Literature DB >> 30027840

Signal Transducer and Activator of Transcription Protein 3 (STAT3): An Update on its Direct Inhibitors as Promising Anticancer Agents.

Arianna Gelain1, Matteo Mori1, Fiorella Meneghetti1, Stefania Villa1.   

Abstract

BACKGROUND: Since Signal Transducer and Activator of Transcription 3 (STAT3) is a transcription factor which plays an important role in multiple aspects of cancer, including progression and migration, and it is constitutively activated in various human tumors, STAT3 inhibition has emerged as a validated strategy for the treatment of several malignancies. The aim of this review is to provide an update on the identification of new promising direct inhibitors targeting STAT3 domains, as potential anticancer agents.
METHODS: A thorough literature search focused on recently reported STAT3 direct inhibitors was undertaken. We considered the relevant developments regarding the STAT3 domains, which have been identified as potential drug targets.
RESULTS: In detail, 135 peer-reviewed papers and 7 patents were cited; the inhibitors we took into account targeted the DNA binding domain (compounds were grouped into natural derivatives, small molecules, peptides, aptamers and oligonucleotides), the SH2 binding domain (natural, semi-synthetic and synthetic compounds) and specific residues, like cysteines (natural, semi-synthetic, synthetic compounds and dual inhibitors) and tyrosine 705.
CONCLUSION: The huge number of direct STAT3 inhibitors recently identified demonstrates a strong interest in the investigation of this target, although it represents a challenging task considering that no drug targeting this enzyme is currently available for anticancer therapy. Notably, many studies on the available inhibitors evidenced that some of them possess a dual mechanism of action. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Entities:  

Keywords:  DNA binding domain; SH2 domain; STAT3 direct inhibition; cysteines; naturalzzm321990compound; peptides; semi-synthetic compounds; small molecule.

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Substances:

Year:  2019        PMID: 30027840     DOI: 10.2174/0929867325666180719122729

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  10 in total

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Journal:  Theranostics       Date:  2020-07-02       Impact factor: 11.556

2.  BP‑1‑102 exerts an antitumor effect on the AGS human gastric cancer cell line through modulating the STAT3 and MAPK signaling pathways.

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3.  Brevilin A induces ROS-dependent apoptosis and suppresses STAT3 activation by direct binding in human lung cancer cells.

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6.  Towards the Inhibition of Protein-Protein Interactions (PPIs) in STAT3: Insights into a New Class of Benzothiadiazole Derivatives.

Authors:  Matteo Mori; Ettore Gilardoni; Luca Regazzoni; Alessandro Pedretti; Diego Colombo; Gary Parkinson; Akira Asai; Fiorella Meneghetti; Stefania Villa; Arianna Gelain
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Review 9.  Targeting STAT3 in Cancer Immunotherapy.

Authors:  Sailan Zou; Qiyu Tong; Bowen Liu; Wei Huang; Yan Tian; Xianghui Fu
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10.  Fat mass and obesity-associated protein (FTO) mediates signal transducer and activator of transcription 3 (STAT3)-drived resistance of breast cancer to doxorubicin.

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  10 in total

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