1836-47. PMC: 390340. DOI: 10.1093/nar/gkh344. View

3.
Goujon M, McWilliam H, Li W, Valentin F, Squizzato S, Paern J . A new bioinformatics analysis tools framework at EMBL-EBI. Nucleic Acids Res. 2010; 38(Web Server issue):W695-9. PMC: 2896090. DOI: 10.1093/nar/gkq313. View

4.
Kim J, Cho E, Kim S, Youn H . CtBP represses p300-mediated transcriptional activation by direct association with its bromodomain. Nat Struct Mol Biol. 2005; 12(5):423-8. DOI: 10.1038/nsmb924. View

5.
Talbot L, Bhattacharya S, Kuo P . Epithelial-mesenchymal transition, the tumor microenvironment, and metastatic behavior of epithelial malignancies. Int J Biochem Mol Biol. 2012; 3(2):117-36. PMC: 3388731. View